Team:Queens Canada/Notebook/Week4

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<p>Notebook - Week 4</p>
<p>Notebook - Week 4</p>
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Week
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week1">1</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week2">2</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week3">3</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week4">4</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week5">5</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week6">6</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week7">7</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week8">8</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week9">9</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week10">10</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week11">11</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week12">12</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week13">13</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week14">14</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week15">15</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week16">16</a> </li>
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<li> <a href="https://2012.igem.org/Team:Queens_Canada/Notebook/Week17">17+</a> </li>
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<tr class="tableizer-firstrow"><th>Date</th><th>Protocol</th><th>People</th><th>DNA (if relevant)</th><th>Quantities and Parameters (if relevant)</th></tr> <tr><td>May-22</td><td>Heat Shock Transformation</td><td>Kevin and Friends</td><td>BBa_J04450 - RFP</td><td>&nbsp;</td></tr> <tr><td>&nbsp;</td><td>Prepared Antibiotic plates</td><td>Kevin and Friends</td><td>&nbsp;</td><td>Added 25 uL of chloramphenicol </td></tr> <tr><td>May-23</td><td>Heat Shock Transformation</td><td>Victor, Aaron, Hope, David Faisal</td><td>BBa_J04450 - RFP</td><td>&nbsp;</td></tr> <tr><td>May-24</td><td>Liquid Cultures</td><td>Victor, Kevin, Faisal, Maggie</td><td>BBa_J04450 - RFP</td><td>Added 160 mL of absolute ethanol into Solution 1 </td></tr> <tr><td>May-25</td><td>Miniprep</td><td>Victor, Kevin, Faisal, David, Phillip</td><td>RFP</td><td>Four trials were minipreped</td></tr></table>
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         <h1> Monday May 21</h1>  <p> <h2> Today was Victoria day, a statutory holiday in Canada, so we took the day to rest and relax and prepare for the week ahead!</p> </h2> <h1>Tuesday May 22</h1> <h2> <p> First day in lab hurray! </p>
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         <h1> Monday May 21</h1>  <p> <h2> Today was Victoria Day, a statutory holiday in Canada, so we took the day off to rest and relax and prepare for the week ahead!</p> </h2> <h1>Tuesday May 22</h1> <h2> <p> First day in lab hurray! </p>
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<p>In the morning we went over lab training/ safety orientation, as well as completing WHMIS training, that must have been completed before we enter the lab. In the afternoon we cleaned up our assigned lab bench in preparation for our work in the lab tomorrow.</p>  <h1> Wednesday May 23 </h1> <h2> <p> This morning we worked mainly on primer design in preparation for PCR work. Kevin also met with one of our advisors, Dr. Allingham in order to discussing modeling the protein design. In the afternoon, we tested different protocols on transformation of Red Fluorescent Protein (RFP) DNA biobricks into LB plates with chloramphenicol anitibiotic resistance. Four trials were incubated at 37 degrees celcius overnight. </h2> </p> <h1> Thursday May 24 </h1> <h2> <p> We spend the majority of the day working on sponsorship, following up on emails sent. We also spent some time in the lab. We got red colonies in the liquid medium shown as a cloudy red liquid, and we moved on to miniprep (isolating the plasmid from the colonies). We spent our time in the lab today preparing for the miniprep procedure tomorrow. </h2> </p> <h1> Friday May 25 </h1> <h2> Today we worked more on sponsorship in the morning, and got into the lab in the afternoon. We performed the miniprep procedure on the liquid colonies which involved adding a lot of different solutions as well as centrifugation. We isolated BBa_J04450, and stored it in the fridge at -20 degrees celcius.  We also looked at the red colonies under the microscope and they did fluoresce. After work, Kevin and the rest of the team involved in SynthetiQ brainstormed some ideas for some videos. </p> </h2>
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<p>In the morning we went over lab training/safety orientation, as well as completed WHMIS training necessary to work in the lab. In the afternoon we cleaned up our assigned lab bench in preparation for our work in the lab tomorrow.</p>  <h1> Wednesday May 23 </h1> <h2> <p> This morning we worked mainly on primer design in preparation for PCR work. Kevin also met with one of our advisors, Dr. Allingham, in order to discuss modelling protein designs. In the afternoon, we tested different protocols on transformation of the Red Fluorescent Protein (RFP) BioBrick into LB plates with chloramphenicol resistance. Four trials were incubated at 37 degrees Celsius overnight. </h2> </p> <h1> Thursday May 24 </h1> <h2> <p> We spent the majority of the day working on sponsorship, following up on emails sent. We also spent some time in the lab. We got red colonies in the liquid medium shown as a cloudy red liquid, and we moved on to miniprep (isolating the plasmid from the colonies). We spent our time in the lab today preparing for the miniprep procedure tomorrow. </h2> </p> <h1> Friday May 25 </h1> <h2> Today we worked more on sponsorship in the morning, and got into the lab in the afternoon. We performed the miniprep procedure on the liquid colonies, which involved adding a lot of different solutions as well as centrifugation. We isolated BBa_J04450, and stored it in the fridge at -20 degrees Celsius.  We also looked at the red colonies under the microscope, and they did fluoresce. After work, Kevin and the rest of the team involved in SynthetiQ brainstormed some ideas for videos. </p> </h2>
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Latest revision as of 03:50, 4 October 2012
Control

Notebook - Week 4

DateProtocolPeopleDNA (if relevant)Quantities and Parameters (if relevant)
May-22Heat Shock TransformationKevin and FriendsBBa_J04450 - RFP 
 Prepared Antibiotic platesKevin and Friends Added 25 uL of chloramphenicol
May-23Heat Shock TransformationVictor, Aaron, Hope, David FaisalBBa_J04450 - RFP 
May-24Liquid CulturesVictor, Kevin, Faisal, MaggieBBa_J04450 - RFPAdded 160 mL of absolute ethanol into Solution 1
May-25MiniprepVictor, Kevin, Faisal, David, PhillipRFPFour trials were minipreped

Monday May 21

Today was Victoria Day, a statutory holiday in Canada, so we took the day off to rest and relax and prepare for the week ahead!

Tuesday May 22

First day in lab hurray!

In the morning we went over lab training/safety orientation, as well as completed WHMIS training necessary to work in the lab. In the afternoon we cleaned up our assigned lab bench in preparation for our work in the lab tomorrow.

Wednesday May 23

This morning we worked mainly on primer design in preparation for PCR work. Kevin also met with one of our advisors, Dr. Allingham, in order to discuss modelling protein designs. In the afternoon, we tested different protocols on transformation of the Red Fluorescent Protein (RFP) BioBrick into LB plates with chloramphenicol resistance. Four trials were incubated at 37 degrees Celsius overnight.

Thursday May 24

We spent the majority of the day working on sponsorship, following up on emails sent. We also spent some time in the lab. We got red colonies in the liquid medium shown as a cloudy red liquid, and we moved on to miniprep (isolating the plasmid from the colonies). We spent our time in the lab today preparing for the miniprep procedure tomorrow.

Friday May 25

Today we worked more on sponsorship in the morning, and got into the lab in the afternoon. We performed the miniprep procedure on the liquid colonies, which involved adding a lot of different solutions as well as centrifugation. We isolated BBa_J04450, and stored it in the fridge at -20 degrees Celsius. We also looked at the red colonies under the microscope, and they did fluoresce. After work, Kevin and the rest of the team involved in SynthetiQ brainstormed some ideas for videos.

Retrieved from "http://2012.igem.org/Team:Queens_Canada/Notebook/Week4"