http://2012.igem.org/wiki/index.php?title=Special:Contributions/Ymakita&feed=atom&limit=50&target=Ymakita&year=&month=
2012.igem.org - User contributions [en]
2024-03-19T13:31:35Z
From 2012.igem.org
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http://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements
Team:Columbia-Cooper-NYC/Acknowledgements
2012-10-22T21:56:23Z
<p>Ymakita: /* Acknowledgements */</p>
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_2">Genetics</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Safety">Safety</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements">Acknowledgements</a><br />
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<br />
= Acknowledgements =<br />
<br />
Adam Cerini: Copper team, research, Maker Faire<br />
<br />
Marjana Chowdhury: Wiki team, Copper team<br />
<br />
Ciera Lowe: Genetics team, Maker Faire, Wiki team<br />
<br />
Anna Mai: Copper team, Wiki team, Maker Faire<br />
<br />
Yuta Makita: Wiki team, Genetics team, Maker Faire<br />
<br />
Nicholas Mannarino: Genetics team, Maker Faire<br />
<br />
Aakash Mansukhani: Copper team<br />
<br />
Joeseph Mercedes: Copper team, Wiki team<br />
<br />
Steven Neuhaus: Genetics team, research, Wiki team, Maker Faire<br />
<br />
Kirsten Nicassio: Genetics team, research, Wiki team<br />
<br />
Udochukwu (Ud) Okorafor: Copper team, Wiki team, Maker Faire<br />
<br />
Saimon Sharif: Genetics team, research<br />
<br />
Richard Shi: Copper team<br />
<br />
Jeffery Xu: Copper team, Maker Faire<br />
<br />
Vincent Xu: Copper team, Wiki team, Maker Faire<br />
<br />
<br />
<br />
A special thanks to the following iGEM teams and people:<br />
*Dr. Scott Banta for overseeing our project, providing invaluable advice and allowing us to work in his lab at Columbia<br />
*Dr. David Orbach for overseeing our project, consistently generating new ideas or approaches to our goal and allowing us to work in the Kanbar lab at Cooper<br />
*Dionne Lutz for walking the genetic team through countless protocols, supervising our work in the Kanbar lab, helping organize our Maker Faire table and providing much needed motivation and optimism throughout the many failures we faced<br />
*Sudipta Majumdar for helping us construct plasmids and patiently teaching us new protocols<br />
*Kevin Dooley for help with expression experiments, providing us with a GFP gene and identifying and removing cut sights within our biobrick and answering questions as we became acquainted with Dr. Banta's lab<br />
*Tushar Patel for providing us with a GFP gene and answering questions as we became acquainted with Dr. Banta's lab<br />
*Jason Candreva for being extremely patient with us, teaching us various transformation protocols with ecoli and ferrooxidans and answering every question we threw at him<br />
* iGEM Team Uppsala University for sending us the following parts: BBa_K592004, BBa_K592005, BBa_K592006, BBa_K592009, BBa_K592010, and BBa_K592016<br />
* iGEM Team ETH Zurich for sending us E. coli codon-optimized Pif3 and PhyB<br />
* Dr. Nicole Frankenberg-Dinkel for her advice and for sending plasmids pASK-fphAN753s and pTDho1</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements
Team:Columbia-Cooper-NYC/Acknowledgements
2012-10-22T21:56:04Z
<p>Ymakita: </p>
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Team">Biographies</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Facilitators">Facilitators</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Universities">The University(s)</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Future_Directions">Future Directions</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/References">References</a><br />
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<div id="m5" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_2">Genetics</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">Copper Etching</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Protocols">Protocols</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Safety">Safety</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements">Acknowledgements</a><br />
</div><br />
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<br />
= Acknowledgements =<br />
<br />
Adam Cerini: Copper team, research, Maker Faire<br />
<br />
Marjana Chowdhury: Wiki team, Copper team<br />
<br />
Ciera Lowe: Genetics team, Maker Faire captain, Wiki team<br />
<br />
Anna Mai: Copper team, Wiki team, Maker Faire<br />
<br />
Yuta Makita: Wiki team, Genetics team, Maker Faire<br />
<br />
Nicholas Mannarino: Genetics team, Maker Faire<br />
<br />
Aakash Mansukhani: Copper team<br />
<br />
Joeseph Mercedes: Copper team, Wiki team<br />
<br />
Steven Neuhaus: Genetics team, research, Wiki team, Maker Faire<br />
<br />
Kirsten Nicassio: Genetics team, research, Wiki team<br />
<br />
Udochukwu (Ud) Okorafor: Copper team, Wiki team, Maker Faire<br />
<br />
Saimon Sharif: Genetics team, research<br />
<br />
Richard Shi: Copper team<br />
<br />
Jeffery Xu: Copper team, Maker Faire<br />
<br />
Vincent Xu: Copper team, Wiki team, Maker Faire<br />
<br />
<br />
<br />
A special thanks to the following iGEM teams and people:<br />
*Dr. Scott Banta for overseeing our project, providing invaluable advice and allowing us to work in his lab at Columbia<br />
*Dr. David Orbach for overseeing our project, consistently generating new ideas or approaches to our goal and allowing us to work in the Kanbar lab at Cooper<br />
*Dionne Lutz for walking the genetic team through countless protocols, supervising our work in the Kanbar lab, helping organize our Maker Faire table and providing much needed motivation and optimism throughout the many failures we faced<br />
*Sudipta Majumdar for helping us construct plasmids and patiently teaching us new protocols<br />
*Kevin Dooley for help with expression experiments, providing us with a GFP gene and identifying and removing cut sights within our biobrick and answering questions as we became acquainted with Dr. Banta's lab<br />
*Tushar Patel for providing us with a GFP gene and answering questions as we became acquainted with Dr. Banta's lab<br />
*Jason Candreva for being extremely patient with us, teaching us various transformation protocols with ecoli and ferrooxidans and answering every question we threw at him<br />
* iGEM Team Uppsala University for sending us the following parts: BBa_K592004, BBa_K592005, BBa_K592006, BBa_K592009, BBa_K592010, and BBa_K592016<br />
* iGEM Team ETH Zurich for sending us E. coli codon-optimized Pif3 and PhyB<br />
* Dr. Nicole Frankenberg-Dinkel for her advice and for sending plasmids pASK-fphAN753s and pTDho1</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Data_and_Conclusions
Team:Columbia-Cooper-NYC/Data and Conclusions
2012-10-22T21:22:47Z
<p>Ymakita: /* Data and Conclusions */</p>
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Team">Biographies</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Universities">The University(s)</a><br />
<a href="https://igem.org/Team.cgi?year=2012">Official Profile</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Future_Directions">Future Directions</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/References">References</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">Parts Submitted</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_2">Genetics</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">Copper Etching</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Protocols">Protocols</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
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= Data and Conclusions =<br />
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The liquid media that Ferrooxidans thrive in is acidic so the copper team first started working on proving that the bacteria are doing the etching, not just the media. Our initial results were somewhat inconclusive, however the data showed that at certain time intervals the bacteria etched faster than the basal rate (see work from 7/7-7/17 on [https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1 Copper Etching] page under Results):<br />
[[File:table2.png|600px|thumb|center|Figure 1]]<br />
<br />
By furthur refining our experiments as described in the copper notebook we were able to show that copper is in fact etched faster in the presence of A. Ferrooxidans than the basal rate of etching by the acidic liquid media (see the work done 7/18-7/23 on [https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1 Copper Etching] page under Results):<br />
[[File:table1.png|600px|thumb|center|Figure 2]]<br />
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From this data we were able to conclude the following copper consumption rates:<br />
[[File:table3.png|600px|thumb|center|Figure 3]]<br />
<br />
Here is a plot showing the depth etch rate of copper using nail polish as a mean to control etching:<br />
[[File:depth.png|600px|thumb|center|Figure 4]]<br />
<br />
Here is a plot showing the average percent copper lost due solely to the bacteria for different amounts of liquid media on solid media. Note that this doesn't work for the 1 mL case because of the negative %:<br />
[[File:liq_media.png|600px|thumb|center|Figure 5]]<br />
<br />
The Copper team has further refined their experiments by adding more controls and nuances to the existing experiments in order to collect more refined data which is detailed in the notebook, however the major results are summarized here.<br />
<br />
The genetics group has submitted each of the following plasmids to the parts registry:<br />
[[File:plasmid01.png|300px|center]]<br />
.<br />
[[File:plasmid02.png|300px|center]]<br />
.<br />
[[File:plasmid03.png|300px|center]]<br />
.<br />
[[File:plasmid04.png|300px|center]]<br />
.<br />
[[File:plasmid05.png|300px|center]]<br />
.<br />
[[File:plasmid06.png|300px|center]]<br />
.<br />
We plan to characterize parts BBa_K952006 and BBa_K952007 in ecoli.<br />
<br />
[[File:plasmid07.png|300px|center]]<br />
<br />
For BBa_K95006 we can grow the cells in the absence of IPTG, then add the IPTG and shine blue light onto the culture to induce expression of the lysis cassette killing the cells. We will run 2 controls, the first we will add IPTG but keep the cells in the dark and the second we will shine blue light on the cells in the absence of IPTG. Neither of the controls should cause apoptosis while the culture with both promotors present should.<br />
<br />
[[File:plasmid08.png|300px|center]]<br />
<br />
For BBa_K95007 we do not have the addition IPTG promotor present so we will grow the cells in the absence of light, then shine blue light on it to cause cell death. As controls we can attempt to grow the cells in the ambient light of the lab, under red light, and then shine blue light on these cultures if they grow. This is provide information on how sensative the system is to blue light. Ideally the cells would be able to grow in the ambient light of the lab with out inducing cell lysis however we do not expect this to be the case.</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Team
Team:Columbia-Cooper-NYC/Team
2012-10-22T21:18:13Z
<p>Ymakita: </p>
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<br />
<h2>'''Undergraduates'''</h2><br />
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[[Image:Columbia-Cooper-NYC_Team_member_1.jpg|150px|right]]<br />
