Team:TUDelft/24 July 2009

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(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===
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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.