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Team:Queens Canada/Notebook/Week3
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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> | <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> | ||
| - | <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 </p> </div> | + | <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 currently 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, we can move 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. Performed the miniprep procedure on the liquid colonies. Involves adding a lot of different solutions as well as centrifuging. 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 fluores. After work, Kevin and the rest of the team involved in SynthetiQ brainstormed some ideas for some videos. </p> </h2></div> |
Revision as of 17:59, 30 May 2012
Notebook - Week 3
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 currently 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, we can move on to miniprep (isolating the plasmid from the colonies). We spent our time in the lab today preparing for the miniprep procedure tomorrow.