'''Adam Cerini''': <p>The organism “Adam cerini” is a species of civil engineering student. The Cooper Union is his natural habitat, although he has been observed to migrate to Huntington, NY during the summer months. He appears to have matured to the “sophomore” level. One marked feature of Cerini is his intelligence, a characteristic shared by many species in the engineering family. This feature is suspected to be the cause of his interests in civil engineering, architecture, biochemistry, nanotechnology, environmental science, and biomimicry. Cerini has been shown to undertake complex projects of various types and levels of success, such as mimicking cuttlefish camouflage with LCD’s, constructing a marimba from PVC pipes, designing a bamboo hut for refugees, building an electronic game via breadboards, composing electronic music, and most recently, genetically modifying bacteria for iGEM.</p> <br />
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[[Image:Columbia-Cooper-NYC_Team_member_2.jpg|150px|left]]<br />
'''Marjana Chowdhury''': <p>Despite being from the bustling streets of New York City, Marjana was born to live in the wild. This nature lover and rising sophomore intends to major in Environmental Biology at Columbia University. In the past, Marjana's research has scaled a size spectrum ranging from immense invasive species to minuscule endangered species. As part of the Columbia-Cooper iGEM team, she is excited about her newest and smallest challenge yet, microorganisms.</p><br />
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[[Image:Columbia-Cooper-NYC_Team_member_4.jpg|150px|right]]<br />
'''Ciera Lowe''': <p>Ciera is a rising junior at The Cooper Union majoring in chemical engineering with a minor in biomedical engineering. She joined the iGEM team because this competition provides an amazing opportunity to gain hands on experience in synthetic biology, an exciting field full of potential to improve the world we live in. In addition to her studies, Ciera keeps busy by playing foosball on Cooper’s newly acquired table, playing basketball with Cooper’s women’s team or organizing events with the engineering student council and Cooper’s National Society of Black Engineers chapter.</p><br />
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[[Image:Columbia-Cooper-NYC_Team_member_5.jpg|150px|left]]<br />
'''Anna Mai''': <p>Anna Mai is a rising junior majoring in chemical engineering at Columbia University, with a minor in environmental engineering. She joined IGEM because it presented an interesting medium for interacting with engineers around the world and providing hands on experience in the highly applicable field of synthetic biology. In her spare time she enjoys playing ultimate Frisbee, building paper crafts, and serenading her neighbors (not well).</p><br />
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[[Image:Columbia-Cooper-NYC_Team_member_11.jpg|150px|right]]<br />
'''Yuta Makita''': <p>Yuta Makita is a rising sophomore at the Cooper Union. He is studying Chemical Engineering and has joined the iGEM team with an interest in research based study, the process of synthetic biology and the microscopic world. In addition to his academic studies, he enjoys taking part in orchestra related activities by playing the viola.</p><br />
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[[Image:Columbia-Cooper-NYC_Team_member_6.jpg|150px|left]]<br />
'''Nicholas Mannarino''': <p>Nicholas Mannarino is a rising sophomore at The Cooper Union. He is studying chemical engineering, with a hope to specialize in biomedical engineering and biotechnology. He joined IGEM because it seemed like a great way to spend a summer getting acquainted with a field he is interested in. In his spare time, Nicholas enjoys playing the guitar and long-distance running.</p><br />
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[[Image:Columbia-Cooper-NYC_Team_member_7.jpg|150px|right]]<br />
'''Aakash Mansukhani''': <p>When he’s not obsessively watching American Idol videos or playing tunes on his guitar, Aakash Mansukhani studies chemical engineering at Columbia University. As a rising sophomore, Aakash hopes that participating in IGEM will help him learn more about how principles from chemical engineering and synthetic biology can be combined to program bacteria. In his free time, Aakash loves to sing and reinvent pop songs by putting his own acoustic spin on them.</p><br />
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[[Image:Columbia-Cooper-NYC_Team_member_15.jpg|150px|left]]<br />
'''Joeseph Mercedes''': <p>Joseph Mercedes is a rising sophomore at The Cooper Union. He is majoring in Electrical Engineering. Although iGEM isn’t directly related to his major, it seems like a great opportunity to broaden his knowledge in another field and unify multiple engineering disciplines. In his spare time, Joe enjoys playing tennis and billiards.</p><br />
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[[Image:Columbia-Cooper-NYC_Team_member_8.jpg|150px|right]]<br />
'''Steven Neuhaus''': <p>Steven Neuhaus is a rising sophomore who studies chemical engineering at The Cooper Union for the Advancement of Science and Art. He’s quite fond of the idea of using little things to solve big problems, and joined iGEM because it provides a tremendous opportunity to do just that (and also time to play in the lab!). Steven also enjoys pointing out that writing about oneself in the third person is extremely awkward, is interested in most things that are interesting, and if you show him something cool, he’s usually more than glad to run with it.</p> <br />
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[[Image:Columbia-Cooper-NYC_Team_member_9.jpg|150px|left]]<br />
'''Kirsten Nicassio''': <p>Kirsten Nicassio just finished her freshman year at The Cooper Union. She is majoring in chemical engineering, with an intended math minor. She joined IGEM because of interest in the field of biomedical engineering. In her spare time, Kirsten enjoys reading, knitting, and swimming.</p><br />
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[[Image:Columbia-Cooper-NYC_Team_member_10.jpg|150px|right]]<br />
'''Udochukwu (Ud) Okorafor''': <p>Ud Okorafor is a rising senior at Columbia University. He is majoring in chemical engineering and has interests in protein engineering and pharmaceuticals. He joined IGEM because he enjoyed the research he had done previously on genetic engineering of E. coli. In his spare time, he enjoys playing various sports, reading science fiction books, and watching movies.</p><br />
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[[Image:Columbia-Cooper-NYC_Team_member_12.jpg|150px|left]]<br />
'''Saimon Sharif''': <p>Saimon is a rising sophomore at The Cooper Union. He is studying Chemical Engineering. He joined IGEM because it gives him the opportunity to apply engineering and creativity to biology. In his spare time, Saimon enjoys listening to alternative rock and watching science fiction television shows.</p><br />
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[[Image:Columbia-Cooper-NYC_Team_member_16.jpg|150px|right]]<br />
'''Jeffery Xu''': <p>Jeffrey is a rising sophomore Chemical Engineering student at Cooper and an aspiring chemical/biomedical engineer. He hopes to discover a lot about current research and advancements in the biomedical field, and believes IGEM offers many opportunities to learn from and contribute to. During the (little) time he has when he is not breathing chemistry and understanding the vast enigmas of the applied sciences, he enjoys playing the violin, traveling and catching up with friends.</p><br />
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<br />
<br />
[[Image:Columbia-Cooper-NYC_Team_member_13.png|150px|left]]<br />
'''Vincent Xu''': <p>Vincent is a rising senior at Columbia University majoring in chemical engineering and minoring in applied mathematics. He is more interested in computational modeling than lab work and has been doing research in the applied math department since the summer of his freshman year. He decided to join IGEM because he thinks that it’s a good chance to learn something about biology, which is a subject he hasn’t studied since high school, and to get involved in any computational or modeling work. In addition to enjoying popular activities that college students engage in, such as eating and sleeping, Vincent does ballroom dancing.</p><br />
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<h2>'''High School Students'''</h2><br />
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[[Image:Columbia-Cooper-NYC_Team_member_14.jpg|150px|right]]<br />
'''Richard Shi''': <p>Richard Shi is a high school research student at Jericho High School. He had previously studied and written a paper based on the Dye Sensitized Solar Cell at Farmingdale University. He joined iGEM to vary his exposure to different sciences (moving from the engineering sciences to synthetic biology) and hopes to collect data for the upcoming Intel STS competition. He hopes to bring much to the table, despite being in high school.</p><br />
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Ymakita
http://2012.igem.org/Security
Security
2012-10-04T04:03:16Z
<p>Ymakita: Blanked the page</p>
<hr />
<div></div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements
Team:Columbia-Cooper-NYC/Acknowledgements
2012-10-04T03:58:55Z
<p>Ymakita: </p>
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<br />
= Acknowledgements =<br />
<br />
Adam Cerini: Copper team, research, Maker Faire<br />
<br />
Marjana Chowdhury: Wiki team co-captain, Copper team<br />
<br />
Ciera Lowe: Genetics team, Maker Faire captain, Wiki team<br />
<br />
Anna Mai: Copper team, Wiki team, Maker Faire<br />
<br />
Yuta Makita: Wiki team co-captain, Genetics team<br />
<br />
Nicholas Mannarino: Genetics team<br />
<br />
Aakash Mansukhani: Copper team<br />
<br />
Joeseph Mercedes: Copper team<br />
<br />
Steven Neuhaus: Genetics team co-captain, research, Wiki team<br />
<br />
Kirsten Nicassio: Genetics team co-captain, research, Wiki team<br />
<br />
Udochukwu (Ud) Okorafor: Copper team, Wiki team, Maker Faire<br />
<br />
Saimon Sharif: Genetics team co-captain, research<br />
<br />
Richard Shi: Copper team<br />
<br />
Jeffery Xu: Copper team<br />
<br />
Vincent Xu: Copper team captain, Wiki team, Maker Faire<br />
<br />
<br />
<br />
A special thanks to the following iGEM teams and people:<br />
*Dr. Scott Banta for overseeing our project, providing invaluable advice and allowing us to work in his lab at Columbia<br />
*Dr. David Orbach for over seeing our project, consistently generating new ideas or approaches to our goal and allowing us to work in the Kanbar lab at Cooper<br />
*Dionne Lutz for walking the genetic team through countless protocols, supervising our work in the Kanbar lab, helping organize our Maker Faire table and providing much needed motivation and optimism throughout the many failures we faced<br />
*Sudipta Majumdar for helping us construct plasmids and patiently teaching us new protocols<br />
*Kevin Dooley for help with expression experiments, providing us with a GFP gene and identifying and removing cut sights within our biobrick and answering questions as we became acquainted with Dr. Banta's lab<br />
*Tushar Patel for providing us with a GFP gene and answering questions as we became acquainted with Dr. Banta's lab<br />
*Jason Candreva for being extremely patient with us, teaching us various transformation protocols with ecoli and ferrooxidans and answering every question we threw at him<br />
* iGEM Team Uppsala University for sending us the following parts: BBa_K592004, BBa_K592005, BBa_K592006, BBa_K592009, BBa_K592010, and BBa_K592016<br />
* iGEM Team ETH Zurich for sending us E. coli codon-optimized Pif3 and PhyB<br />
* Dr. Nicole Frankenberg-Dinkel for her advice and for sending plasmids pASK-fphAN753s and pTDho1</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Ligation
Team:Columbia-Cooper-NYC/Ligation
2012-10-04T03:42:42Z
<p>Ymakita: </p>
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<br />
= Ligation Protocol for 3A Assembly Method =<br />
