Team:University College London/Notebook/Week3

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<div class="notebook-training">  '''Training – Wet lab'''Training - Today four of us (James Rutley, Bethan Wolfenden, Bouran Sohrabi, Philipp Boeing) had a training on how to make competent cells which was organized by one of our iGEM advisers - Alex. We completed one out of three training stages which was making minimal media and plating out our e.coli. This will lead onto the second stage (tomorrow) which is inoculation of colonies.</div>  
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<div class="notebook-training">  '''Training – Wet lab''' Today four of us (James Rutley, Bethan Wolfenden, Bouran Sohrabi, Philipp Boeing) had a training on how to make competent cells which was organized by one of our iGEM advisers - Alex. We completed one out of three training stages which was making minimal media and plating out our e.coli. This will lead onto the second stage (tomorrow) which is inoculation of colonies.</div>  
<div class="notebook-meeting"> '''Meeting – Construction/Characterisation''' Today we had construction/characterization meeting with our main supervisor Darren Nesbeth. The outcome of the meeting was finalization of five modules which now are aggregation, salt tolerance, degradation, buoyancy, containment (receptor module was included into aggregation module). Tac promoter was chosen for degradation and salt tolerance modules in case any toxicity is present.
<div class="notebook-meeting"> '''Meeting – Construction/Characterisation''' Today we had construction/characterization meeting with our main supervisor Darren Nesbeth. The outcome of the meeting was finalization of five modules which now are aggregation, salt tolerance, degradation, buoyancy, containment (receptor module was included into aggregation module). Tac promoter was chosen for degradation and salt tolerance modules in case any toxicity is present.
This meeting made our wet lab plan more solid this will allow us to start working on our first module (aggregation) the following week.</div>
This meeting made our wet lab plan more solid this will allow us to start working on our first module (aggregation) the following week.</div>

Revision as of 11:32, 26 June 2012

Notebook: Week 3

Preparations | Week 1 | Week 2 | Week 3 | Week 4 | Week 5 | Week 6 | Week 7 | Week 8 | Week 9 | Week 10 | Week 11 | Week 12 | Week 13 | Week 14 | Week 15 | Week 16

Aims For This Week

This week we will be presenting our progress in all aspects of the project to our supervisors, but our key aim is to demonstrate that we have progressed sufficiently to begin construction.


Training – Wet lab Today four of us (James Rutley, Bethan Wolfenden, Bouran Sohrabi, Philipp Boeing) had a training on how to make competent cells which was organized by one of our iGEM advisers - Alex. We completed one out of three training stages which was making minimal media and plating out our e.coli. This will lead onto the second stage (tomorrow) which is inoculation of colonies.
Meeting – Construction/Characterisation Today we had construction/characterization meeting with our main supervisor Darren Nesbeth. The outcome of the meeting was finalization of five modules which now are aggregation, salt tolerance, degradation, buoyancy, containment (receptor module was included into aggregation module). Tac promoter was chosen for degradation and salt tolerance modules in case any toxicity is present. This meeting made our wet lab plan more solid this will allow us to start working on our first module (aggregation) the following week.