Team:UCL London/Week 10

From 2010.igem.org

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=Crucial Deadlines week - Week 10=
=Crucial Deadlines week - Week 10=
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==Monday 30th August==
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Today was a very decisive day indeed, we had to overcome several obstacles, one being the possibility of losing one of our main sponsorship bids. But nevertheless, we had to do some urgent reshuffling of tasks and have now unleashed a new wave of sponsorship haggling,... biopharmaceutical companies, be prepared!!!
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This week was a very decisive week indeed, we had to overcome several obstacles, one being the possibility of losing one of our main sponsorship bids. But nevertheless, we had to do some urgent reshuffling of tasks and have now unleashed a new wave of sponsorship haggling,... biopharmaceutical companies, be prepared!!!
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==Tuesday 31st August==
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Day 1 without the biochemists! Alas the time has come for us biochemical engineers to take over the lab work due to the departure of our biochemists. It just happened that there was also a tube strike this same day, but no, this was not going to stop us! Plan was to start lab work at 10 am, nevertheless, we got into uni about 4pm, but you know what they say, better late then never. We had to carry out a transformation...no comment.
Day 1 without the biochemists! Alas the time has come for us biochemical engineers to take over the lab work due to the departure of our biochemists. It just happened that there was also a tube strike this same day, but no, this was not going to stop us! Plan was to start lab work at 10 am, nevertheless, we got into uni about 4pm, but you know what they say, better late then never. We had to carry out a transformation...no comment.
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But on a serious note, our plan for the week was to successfully transform the RBS-pTAC part into component cells. We carried out the usual transformation protocol where we streaked the part onto nutrient agar plates and then left overnight. But the following day there was no growth at all, not even on the positive control. And so we measured the concentration of the part use..... . We concluded that even though the concentration was in the region of 5g/L, that was sufficient to carry on with the transformation. The part was meant to be in a Kanamysin backbone so it made us wonder maybe that was not the case and it may have been placed in another backbone by the biochemists. We then decided to repeat the experiment this time using multiple plates, 1xAmphiciin, 1xKanamycin, 1xChlorophenical. This time, we sucessfully transformed the parts in the Kanamycin agar plate. These parts were essential as we planned on fermenting them the week after.
   
   
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In terms of modelling, Elena was cracking away at that, she set up meetings with several senior lecturers and pHD students to help with the various aspects of our circuit that needed modelling. Plans were being made to attempt to model the economic aspects behind our project.
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==Wednesday 1st September==
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Elena made an attempt to update the wiki...but without Omar's help that didn't really work out! A few more photos were added, a few more comments were made. Everyone in the team, on their own way, are working on it. Some wet lab, some modeling, some efforts to approach sponsors.
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==Thursday 2nd September==
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it was quite an insight.
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==Friday 3rd September==
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==Saturday==
 
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==Sunday==
 
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Revision as of 09:48, 21 October 2010

UCL IGEM 2010

RETURN TO IGEM 2010

Crucial Deadlines week - Week 10

UCL-Dave.JPG
UCL-lab1.JPG

This week was a very decisive week indeed, we had to overcome several obstacles, one being the possibility of losing one of our main sponsorship bids. But nevertheless, we had to do some urgent reshuffling of tasks and have now unleashed a new wave of sponsorship haggling,... biopharmaceutical companies, be prepared!!!

Day 1 without the biochemists! Alas the time has come for us biochemical engineers to take over the lab work due to the departure of our biochemists. It just happened that there was also a tube strike this same day, but no, this was not going to stop us! Plan was to start lab work at 10 am, nevertheless, we got into uni about 4pm, but you know what they say, better late then never. We had to carry out a transformation...no comment.

But on a serious note, our plan for the week was to successfully transform the RBS-pTAC part into component cells. We carried out the usual transformation protocol where we streaked the part onto nutrient agar plates and then left overnight. But the following day there was no growth at all, not even on the positive control. And so we measured the concentration of the part use..... . We concluded that even though the concentration was in the region of 5g/L, that was sufficient to carry on with the transformation. The part was meant to be in a Kanamysin backbone so it made us wonder maybe that was not the case and it may have been placed in another backbone by the biochemists. We then decided to repeat the experiment this time using multiple plates, 1xAmphiciin, 1xKanamycin, 1xChlorophenical. This time, we sucessfully transformed the parts in the Kanamycin agar plate. These parts were essential as we planned on fermenting them the week after.


In terms of modelling, Elena was cracking away at that, she set up meetings with several senior lecturers and pHD students to help with the various aspects of our circuit that needed modelling. Plans were being made to attempt to model the economic aspects behind our project.



 

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