* The following protocol is provided by bioworks:<br />
# Add 11µl of denionized water to 200µl PCR tube<br />
# Add 2µl of each of the digests to the tube<br />
# Add 2µl of 10X T4 DNA Ligase Reaction Buffer to tube<br />
# Add 1µl of the T4 DNA Ligase to the tube<br />
# Mix solution well<br />
# Incubate the reaction mix at room temperature for 10 minutes<br />
# Incubate the reaction mix at 80C for 20 minutes to inactivate enzymes<br />
# Store ligation mix at -20C<br />
<br />
Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]]</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Digestion
Team:Columbia-Cooper-NYC/Digestion
2012-10-04T03:42:19Z
<p>Ymakita: </p>
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<br />
= Digestion Protocol for 3A Assembly Method =<br />
* The following was protocol provided by bioworks:<br />
# Determine upstream part, downstream part and destination plasmid<br />
# Label three PCR tubes as U, D, P respectively<br />
# To each tube add 500ng of plasmid to be digested <br />
# Add necessary amount of water so final volume is 42.5µl<br />
# Add 5µl of NEBuffer 2 to each tube<br />
# Add 0.5µl of BSA to each tube<br />
# Add 1µl of first appropriate enzyme<br />
# Add 1µl of second appropriate enzyme<br />
# Ensure that digest is well mixed<br />
# Incubate the digests at 37C for 15 minutes in thermocycler<br />
# Incubate the digests at 80C for 20 minutes to deactivate the restriction enzymes<br />
# Store digest at -20C<br />
<br />
Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]]</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Plates
Team:Columbia-Cooper-NYC/Plates
2012-10-04T03:41:55Z
<p>Ymakita: </p>
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= Protocol for Creating Plates =<br />
* The following is the protocol for creating plates to grow bacteria on:<br />
# Prepare 1L bottle<br />
# For 500mL, add 7.5g of agar and 12.5g of LB<br />
# Pour deionized water until water level reaches 500mL<br />
# Cover bottle with foil and tape with autoclave tape<br />
# Autoclave on slow for 20 minutes<br />
# After autoclaving, let bottle stand cool until touch<br />
# Apply 500µl of 1000x stock antibiotics to make 1x solution<br />
# Pour solution into plates<br />
<br />
Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]]</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Electroporation
Team:Columbia-Cooper-NYC/Electroporation
2012-10-04T03:41:36Z
<p>Ymakita: </p>
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<br />
= Electroporation Protocol =<br />
* The following is the electroporation protocol provided by bioline:<br />
# Place cuvettes and competent cells into ice<br />
# Add 1µl of DNA to 50µl of competent cells into 1mL cuvettes as quickly as possible<br />
# Keep cuvettes in ice until electroporation<br />
# Electroporate cells at 1800V<br />
# Place bacteria back into tube and add 100-200µl of LB<br />
# Place samples in shaker for 37C for 1 hour<br />
<br />
Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]]</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Miniprep
Team:Columbia-Cooper-NYC/Miniprep
2012-10-04T03:41:10Z
<p>Ymakita: </p>
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<div id="m9" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
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<!-- /dd --><br />
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<br />
= Plasmid Isolation Protocol =<br />
* Following is a plasmid isolation protocol provided by QIAGEN:<br />
# Resuspend pelleted bacterial cells in 250µl Buffer P1 and transfer to a microcentrifuge tube<br />
# Add 250µl Buffer P2 and mix thoroughly by inverting the tube 4-6 times<br />
# Add 350µl Buffer N3 and mix immediately and thoroughly by inverting the tube 4-6 times<br />
# Centrifuge for 10 min. at 13,000 rpm in a table-top microcentrifuge<br />
# Apply the supernatant (from step 4) to the QIAprep spin column by decanting<br />
# Centrifuge for 30-60 seconds and discard the flow-through<br />
# Wash QIAspin column by adding 0.75ml Buffer PE and centrifuging for 30-60 seconds<br />
# Discard the flow-through, and centrifuge for an additional 1-3 minutes to remove residual wash buffer<br />
# To elute DNA, place the QIAprep column in a clean 1.5ml microcentrifuge tube. Add 50µl water to center of QIAprep spin column, let stand for 1 minute and centrifuge for 1-3 minutes.<br />
<br />
Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]]</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Rehydration
Team:Columbia-Cooper-NYC/Rehydration
2012-10-04T03:40:50Z
<p>Ymakita: </p>
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements">Acknowledgements</a><br />
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<div id="m9" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
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<!-- /dd --><br />
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</head><br />
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<br />
= iGEM Biobrick Rehydration Protocol =<br />
* The following is the protocol for rehydrating DNA provided by iGEM:<br />
# Determine the location of well on specific plate<br />
# Punch a hole into well using pipette<br />
# Add 10µl of deionized water and mix<br />
# Store sample in freezer at -20°C<br />
<br />
Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]]</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Primers
Team:Columbia-Cooper-NYC/Primers
2012-10-04T03:40:33Z
<p>Ymakita: </p>
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body{background-image:url('http://farm9.staticflickr.com/8173/7989724336_9e5441e3ff_b.jpg');<br />
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{ display: block;<br />
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text-align: center;<br />
text-decoration: none}<br />
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#sddm li a:hover<br />
{ background: #B87333}<br />
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{ position: relative;<br />
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<!-- div class="sample" style="margin-bottom: 15px;height:42px;"><span --><br />
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</li><br />
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<div id="m5" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_2">Genetics</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">Copper Etching</a><br />
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</div><br />
</li><br />
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<div id="m8" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements">Acknowledgements</a><br />
</div><br />
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<div id="m9" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
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<!-- /dd --><br />
</script><br />
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</head><br />
</html><br />
<br />
= Preparation of Primer Stock Protocol =<br />
* Protocol for preparing the concentrated primers to be able to be used in DNA sequencing is the following:<br />
*# Add 20x primer weight of deionized water to concentrated primer <br />
*# Vortex 20 seconds of sample with concentrated primer and deionized water<br />
*# Centrifuge for 10 seconds of the sample<br />
*# Diluted sample 100x again for use as stock<br />
<br />
Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]]</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Gel_Electrophoresis_Setup
Team:Columbia-Cooper-NYC/Gel Electrophoresis Setup
2012-10-04T03:40:11Z
<p>Ymakita: </p>
<hr />
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<style type="text/css"><br />
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background-position:top left;<br />
background-repeat:repeat-y<br />
<br />
body{background-image:url('http://farm9.staticflickr.com/8173/7989724336_9e5441e3ff_b.jpg');<br />
background-position:top right;<br />
background-repeat:repeat-y<br />
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= Gel Electrophoresis Setup and Run Protocol =<br />
''Note: The protocol is for creating 60ml of 1% agar gel used to run small DNA sequences of several hundred''<br />
<br />
''To run gels for larger sequences (using the corresponding ladder), create a .7% agar gel''<br />
# Measure .6g of ultra pure agar<br />
# Suspend agar in 60ml of TAE buffer<br />
# Place cap on bottle containing the solution<br />
# Set microwave for 120 seconds, let solution heat in microwave for first 45 seconds<br />
# Take out bottle and shake bottle and place back in microwave<br />
# Repeat step 5 every 10-15 seconds there after<br />
# After microwaving let solution stand to cool in hood ''Note: Do not let gel solidify''<br />
# While cooling, rinse the gel mold with deionized water and make sure rubber gaskets are air tight and in place<br />
# Place well molds in place<br />
# Add .8µl Ethiolium bromide to TAE/agar mixture<br />
# Pour the mixture into mold and let it stand until hardens<br />
To run the gels:<br />
# Gently remove wells from hardened gel<br />
# For every 5µl of DNA add 1µl of 6x loading dye ''Note: Need to add loading dye to each sample of DNA)<br />
# Add 7-8µl of 2 log ladder in first column<br />
# Place desired DNA for inspection in all the other columns<br />
# Run gel at steady 150V<br />
Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]]</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Chemical_Transformation
Team:Columbia-Cooper-NYC/Chemical Transformation
2012-10-04T03:39:44Z
<p>Ymakita: </p>
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= Chemical Transformation/Heat Shock Protocol from Bioline =<br />
# Remove and thaw chemically competent cells<br />
# Aliquot 1-5µl DNA per 40-50µl of competent cells<br />
# Incubate on ice for 30 minutes<br />
# Heat shock cells for 45 seconds at 42°C<br />
# Let cells stand on ice for 2 minutes<br />
# Place cells in growth media and let it stand for 1 hour<br />
# Plate cells on appropriate antibiotic and add IPTG when appropriate<br />
Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]]</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/OD_Measurement
Team:Columbia-Cooper-NYC/OD Measurement
2012-10-04T03:38:57Z
<p>Ymakita: </p>
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements">Acknowledgements</a><br />
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<!-- /dd --><br />
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</head><br />
</html><br />
<br />
= Optical Density Measurement Protocol =<br />
# Preset temperature and wavelength for measuring the optical density<br />
# Read and reference 1mL control solution (e.g. if E. coli was grown in LB/CAM) placed in disposable cuvette<br />
# Place 10µl cells into 1mL solution<br />
# Read the absorbance<br />
''Make note that when reading the optical density, must be referenced by a reference solution''<br />
<br />
Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]]</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Making_Liquid_Media
Team:Columbia-Cooper-NYC/Making Liquid Media
2012-10-04T03:38:33Z
<p>Ymakita: </p>
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<br />
== Liquid Media Protocol ==<br />
<br />
For 1 liter of liquid media: <br />
<OL><br />
<LI>Combine in a large beaker, while stirring with a magnetic bar:<br />
<UL><br />
<LI>1 L of distilled water<br />
<LI>0.8 g of ammonium sulfate (NH4)2SO4<br />
<LI>1.0 g of magnesium sulfate MgSO4<br />
<LI>0.4 g of dipotassium phosphate K2HPO4<br />
<LI>5.0 mL o MD-TMS<br />
</UL><br />
<LI>Using sulfuric acid (H2PO4), adjust pH of solution to 2.1. This should take about 0.5 mL of H2PO4<br />
<LI>Add 20 g of FeSO4.7H20<br />
<LI>Using sulfuric acid, adjust pH of solution to 1.8-1.85<br />
<LI>Once solution appears homogeneous, filter sterilize<br />
