Team:Queens Canada/Notebook/Week4

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<h1> Monday May 28  </h1> <p> <h2>Throughout the day, we mostly worked again on sponsorship, but we also got some time in the lab and we performed the plasmid dehydration and growing colonies on plates for three different biobrick parts. Essentially the next few days in the lab is going to consist of isolating plasmids from different biobrick parts. The parts we incubated today are BBa_K190019 (fmT), BBa_K346003 (RBS(B0032)+MBP) and BBa_K346001 (MerR). On the wiki side of things, Phillip edited the wiki so that the notebook section is nearly ready to go up! </h2> </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 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> Tuesday May 29</h1> <h2> <p> In the morning, we used
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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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<h1> Wednesday May 30</h1>
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<h1> Thursday May 31</h1>
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<h1> Friday June 1</h1>
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<script>
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Revision as of 14:22, 31 May 2012

Control

Notebook - Week 3

Protocol Content

Monday May 21

Today was Victoria day, a statutory holiday in Canada, so we took the day 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 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.

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 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.

Thursday May 24

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.

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 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.