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Team:Freiburg/Notebook/8 June
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{| border="1" align="center" style="text-align:center;" | {| border="1" align="center" style="text-align:center;" | ||
|'''part''' | |'''part''' | ||
| - | |'''location(p=plate)''' | + | |'''location(p=plate) ''' |
| - | |'''resistance''' | + | |'''resistance ''' |
|'''info''' | |'''info''' | ||
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|P3, 24E | |P3, 24E | ||
|amp | |amp | ||
| - | |Lambda phage lysis device - no promoter, This part is in BBb Format. It is flanked by BamHI and BglII sites instead of XbaI and SpeI. | + | |Lambda phage lysis device - no promoter, This part is in BBb Format.<br/>It is flanked by BamHI and BglII sites instead of XbaI and SpeI. |
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Revision as of 10:38, 8 July 2011
Protein modelling and amplification of parts
Investigators:
Protein modelling with pymol: Rüdiger
Amplification of different parts: Julia and Jacob
antibiotics plates:
1oo mg/ml Ampizilin (100 microliter per plate)
1oo mikroliter H2O + 2 microliter Cm
1oo mikroliter H2O + 40 microliter Tet
1oo mikroliter H2O + 10 microliter Kan
| part | location(p=plate) | resistance | info |
| BBa_K098995 | P3, 1E | Amp | heat sensitive cI QPI with high promoter |
| BBa_K112022 | P3, 24E | amp | Lambda phage lysis device - no promoter, This part is in BBb Format. It is flanked by BamHI and BglII sites instead of XbaI and SpeI. |