</OL><br />
<br />
<i>Credit for protocol goes to Jason Candreva, Research Associate, Columbia University</i><br />
<br />
Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]]</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Making_Solid_Media
Team:Columbia-Cooper-NYC/Making Solid Media
2012-10-04T03:38:18Z
<p>Ymakita: </p>
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== Solid Media Protocol ==<br />
<br />
<br />
<br />
<i>Credit for protocol goes to Jason Candreva, Research Associate, Columbia University</i><br />
<br />
Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]]</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Making_Solid_Media
Team:Columbia-Cooper-NYC/Making Solid Media
2012-10-04T03:37:40Z
<p>Ymakita: </p>
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<div id="m4" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">Parts Submitted</a><br />
</div><br />
</li><br />
<li><a href="#" onmouseover="mopen('m5')" onmouseout="mclosetime()">Lab Notebook</a><br />
<div id="m5" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_2">Genetics</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">Copper Etching</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Protocols">Protocols</a><br />
</div><br />
</li><br />
<li><a href="#" onmouseover="mopen('m6')" onmouseout="mclosetime()">Human Practice</a><br />
<div id="m6" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">Outreach</a><br />
</div><br />
</li><br />
<li><a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Safety" onmouseover="mopen('m7')" onmouseout="mclosetime()">Safety</a><br />
<div id="m7" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Safety">Safety</a><br />
</div><br />
</li><br />
<li><a href="#" onmouseover="mopen('m8')" onmouseout="mclosetime()">Sponsors</a><br />
<div id="m8" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements">Acknowledgements</a><br />
</div><br />
</li><br />
<li><a href="https://2012.igem.org/Main_Page" onmouseover="mopen('m9')" onmouseout="mclosetime()">iGEM</a><br />
<div id="m9" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
</div><br />
</li><br />
</ul><br />
<div style="clear:both"></div><br />
<!-- /span></div --><br />
<!-- /dd --><br />
</script><br />
</body><br />
</head><br />
</html><br />
== Solid Media Protocol ==<br />
<br />
<br />
<br />
<i>Credit for protocol goes to Jason Candreva, Research Associate, Columbia University</i></div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Making_Liquid_Media
Team:Columbia-Cooper-NYC/Making Liquid Media
2012-10-04T03:37:07Z
<p>Ymakita: </p>
<hr />
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<div id="m2" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Team">Biographies</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Universities">The University(s)</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Future_Directions">Future Directions</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/References">References</a><br />
</div><br />
</li><br />
<li><a href="#" onmouseover="mopen('m4')" onmouseout="mclosetime()">Parts</a><br />
<div id="m4" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">Parts Submitted</a><br />
</div><br />
</li><br />
<li><a href="#" onmouseover="mopen('m5')" onmouseout="mclosetime()">Lab Notebook</a><br />
<div id="m5" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_2">Genetics</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">Copper Etching</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Protocols">Protocols</a><br />
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<div id="m6" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">Outreach</a><br />
</div><br />
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<div id="m7" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Safety">Safety</a><br />
</div><br />
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<div id="m8" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements">Acknowledgements</a><br />
</div><br />
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<li><a href="https://2012.igem.org/Main_Page" onmouseover="mopen('m9')" onmouseout="mclosetime()">iGEM</a><br />
<div id="m9" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
</div><br />
</li><br />
</ul><br />
<div style="clear:both"></div><br />
<!-- /span></div --><br />
<!-- /dd --><br />
</script><br />
</body><br />
</head><br />
</html><br />
<br />
== Liquid Media Protocol ==<br />
<br />
For 1 liter of liquid media: <br />
<OL><br />
<LI>Combine in a large beaker, while stirring with a magnetic bar:<br />
<UL><br />
<LI>1 L of distilled water<br />
<LI>0.8 g of ammonium sulfate (NH4)2SO4<br />
<LI>1.0 g of magnesium sulfate MgSO4<br />
<LI>0.4 g of dipotassium phosphate K2HPO4<br />
<LI>5.0 mL o MD-TMS<br />
</UL><br />
<LI>Using sulfuric acid (H2PO4), adjust pH of solution to 2.1. This should take about 0.5 mL of H2PO4<br />
<LI>Add 20 g of FeSO4.7H20<br />
<LI>Using sulfuric acid, adjust pH of solution to 1.8-1.85<br />
<LI>Once solution appears homogeneous, filter sterilize<br />
</OL><br />
<br />
<i>Credit for protocol goes to Jason Candreva, Research Associate, Columbia University</i></div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Making_Liquid_Media
Team:Columbia-Cooper-NYC/Making Liquid Media
2012-10-04T03:36:05Z
<p>Ymakita: </p>
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Team">Biographies</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Universities">The University(s)</a><br />
<a href="https://igem.org/Team.cgi?year=2012">Official Profile</a><br />
</div><br />
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<li><a href="#" onmouseover="mopen('m3')" onmouseout="mclosetime()">Project</a><br />
<div id="m3" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">Overview</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Data_and_Conclusions">Data and Conclusions</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Future_Directions">Future Directions</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/References">References</a><br />
</div><br />
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<li><a href="#" onmouseover="mopen('m4')" onmouseout="mclosetime()">Parts</a><br />
<div id="m4" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">Parts Submitted</a><br />
</div><br />
</li><br />
<li><a href="#" onmouseover="mopen('m5')" onmouseout="mclosetime()">Lab Notebook</a><br />
<div id="m5" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_2">Genetics</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">Copper Etching</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Protocols">Protocols</a><br />
</div><br />
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<li><a href="#" onmouseover="mopen('m6')" onmouseout="mclosetime()">Human Practice</a><br />
<div id="m6" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">Outreach</a><br />
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<div id="m7" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Safety">Safety</a><br />
</div><br />
</li><br />
<li><a href="#" onmouseover="mopen('m8')" onmouseout="mclosetime()">Sponsors</a><br />
<div id="m8" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements">Acknowledgements</a><br />
</div><br />
</li><br />
<li><a href="https://2012.igem.org/Main_Page" onmouseover="mopen('m9')" onmouseout="mclosetime()">iGEM</a><br />
<div id="m9" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
</div><br />
</li><br />
</ul><br />
<div style="clear:both"></div><br />
<!-- /span></div --><br />
<!-- /dd --><br />
</script><br />
</body><br />
</head><br />
</html><br />
<br />
== Liquid Media Protocol ==<br />
<br />
For 1 liter of liquid media: <br />
<OL><br />
<LI>Combine in a large beaker, while stirring with a magnetic bar:<br />
<UL><br />
<LI>1 L of distilled water<br />
<LI>0.8 g of ammonium sulfate (NH4)2SO4<br />
<LI>1.0 g of magnesium sulfate MgSO4<br />
<LI>0.4 g of dipotassium phosphate K2HPO4<br />
<LI>5.0 mL o MD-TMS<br />
</UL><br />
<LI>Using sulfuric acid (H2PO4), adjust pH of solution to 2.1. This should take about 0.5 mL of H2PO4<br />
<LI>Add 20 g of FeSO4.7H20<br />
<LI>Using sulfuric acid, adjust pH of solution to 1.8-1.85<br />
<LI>Once solution appears homogeneous, filter sterilize<br />
</OL><br />
<br />
<i>Credit for protocol goes to Jason Candreva, Research Associate, Columbia University</i></div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted
Team:Columbia-Cooper-NYC/Parts Submitted
2012-10-04T02:22:43Z
<p>Ymakita: </p>
<hr />
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<div id="m2" onmouseover="mcancelclosetime()" onmouseout="mclosetime()"><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Universities">The University(s)</a><br />
<a href="https://igem.org/Team.cgi?year=2012">Official Profile</a><br />
</div><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Future_Directions">Future Directions</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/References">References</a><br />
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= Parts Submitted =<br />
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<td>IPTG inducible promoter-B0034-YF1-B0034-FixJ </td><br />
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<br />
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= Future Parts =<br />
<html><br />
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<tr><br />
<td><a href="http://partsregistry.org/Part:BBa_K952006">BBa_K952006</a></td><br />
<td>Composite</td><br />
<td>const. promoter-B0034-YF1-B0034-FixJ-PfixK2-Lysis Cassette </td><br />
</tr><br />
<tr><br />
<td><a href="http://partsregistry.org/Part:BBa_K952007">BBa_K952007</a></td><br />
<td>Composite</td><br />
<td>IPTG induc. promoter-B0034-YF1-B0034-FixJ-PfixK2-Lysis Cassette</td><br />
</tr><br />
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<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-04T02:19:15Z
<p>Ymakita: </p>
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Columbia & Cooper 2012 Team</h2><br />
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Copper Etching</h2><br />
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<div style="width:950px; background-color:#5C3317;" class="secheader">The Project</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<div id="lefttop" style="background:#B87333; background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png');" class="secheader">iGEM</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<div id="ctop" style="background:#238E23;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Genetics</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
<div id="ccontent" style="background:-webkit-gradient(linear, left top, left bottom, from(#f2f2f2), to(#f8f8f8)); <br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, the bacteria A. ferrooxidans. Using our liquid media, we were able to grow ferrooxidans and simultaneously etch copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
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<div id="leftbox" style="float:left; height:250px; width:316px;" class="tophome"><br />
<div id="lefttop" style="background:#238E23; background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png');" class="secheader">Biobrick</div><br />
<div id="leftcontent" style="background:-webkit-gradient(linear, left top, left bottom, from(#f2f2f2), to(#f8f8f8)); <br />
background: -moz-linear-gradient(top, #f2f2f2, #f8f8f8); color:#333333; height:250px;"><br />
<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
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<a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">here</a> for a full list of our submitted parts.</p><br />
