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Team:ESBS-Strasbourg/17 July 2008
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== DryLab == | == DryLab == | ||
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| + | michi: | ||
| + | *found paper PMID: 18385157 which mutates TATA box and quantifies transcription :-) (King of the day) | ||
=== Modeling === | === Modeling === | ||
Revision as of 13:36, 18 July 2008
Contents |
DryLab
michi:
- found paper PMID: 18385157 which mutates TATA box and quantifies transcription :-) (King of the day)
Modeling
WetLab
- Results Transformation
- no clones for any of the three BioBricks
- clones for the LexA-BD plasmid --> useable for Miniprep
- counting:
- dh5a (Mariel) + pxj - KCM : 10^5 cfu/µg - dh5a (Mariel) + pxj - HS : 4*10^4 cfu/µg - dh5a + pxj - HS : 1.5*10^5 cfu/µg - Top10 + pxj - HS : 3.2*10^5 cfu/µg - db3.1 + pxj - HS : 3*10^4 cfu/µg
- The new BioBricks arrived in tubes with a sort of medium inside, we think they delivered us directly the bacteria with the BB-Plasmids inside, so we don't have to transform them on our own. Jippie!
- We made an overnight culture of, in LB(Amp):
- p1010 in pSB1A3
- BBa_c0012 (lacI)
- BBa_c0051 (lamda cI)
- BBa_j63001 (EYFP)
- We plated p1010 in pSB3K3 on LB Kan
- We made an overnight culture of, in LB(Amp):
- Digestion of the plasmid of the BBa_J63002(?) clone with XbaI and SpeI
- 1x double digestion
- 1x step by step digestion
- result:
- digestion seem to have work out in both cases
- but the gel shows a high contamination with low molecular RNA, so we know now that RNase is crutial in the eluation buffer
- the identity of the clone is still not verifified, because the size small fragement could be determinated
- but as the new BioBricks arrived today, there is no longer an interest to go on working on this clone
General
- Modeling meeting with Mr. Haich
Quote of the day
Marius loves Michis Kidneys!
