Team:TUDelft/24 July 2009
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===Daniel=== | ===Daniel=== | ||
Since the top10 competent cells newly prepared by us using the Openwetware protocol, didn't transform well for Tim Weenink we are in a bit crisis for competent cells. Anyway to make sure whether the cells work or not I did transformation of Biobricks RBS[B0034] and pLacI[R0010] in the newly created top10 competent cells and kept in drawer to grow in the weekend. | Since the top10 competent cells newly prepared by us using the Openwetware protocol, didn't transform well for Tim Weenink we are in a bit crisis for competent cells. Anyway to make sure whether the cells work or not I did transformation of Biobricks RBS[B0034] and pLacI[R0010] in the newly created top10 competent cells and kept in drawer to grow in the weekend. | ||
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+ | ===Orr=== | ||
+ | Today, I performed the mfold analysis to find out the secondary structures of the key3c and the lock3c. I also started looking at the COSMIC code that is intended to model conjugation. So far I only downloaded the source codes, and still need to find out how to run it. | ||
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{{Template:TUDelftiGEM2009_end}} | {{Template:TUDelftiGEM2009_end}} |
Revision as of 22:52, 24 July 2009
24 July 2009
Sriram
The cultures were grown in all the culture tubes [R0040, J23008, J23031, B0015, K081013, S03335, S03473, I714031, E0840, J23100]incubated yesterday except RBS[B0034] and pLacI[R0010], which may be because the colony we picked for those biobricks were not perfect. The plasmid DNA was extracted from all the grown cultures and stored in -20°C freezer.
The biobricks received from MIT for Delay [S03335, S03473] which were streaked yesterday have the colonies for future.
Tim Vos
Glycerol stocks were prepared for the remaining cultures grown in all the culture tubes [R0040, J23008, J23031, B0015, K081013, S03335, S03473, I714031, E0840, J23100]that were incubated yesterday and stored in -80°C freezer.
Daniel
Since the top10 competent cells newly prepared by us using the Openwetware protocol, didn't transform well for Tim Weenink we are in a bit crisis for competent cells. Anyway to make sure whether the cells work or not I did transformation of Biobricks RBS[B0034] and pLacI[R0010] in the newly created top10 competent cells and kept in drawer to grow in the weekend.
Orr
Today, I performed the mfold analysis to find out the secondary structures of the key3c and the lock3c. I also started looking at the COSMIC code that is intended to model conjugation. So far I only downloaded the source codes, and still need to find out how to run it.