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<div id="ctop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Outreach</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Universities
Team:Columbia-Cooper-NYC/Universities
2012-10-04T00:18:27Z
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Team">Biographies</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">Copper Etching</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Protocols">Protocols</a><br />
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= '''[http://www.columbia.edu Columbia University]''' =<br />
<br />
[[Image:Columbia-Cooper-NYC_Alma_Mater.jpg|center|link=http://www.columbia.edu]]<br />
<br />
Columbia University is a distinctive and distinguished learning environment for undergraduates and graduate students in many professional fields. As part of the Ivy League and because of its location in New York City, it attracts a diverse faculty and student body from all over the world. With many research opportunities available for students, several undergraduates from Columbia University have partnered with students at The Cooper Union to work on a synthetic biology competition (iGEM) over the summer of 2012. Under the help and supervision of Scott A. Banta, an associate professor in the department of Chemical Engineering in The Fu Foundation School of Engineering and Applied Science, the undergraduates were able to work in his lab over the summer and receive funding for their project.<br />
<br />
= '''[http://www.cooper.edu The Cooper Union for the Advancement of Science and Art]''' =<br />
<br />
[[Image:Cooperwiki.jpg|center|link=http://www.cooper.edu]]<br />
<br />
The majority of the members of this team are "ChemE" undergraduates at the '''Cooper Union'''. Cooper, located in East Village, Manhattan, is a small college (less than 300 students per grade), highly selective (acceptance rates are near 8%), and contains 3 schools: Art, Architecture, and Engineering. Within the engineering school are five majors: Chemical, civil, electrical, mechanical (these four are ABET-accredited B.E.'s), and B.S.E. (meant for those who wish to practice in a field related to engineering, like patent law or medicine). Since Peter Cooper founded the college in 1859, all undergraduates have and continue to receive a full-tuition scholarship upon attending. Adjunct professor David Orbach, who teaches biology courses at Cooper, set up both this year's and last year's iGEM team. Technician Dionne Lutz operates a lab at Cooper called the "Kanbar Center for Biomedical Engineering" and provided both her expertise and the lab for our team's use.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach
Team:Columbia-Cooper-NYC/Outreach
2012-10-04T00:05:06Z
<p>Ymakita: </p>
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<br />
= Outreach =<br />
[[File:Maker7.gif|600px|thumb|center|Our table at Maker Faire NYC 2012]]<br />
<br />
<br />
<br />
<br />
[[File:penny.jpg|100px|thumb|left|Normal Penny]][[File:Etched Penny.jpg|100px|thumb|left|A Penny Etched by Ferrooxidans]][[File:Source Cells.jpg|115px|thumb|right|Our Source Cells]] [[File:Electroporation.jpg|115px|thumb|right|Our Electroporation Game]] <br />
This year Columbia- Cooper iGEM hosted a table at the 2012 Maker Faire in New York City. Our table featured posters explaining both the genetic and chemical aspects of out project, games to teach children about recombinant DNA and bacterial transformation as well as pennies etched by our A. Ferrooxidans with the letter "C" to represent each of our schools as well as the chemical symbol for copper.<br />
<br />
Each of our games contained plastic spheres which represented cells and a strip of blue, yellow and orange DNA. We explained to the kids that we took DNA out of our source cells, cut out the parts we wanted and put them back together in a new combination. Now we need the kids help to put our new DNA into a cell so it can be used. In the conjugation game the 2 cells were connected by a plastic tube and the goal was to move the DNA from one cell to the other. In the electroporation game the kids used a wand with a magnet on the end to slide the recombinant DNA through one of the large pores into our cell. As the kids worked on the game we had a chance to explain to their parents that in the lab we do this by shocking the cells with 1800 volts. Finally our chemical transformation game involved throwing the DNA into our competent cells. In order to help keep the DNA in the cell rather than sliding right out we attached a small magnet to the bottom on the DNA and put a piece of metal between the cell and the base.<br />
[[File:Chemical Transfomration.jpg|150px|thumb|left|Our Chemical Transformation Game]][[File:conjugation.jpg|150px|thumb|center|Our Conjugation Game]]<br />
<br />
[[File:Maker2.gif|225px|left| ]] [[File:Maker3.gif|225px|center| ]]<br />
<br />
<br />
Thank you to everyone who stopped by our booth! Our team appreciated the opportunity to share the work we've done as well as everyone who wished us luck over the next few weeks as we complete our project.</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-03T14:39:34Z
<p>Ymakita: </p>
<hr />
<div><div style="text-align: right;" class="top-links">[https://igem.org/Login Login] [https://igem.org/Logout Logout]<br />
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[https://2012.igem.org/wiki/index.php?title=Team:Columbia-Cooper-NYC/Main&action=edit edit] <br />
[https://2012.igem.org/wiki/index.php?title=Team:Columbia-Cooper-NYC/Main&action=history history]<br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Team">Biographies</a><br />
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Columbia & Cooper 2012 Team</h2><br />
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The Cooper Union for the Advancement of Science and Art</h2><br />
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Copper Etching</h2><br />
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The Effects of A. ferrooxidans</h2><br />
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<div style="width:950px; background-color:#5C3317;" class="secheader">The Project</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<div id="ctop" style="background:#238E23;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Genetics</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, ferrooxidans (the bacteria), and other chemicals. Using our liquid media, we were able to grow healthy ferrooxidans and simultaneously dissolve (etch) copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. We have utilized nail polish as a varnish to control the etching until the genetics group completes our biological controled etching mechanism. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-03T14:37:24Z
<p>Ymakita: </p>
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
<div id="ccontent" style="background:-webkit-gradient(linear, left top, left bottom, from(#f2f2f2), to(#f8f8f8)); <br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, ferrooxidans (the bacteria), and other chemicals. Using our liquid media, we were able to grow healthy ferrooxidans and simultaneously dissolve (etch) copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. We have utilized nail polish as a varnish to control the etching until the genetics group completes our biological controled etching mechanism. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
<br />
<a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">here</a> for a full list of our submitted parts.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-03T14:36:49Z
<p>Ymakita: </p>
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<li><a href="https://2012.igem.org/Team:Columbia-Cooper-NYC" onmouseover="mopen('m1')" onmouseout="mclosetime()">Home</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Team">Biographies</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Universities">The University(s)</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Future_Directions">Future Directions</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/References">References</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_2">Genetics</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements">Acknowledgements</a><br />
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Columbia & Cooper 2012 Team</h2><br />
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The Cooper Union for the Advancement of Science and Art</h2><br />
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Copper Etching</h2><br />
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The Effects of A. ferrooxidans</h2><br />
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<div style="width:950px; background-color:#5C3317;" class="secheader">The Project</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<div id="ctop" style="background:#238E23;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Genetics</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, ferrooxidans (the bacteria), and other chemicals. Using our liquid media, we were able to grow healthy ferrooxidans and simultaneously dissolve (etch) copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. We have utilized nail polish as a varnish to control the etching until the genetics group completes our biological controled etching mechanism. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
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<a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">here</a> for a full list of our submitted parts.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-03T14:35:11Z
<p>Ymakita: </p>
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<div style="width:950px; background-color:#5C3317;" class="secheader">The Project</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<div id="ctop" style="background:#238E23;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Genetics</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, ferrooxidans (the bacteria), and other chemicals. Using our liquid media, we were able to grow healthy ferrooxidans and simultaneously dissolve (etch) copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. We have utilized nail polish as a varnish to control the etching until the genetics group completes our biological controled etching mechanism. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
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<a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">here</a> for a full list of our submitted parts.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-03T14:33:00Z
<p>Ymakita: </p>
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<li><a href="https://2012.igem.org/Team:Columbia-Cooper-NYC" onmouseover="mopen('m1')" onmouseout="mclosetime()">Home</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Team">Biographies</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_2">Genetics</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
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Columbia & Cooper 2012 Team</h2><br />
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The Effects of A. ferrooxidans</h2><br />
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<div style="width:950px; background-color:#5C3317;" class="secheader">The Project</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<div id="ctop" style="background:#238E23;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Genetics</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, ferrooxidans (the bacteria), and other chemicals. Using our liquid media, we were able to grow healthy ferrooxidans and simultaneously dissolve (etch) copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. We have utilized nail polish as a varnish to control the etching until the genetics group completes our biological controled etching mechanism. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
