Copenhagen/29 August 2011
From 2011.igem.org
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* Made Cam + IPTG plates | * Made Cam + IPTG plates | ||
+ | * Made plates with fungi and oximes, just to try it in another way. Put it in the 37 degrees incubator. | ||
Back to [[Team:Copenhagen/Notebook|notebook]] | Back to [[Team:Copenhagen/Notebook|notebook]] |
Latest revision as of 15:47, 30 August 2011
Monday
Labwork
- PCR purification of B1 after prefix-suffix-PCR. The purifactions are Nanodropped - B1 samples 3,4,5,8 and 10 looks fine.
- Digestions (1 h by 37 degrees or O/N)
* PSB1C3 with E + P * A2 in PSB1C3 with X + P * Expr.vector with P + S * B1 3,4,5,7 and 10 with E + P
- Purification of the digestions by using the PCR purifaction kit
- Ligations
* PSB1C3 + B1 samples 3,4,5,8 and 10 * Expr. vector + A2 * Selfmade Expr. vector + A2
- Transformation of ligations
- Made O/N cultures on: 2C9, UserB1 to Sequencing, UserB1 to growth and Control BL21 cells to growth.
- Made TB media and autoclaved bottles for tomorrow.
- Made Cam + IPTG plates
- Made plates with fungi and oximes, just to try it in another way. Put it in the 37 degrees incubator.
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