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<a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">here</a> for a full list of our submitted parts.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-03T14:28:50Z
<p>Ymakita: </p>
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<div style="width:950px; background-color:#5C3317;" class="secheader">The Project</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<div id="lefttop" style="background:#B87333; background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png');" class="secheader">iGEM</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<div id="ctop" style="background:#238E23;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Genetics</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, ferrooxidans (the bacteria), and other chemicals. Using our liquid media, we were able to grow healthy ferrooxidans and simultaneously dissolve (etch) copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. We have utilized nail polish as a varnish to control the etching until the genetics group completes our biological controled etching mechanism. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
<br />
<a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">here</a> for a full list of our submitted parts.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-03T14:27:37Z
<p>Ymakita: </p>
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<li><a href="https://2012.igem.org/Team:Columbia-Cooper-NYC" onmouseover="mopen('m1')" onmouseout="mclosetime()">Home</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Team">Biographies</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Universities">The University(s)</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Future_Directions">Future Directions</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/References">References</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_2">Genetics</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Protocols">Protocols</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements">Acknowledgements</a><br />
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Columbia & Cooper 2012 Team</h2><br />
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The Effects of A. ferrooxidans</h2><br />
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<div style="width:950px; background-color:#5C3317;" class="secheader">The Project</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<div id="ctop" style="background:#238E23;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Genetics</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, ferrooxidans (the bacteria), and other chemicals. Using our liquid media, we were able to grow healthy ferrooxidans and simultaneously dissolve (etch) copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. We have utilized nail polish as a varnish to control the etching until the genetics group completes our biological controled etching mechanism. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
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<a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">here</a> for a full list of our submitted parts.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-03T14:26:16Z
<p>Ymakita: </p>
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<div style="width:950px; background-color:#5C3317;" class="secheader">The Project</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<div id="lefttop" style="background:#B87333; background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png');" class="secheader">iGEM</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<div id="ctop" style="background:#238E23;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Genetics</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, ferrooxidans (the bacteria), and other chemicals. Using our liquid media, we were able to grow healthy ferrooxidans and simultaneously dissolve (etch) copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. We have utilized nail polish as a varnish to control the etching until the genetics group completes our biological controled etching mechanism. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
<br />
<a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">here</a> for a full list of our submitted parts.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-03T14:24:33Z
<p>Ymakita: </p>
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<li><a href="https://2012.igem.org/Team:Columbia-Cooper-NYC" onmouseover="mopen('m1')" onmouseout="mclosetime()">Home</a><br />
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<li><a href="#" onmouseover="mopen('m2')" onmouseout="mclosetime()">Team</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Team">Biographies</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Facilitators">Facilitators</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Universities">The University(s)</a><br />
<a href="https://igem.org/Team.cgi?year=2012">Official Profile</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">Overview</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Data_and_Conclusions">Data and Conclusions</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Future_Directions">Future Directions</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/References">References</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_2">Genetics</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">Copper Etching</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Protocols">Protocols</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">Outreach</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Safety">Safety</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements">Acknowledgements</a><br />
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Columbia & Cooper 2012 Team</h2><br />
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The Effects of A. ferrooxidans</h2><br />
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<div style="width:950px; background-color:#5C3317;" class="secheader">The Project</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<div id="ctop" style="background:#238E23;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Genetics</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, ferrooxidans (the bacteria), and other chemicals. Using our liquid media, we were able to grow healthy ferrooxidans and simultaneously dissolve (etch) copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. We have utilized nail polish as a varnish to control the etching until the genetics group completes our biological controled etching mechanism. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
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<a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">here</a> for a full list of our submitted parts.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-03T14:23:06Z
<p>Ymakita: </p>
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<div style="width:950px; background-color:#5C3317;" class="secheader">The Project</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
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background: -moz-linear-gradient(top, #f2f2f2, #f8f8f8); color:#333333; height:350px;"><br />
<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, ferrooxidans (the bacteria), and other chemicals. Using our liquid media, we were able to grow healthy ferrooxidans and simultaneously dissolve (etch) copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. We have utilized nail polish as a varnish to control the etching until the genetics group completes our biological controled etching mechanism. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
<br />
<a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">here</a> for a full list of our submitted parts.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-03T14:18:50Z
<p>Ymakita: </p>
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<li><a href="https://2012.igem.org/Team:Columbia-Cooper-NYC" onmouseover="mopen('m1')" onmouseout="mclosetime()">Home</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Team">Biographies</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Universities">The University(s)</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">Parts Submitted</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_2">Genetics</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">Copper Etching</a><br />
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<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Sponsor_Us">Sponsor Us</a><br />
<a href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Acknowledgements">Acknowledgements</a><br />
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Columbia & Cooper 2012 Team</h2><br />
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Copper Etching</h2><br />
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The Effects of A. ferrooxidans</h2><br />
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<div style="width:950px; background-color:#5C3317;" class="secheader">The Project</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<div id="ctop" style="background:#238E23;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Genetics</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, ferrooxidans (the bacteria), and other chemicals. Using our liquid media, we were able to grow healthy ferrooxidans and simultaneously dissolve (etch) copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. We have utilized nail polish as a varnish to control the etching until the genetics group completes our biological controled etching mechanism. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
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<a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">here</a> for a full list of our submitted parts.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/Main
Team:Columbia-Cooper-NYC/Main
2012-10-03T14:15:44Z
<p>Ymakita: </p>
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<div style="width:950px; background-color:#5C3317;" class="secheader">The Project</div><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"><br />
The Columbia-Cooper iGEM team is working with Acidithiobacillus ferrooxidans to create a light-controlled printed circuit board manufacturing process. This bacteria’s metabolism relies on its ability to oxidize iron; the iron can then be used to oxidize, and in turn solubilize, copper. By genetically altering the bacteria, we will install a light sensitive mechanism which will enable controlled copper etching, leaving a finished circuit board. Once a blank printed circuit board is placed in a thin layer of solid media, the bacteria will be applied onto the surface of the media and light of the appropriate wavelength will be focused on it in a desired pattern. The light sensitive mechanism in A. ferrooxidans will activate a self-destructing mechanism preventing copper etching in these locations. In the end, the circuit board will be "etched" by the bacteria everywhere that is not illuminated, leaving a desired pattern on the circuit board under the cells in the path of the light. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Overview">here</a> for details. </p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> The <a style="color:#6bbe00 !important" href="https://igem.org/Main_Page">International Genetically Engineered Machine competition (iGEM)</a> is the premiere undergraduate Synthetic Biology competition. Student teams are given a kit of biological parts from the <a style="color:#6bbe00 !important" href="http://partsregistry.org/Main_Page">Registry of Standard Biological Parts</a>. Working at their own schools over the summer, they use these and new parts of their own design to build biological systems and operate them in living cells. This project design and competition format is an exceptionally motivating and effective teaching method.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;">Our Genetics Team was responsible for designing and implementing a series of genes which would allow us to exert light based spatial control of apoptosis in E.coli, and eventually transition into A. ferrooxidans. This design includes the expression of a light sensor, which, when exposed to specific wavelengths of light, triggers transcription of a lysis cassette. A few of the parts which we experimented with are <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K952000">BBa_K952000</a>, <a style="color:#6bbe00 !important" href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K592016">BBa_K592016</a>, and <a style="color:#6bbe00 !important" href="http://partsregistry.org/Part:BBa_K124017">BBa_K124017</a>.<br />
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<div id="rtop" style="background:#B87333;background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png')" class="secheader">Copper Etching</div><br />
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background: -moz-linear-gradient(top, #f2f2f2, #f8f8f8); color:#333333; height:350px;"><br />
<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:77%;"> Our project is to revamp a chemical and mechanical manufacturing process, so in addition to working with DNA, we also worked on macro-scale batches of copper foil, ferrooxidans (the bacteria), and other chemicals. Using our liquid media, we were able to grow healthy ferrooxidans and simultaneously dissolve (etch) copper foil much faster than the basal rate (i.e. copper in the liquid media without ferrooxidans). Since our PCB manufacturing process requires the ferrooxidans to "stay put", we have been developing a solid agar-based media, on which the ferrooxidans grow, and below which the copper is etched, again faster than the basal rate. We have utilized nail polish as a varnish to control the etching until the genetics group completes our biological controled etching mechanism. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Columbia_notebook_1">here</a> for details</a>.<br />
</a><br />
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</div><br />
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<div id="lefttop" style="background:#238E23; background-image:url('https://static.igem.org/mediawiki/2010/a/ad/Cam-Gradient-Overlay.png');" class="secheader">Biobrick</div><br />
<div id="leftcontent" style="background:-webkit-gradient(linear, left top, left bottom, from(#f2f2f2), to(#f8f8f8)); <br />
background: -moz-linear-gradient(top, #f2f2f2, #f8f8f8); color:#333333; height:250px;"><br />
<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team submitted multiple composite parts, which were built from preexisting Biobricks and used in our project. We also submitted a novel red light sensing protein domain, FphA753s, which was constructed to conform to the RFC25 – Freiburg fusion standard, and is intended for future use to allow light based control of transcription. Click<br />
<br />
<a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Parts_Submitted">here</a> for a full list of our submitted parts.</p><br />
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<p style="line-height:140%; padding-left:10px; padding-top:10px; padding-right:10px;text-align:justify; font-size:90%;"> Our team organized a booth at the 2012 Maker Faire in New York City to share the work we've been doing with the public. We also made 3 interactive games to teach children about recombinant DNA and the various forms of bacterial transformation. Click <a style="color:#6bbe00 !important" href="https://2012.igem.org/Team:Columbia-Cooper-NYC/Outreach">here</a> for details.</a>.<br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial
Team:Columbia-Cooper-NYC/trial
2012-10-03T14:12:36Z
<p>Ymakita: </p>
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Columbia & Cooper 2012 Team</h2><br />
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The Effects of A. ferrooxidans</h2><br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial
Team:Columbia-Cooper-NYC/trial
2012-10-03T14:11:05Z
<p>Ymakita: </p>
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</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8316/8049640302_5ae1a9a049_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
Maker Faire (Copyright © Andrew Cribb)</h2><br />
</div><br />
</li><br />
</ul><br />
</div><br />
<div class="lof-navigator-wapper"><br />
<div class="lof-navigator-outer"><br />
<br />
<br />
<ul class="lof-navigator"><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8181/8049658043_cffa2b28e0_t.jpg"><br />
</li><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8030/8049658065_76d444054c_t.jpg"><br />
</li><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8313/8049658081_5522c4a121_t.jpg"><br />
</li><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8041/8049663090_89a1de0f3c_t.jpg"><br />
</li><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8035/8049658117_e74a561066_t.jpg"><br />
</li><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8034/8049663114_8d3b7152a9_t.jpg"><br />
</li><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8461/8049658157_20b02010b7_t.jpg"><br />
</li><br />
</ul><br />
<br />
<br />
</div><br />
</div><br />
</div><br />
<br />
<br />
<br />
<div id="hokkaidou-right-content"><br />
</div><br />
<br />
<br />
</div><br />
</div><br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<script type="text/javascript"><br />
$(document).ready(function () {<br />
<br />
<br />
jQuery.cookie = function (d, f, b) { function e(j, i) { if (j) { if (i) { return true } } return false } if (e(arguments.length > 1, String(f) !== "[object Object]")) { b = jQuery.extend({}, b); if (f === null || f === undefined) { b.expires = -1 } if (typeof b.expires === "number") { var h = b.expires, c = b.expires = new Date(); c.setDate(c.getDate() + h) } f = String(f); return (document.cookie = [encodeURIComponent(d), "=", b.raw ? f : encodeURIComponent(f), b.expires ? "; expires=" + b.expires.toUTCString() : "", b.path ? "; path=" + b.path : "", b.domain ? "; domain=" + b.domain : "", b.secure ? "; secure" : ""].join("")) } b = f || {}; var a, g = b.raw ? function (i) { return i } : decodeURIComponent; return (a = new RegExp("(?:^|; )" + encodeURIComponent(d) + "=([^;]*)").exec(document.cookie)) ? g(a[1]) : null };<br />
<br />
<br />
$('.right-menu, .left-menu').fadeTo(0, 0);<br />
$('.right-menu, .left-menu').bind('mouseover', function () {<br />
$(this).fadeTo('slow', 1);<br />
});<br />
<br />
<br />
$(function () {<br />
$('img').each(function () {<br />
var thumb = $(this).attr('src');<br />
var reg = new RegExp('^(\/wiki\/images)\/thumb');<br />
if (thumb.match(reg)) {<br />
var image = thumb.replace(reg, '$1');<br />
image = image.replace(/[^\/]+?$/, '').replace(/\/$/, '');<br />
var $tag = $('<img>').attr('src', image);<br />
$(this).closest('a').bind('click', function () {<br />
$('<div>').append($tag).lightbox_me();<br />
return false;<br />
});<br />
}<br />
});<br />
});<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
var buttons = {<br />
previous: $('#lofslidercontent45 .lof-previous'),<br />
next: $('#lofslidercontent45 .lof-next')<br />
};<br />
$obj = $('#lofslidecontent45').lofJSidernews({<br />
interval: 5000,<br />
direction: 'opacitys',<br />
easing: 'easeInOutExpo',<br />
duration: 1200,<br />
auto: true,<br />
maxItemDisplay: 7,<br />
startItem: 0,<br />
navPosition: 'horizontal', // horizontal<br />
navigatorHeight: 32,<br />
navigatorWidth: 80,<br />
mainWidth: 780,<br />
buttons: buttons<br />
});<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
});<br />
</script><br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
</body><br />
</html></div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial
Team:Columbia-Cooper-NYC/trial
2012-10-03T14:09:52Z
<p>Ymakita: </p>
<hr />
<div><html><br />
<body><br />
<script type="text/javascript" src="https://static.igem.org/mediawiki/2011/1/1b/IGEM_HokkaidoU_JS_Slideshow.txt"></script><br />
<br />
<link rel="Stylesheet" href="https://static.igem.org/mediawiki/2012/2/29/Igem_slider_styles.txt" /><br />
<br />
<div id="hokkaidou-container"><br />
<div id="hokkaidou-content"><br />
<br />
<div id="lofslidecontent45" class="lof-slidecontent"><br />
<div style="display: none;" class="preload"><br />
<div><br />
</div><br />
</div><br />
<div class="lof-main-outer"><br />
<ul class="lof-main-wapper"><br />
<li><br />
<img src="http://farm9.staticflickr.com/8456/8049457082_5814030096_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
Columbia & Cooper 2012 Team</h2><br />
</div><br />
</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8038/8049568856_b4d1d26031_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
Columbia University</h2><br />
</div><br />
</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8312/8049592851_58d8d91127_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
The Cooper Union for the Advancement of Science and Art</h2><br />
</div><br />
</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8173/8049607828_34eedef20f_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
Genetics</h2><br />
</div><br />
</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8039/8049606505_8dedbcd5c7_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
Copper Etching</h2><br />
</div><br />
</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8176/8049610201_05aecf6db9_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
The Effects of A. ferrooxidans</h2><br />
</div><br />
</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8316/8049640302_5ae1a9a049_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
Maker Faire (Copyright © Andrew Cribb)</h2><br />
</div><br />
</li><br />
</ul><br />
</div><br />
<div class="lof-navigator-wapper"><br />
<div class="lof-navigator-outer"><br />
<br />
<br />
<ul class="lof-navigator"><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8181/8049658043_cffa2b28e0_t.jpg"><br />
</li><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8030/8049658065_76d444054c_t.jpg"><br />
</li><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8313/8049658081_5522c4a121_t.jpg"><br />
</li><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8041/8049663090_89a1de0f3c_t.jpg"><br />
</li><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8035/8049658117_e74a561066_t.jpg"><br />
</li><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8034/8049663114_8d3b7152a9_t.jpg"><br />
</li><br />
<li class="" style="height: 32px; width: 80px;"><br />
<img src="http://farm9.staticflickr.com/8461/8049658157_20b02010b7_t.jpg"><br />
</li><br />
</ul><br />
<br />
<br />
</div><br />
</div><br />
</div><br />
<br />
<br />
<br />
<div id="hokkaidou-right-content"><br />
</div><br />
<br />
<br />
</div><br />
</div><br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
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<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<script type="text/javascript"><br />
$(document).ready(function () {<br />
<br />
<br />
jQuery.cookie = function (d, f, b) { function e(j, i) { if (j) { if (i) { return true } } return false } if (e(arguments.length > 1, String(f) !== "[object Object]")) { b = jQuery.extend({}, b); if (f === null || f === undefined) { b.expires = -1 } if (typeof b.expires === "number") { var h = b.expires, c = b.expires = new Date(); c.setDate(c.getDate() + h) } f = String(f); return (document.cookie = [encodeURIComponent(d), "=", b.raw ? f : encodeURIComponent(f), b.expires ? "; expires=" + b.expires.toUTCString() : "", b.path ? "; path=" + b.path : "", b.domain ? "; domain=" + b.domain : "", b.secure ? "; secure" : ""].join("")) } b = f || {}; var a, g = b.raw ? function (i) { return i } : decodeURIComponent; return (a = new RegExp("(?:^|; )" + encodeURIComponent(d) + "=([^;]*)").exec(document.cookie)) ? g(a[1]) : null };<br />
<br />
<br />
$('.right-menu, .left-menu').fadeTo(0, 0);<br />
$('.right-menu, .left-menu').bind('mouseover', function () {<br />
$(this).fadeTo('slow', 1);<br />
});<br />
<br />
<br />
$(function () {<br />
$('img').each(function () {<br />
var thumb = $(this).attr('src');<br />
var reg = new RegExp('^(\/wiki\/images)\/thumb');<br />
if (thumb.match(reg)) {<br />
var image = thumb.replace(reg, '$1');<br />
image = image.replace(/[^\/]+?$/, '').replace(/\/$/, '');<br />
var $tag = $('<img>').attr('src', image);<br />
$(this).closest('a').bind('click', function () {<br />
$('<div>').append($tag).lightbox_me();<br />
return false;<br />
});<br />
}<br />
});<br />
});<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
var buttons = {<br />
previous: $('#lofslidercontent45 .lof-previous'),<br />
next: $('#lofslidercontent45 .lof-next')<br />
};<br />
$obj = $('#lofslidecontent45').lofJSidernews({<br />
interval: 5000,<br />
direction: 'opacitys',<br />
easing: 'easeInOutExpo',<br />
duration: 1200,<br />
auto: true,<br />
maxItemDisplay: 7,<br />
startItem: 0,<br />
navPosition: 'horizontal', // horizontal<br />
navigatorHeight: 32,<br />
navigatorWidth: 80,<br />
mainWidth: 780,<br />
buttons: buttons<br />
});<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
});<br />
</script><br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
</body><br />
</html></div>
Ymakita
http://2012.igem.org/File:Igem_slider_styles.txt
File:Igem slider styles.txt
2012-10-03T14:07:45Z
<p>Ymakita: these are CSS styles for the igem homepage image slider</p>
<hr />
<div>these are CSS styles for the igem homepage image slider</div>
Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial
Team:Columbia-Cooper-NYC/trial
2012-10-03T14:00:34Z
<p>Ymakita: </p>
<hr />
<div><html><br />
<body><br />
<script type="text/javascript" src="https://static.igem.org/mediawiki/2011/1/1b/IGEM_HokkaidoU_JS_Slideshow.txt"></script><br />
<br />
<br />
<style type="text/css"><br />
<br />
<br />
/* <br />
@charset "utf-8";<br />
<br />
<br />
CSS Document */<br />
<br />
.lof-slidecontent, .lof-slidecontent a {<br />
color:#FFF; <br />
}<br />
.lof-slidecontent a.readmore{<br />
color:#58B1EA;<br />
font-size:95%;<br />
<br />
}<br />
.lof-slidecontent{<br />
position:relative;<br />
overflow:hidden;<br />
border:#F4F4F4 solid 1px;<br />
margin: 0 auto 30px auto;<br />
border-radius: 4px;<br />
}<br />
.lof-slidecontent .preload{<br />
height:100%;<br />
width:100%;<br />
position:absolute;<br />
top:0;<br />
left:0;<br />
z-index:100000;<br />
text-align:center;<br />
background:#FFF<br />
}<br />
.lof-slidecontent .preload div{<br />
height:100%;<br />
width:100%;<br />
background:transparent url(https://static.igem.org/mediawiki/2011/5/5d/IGEM_HokkaidoU_Index_Slideshow_Load-indicator.gif) no-repeat scroll 50% 50%;<br />
}<br />
.lof-main-outer{<br />
position:relative;<br />
height:340px;<br />
width:760px;<br />
z-index:3px;<br />
overflow:hidden;<br />
}<br />
<br />
<br />
/*******************************************************/<br />
.lof-main-item-desc{<br />
z-index:100px;<br />
position:absolute;<br />
top:0;<br />
left:0px;<br />
background:url(https://static.igem.org/mediawiki/2011/e/eb/IGEM_HokkaidoU_Index_Slideshow_Bg_trans.png);<br />
/*height:20px;*/<br />
width:100%;<br />
/* filter:0.7(opacity:60) */<br />
padding:12px;<br />
overflow: hidden;<br />
}<br />
.lof-main-item-desc p{<br />
margin:0 8px;<br />
padding:0 0;<br />
font-size: small;<br />
line-height: 1.2em;<br />
}<br />
.lof-main-item-desc h3{<br />
padding:0;<br />
margin:0;<br />
color: #fff;<br />
font-size: small;<br />
border-left: none;<br />
}<br />
.lof-main-item-desc h2{<br />
padding:0;<br />
margin:0;<br />
color: #fff;<br />
border-bottom: none;<br />
font-weight:bold;<br />
}<br />
.lof-main-item-desc h3 a{ <br />
margin:0;<br />
background:#C01F25;<br />
font-size:75%;<br />
padding:2px 3px;<br />
font-family:"Trebuchet MS",Trebuchet,Arial,Verdana,sans-serif;<br />
text-transform:uppercase;<br />
text-decoration:none<br />
}<br />
.lof-main-item-desc h3 a:hover{<br />
<br />
text-decoration:underline;<br />
}<br />
.lof-main-item-desc h3 i {<br />
font-size:70%;<br />
}<br />
<br />
/* main flash */<br />
ul.lof-main-wapper{<br />
/* margin-right:auto; */<br />
overflow:hidden;<br />
background:transparent url(https://static.igem.org/mediawiki/2011/5/5d/IGEM_HokkaidoU_Index_Slideshow_Load-indicator.gif) no-repeat scroll 50% 50%;<br />
padding:0px;<br />
margin:0;<br />
position:absolute;<br />
overflow:hidden;<br />
}<br />
<br />
ul.lof-main-wapper li{<br />
overflow:hidden;<br />
padding:0px;<br />
margin:0px;<br />
float:left;<br />
position:relative;<br />
}<br />
.lof-opacity li{<br />
position:absolute;<br />
top:0;<br />
left:0;<br />
float:inherit;<br />
}<br />
ul.lof-main-wapper li img{<br />
padding:0px; <br />
}<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
/* item navigator */<br />
.lof-navigator-wapper {<br />
position:absolute;<br />
bottom:10px;<br />
left:10px;<br />
width:740px;<br />
height:40px;<br />
background:url(https://static.igem.org/mediawiki/2011/b/b8/IGEM_HokkaidoU_Index_Slideshow_Transparent_bg.png) repeat;<br />
padding:5px 0 0 5px;<br />
}<br />
.lof-navigator-outer{<br />
position:relative;<br />
z-index:100;<br />
/*height:60px;<br />
width:780px;*/<br />
overflow:hidden;<br />
color:#FFF;<br />
/*float:left */<br />
}<br />
ul.lof-navigator{<br />
top:0;<br />
padding:0;<br />
margin:0;<br />
/*position:absolute;<br />
width:600px;*/<br />
}<br />
ul.lof-navigator li{<br />
cursor:hand; <br />
cursor:pointer;<br />
list-style:none;<br />
padding:0;<br />
margin-left:0px;<br />
overflow:hidden;<br />
float:left;<br />
display:block;<br />
<br />
text-align:center;<br />
<br />
}<br />
ul.lof-navigator li img{<br />
border:#666 solid 3px; <br />
}<br />
ul.lof-navigator li.active img, ul.lof-navigator li:hover img {<br />
border:#A8A8A8 solid 3px;<br />
}<br />
.lof-navigator-wapper .lof-next, .lof-navigator-wapper .lof-previous{<br />
display:block;<br />
width:22px;<br />
height:30px;<br />
color:#FFF;<br />
cursor:pointer;<br />
<br />
}<br />
.lof-navigator-wapper .lof-next {<br />
float:left; <br />
text-indent:-999px;<br />
margin-right:5px;<br />
background:url(https://static.igem.org/mediawiki/2011/9/9c/IGEM_HokkaidoU_Index_Slideshow_Arrow-l.png) no-repeat right center;<br />
}<br />
.lof-navigator-wapper .lof-previous {<br />
float:left; <br />
text-indent:-999px;<br />
margin-left:5px;<br />
background:url(https://static.igem.org/mediawiki/2011/9/98/IGEM_HokkaidoU_Index_Slideshow_Arrow-r.png) no-repeat left center;<br />
}<br />
<br />
<br />
<br />
#hokkaidou-container{<br />
width: 780px;<br />
margin: 0 auto;<br />
padding: 0;<br />
}<br />
<br />
#hokkaidou-content<br />
{<br />
zoom: 1;<br />
}<br />
#hokkaidou-content:after<br />
{<br />
content: "";<br />
}<br />
#hokkaidou-content #hokkaidou-right-content<br />
{<br />
/*float: right;<br />
width: 680px; */<br />
}<br />
</style><br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<br />
<div id="hokkaidou-container"><br />
<div id="hokkaidou-content"><br />
<br />
<div id="lofslidecontent45" class="lof-slidecontent"><br />
<div style="display: none;" class="preload"><br />
<div><br />
</div><br />
</div><br />
<div class="lof-main-outer"><br />
<ul class="lof-main-wapper"><br />
<li><br />
<img src="http://farm9.staticflickr.com/8456/8049457082_5814030096_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
Columbia & Cooper 2012 Team</h2><br />
</div><br />
</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8038/8049568856_b4d1d26031_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
Columbia University</h2><br />
</div><br />
</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8312/8049592851_58d8d91127_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
The Cooper Union for the Advancement of Science and Art</h2><br />
</div><br />
</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8173/8049607828_34eedef20f_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
Genetics</h2><br />
</div><br />
</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8039/8049606505_8dedbcd5c7_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
Copper Etching</h2><br />
</div><br />
</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8176/8049610201_05aecf6db9_b.jpg"><br />
<div class="lof-main-item-desc"><br />
<h2><br />
The Effects of A. ferrooxidans</h2><br />
</div><br />
</li><br />
<li><br />
<img src="http://farm9.staticflickr.com/8316/8049640302_5ae1a9a049_b.jpg"><br />
<div class="lof-main-item-desc"><br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial9
Team:Columbia-Cooper-NYC/trial9
2012-10-03T13:58:06Z
<p>Ymakita: </p>
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Columbia & Cooper 2012 Team</h2><br />
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The Cooper Union for the Advancement of Science and Art</h2><br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial
Team:Columbia-Cooper-NYC/trial
2012-10-03T13:57:49Z
<p>Ymakita: </p>
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Columbia & Cooper 2012 Team</h2><br />
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The Cooper Union for the Advancement of Science and Art</h2><br />
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Genetics</h2><br />
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Copper Etching</h2><br />
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The Effects of A. ferrooxidans</h2><br />
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Maker Faire (Copyright © Andrew Cribb)</h2><br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial9
Team:Columbia-Cooper-NYC/trial9
2012-10-03T13:57:36Z
<p>Ymakita: </p>
<hr />
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Genetics</h2><br />
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Copper Etching</h2><br />
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The Effects of A. ferrooxidans</h2><br />
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Maker Faire (Copyright © Andrew Cribb)</h2><br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial
Team:Columbia-Cooper-NYC/trial
2012-10-03T13:54:07Z
<p>Ymakita: </p>
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial
Team:Columbia-Cooper-NYC/trial
2012-10-03T13:53:16Z
<p>Ymakita: </p>
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial
Team:Columbia-Cooper-NYC/trial
2012-10-03T13:51:51Z
<p>Ymakita: </p>
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial
Team:Columbia-Cooper-NYC/trial
2012-10-03T13:51:06Z
<p>Ymakita: </p>
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The Effects of A. ferrooxidans</h2><br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial
Team:Columbia-Cooper-NYC/trial
2012-10-03T13:49:45Z
<p>Ymakita: </p>
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Columbia & Cooper 2012 Team</h2><br />
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Genetics</h2><br />
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Copper Etching</h2><br />
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The Effects of A. ferrooxidans</h2><br />
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Maker Faire (Copyright © Andrew Cribb)</h2><br />
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Ymakita
http://2012.igem.org/Team:Columbia-Cooper-NYC/trial
Team:Columbia-Cooper-NYC/trial
2012-10-03T13:48:39Z
<p>Ymakita: </p>
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