Difference between revisions of "Team:Paris Saclay/Notebook/July/27"

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We obtained transformed bacteria for every conditions made yesterday (except for controls).
 
We obtained transformed bacteria for every conditions made yesterday (except for controls).
[[File:T--Paris_Saclay--160711_characterization_K13-TAA.jpg|400px|thumb|right|Colonies of BL21|pcl_TAA and K1372001]]
+
[[File:T--Paris_Saclay--160711_characterization_K13-TAA.jpg|150px|thumb|right|Colonies of BL21|pcl_TAA and K1372001]]
 
   
 
   
 
We wanted to have glycerol stock of our transformed bacteria so we had to make a pre-culture. Cells were put in 2mL of LB + Streptomycin (50µg/mL) + Chloramphenicol (30µg/mL) medium. They were incubated overnight at 37°C, 180 rpm.  
 
We wanted to have glycerol stock of our transformed bacteria so we had to make a pre-culture. Cells were put in 2mL of LB + Streptomycin (50µg/mL) + Chloramphenicol (30µg/mL) medium. They were incubated overnight at 37°C, 180 rpm.  

Revision as of 12:35, 27 July 2016

Wednesday 27th July

Lab work

Visualization

==

By


Biobrick Characterization

BL21 electrocompetent cells preparation for glycerol preparation

By Charlène

We obtained transformed bacteria for every conditions made yesterday (except for controls).

pcl_TAA and K1372001

We wanted to have glycerol stock of our transformed bacteria so we had to make a pre-culture. Cells were put in 2mL of LB + Streptomycin (50µg/mL) + Chloramphenicol (30µg/mL) medium. They were incubated overnight at 37°C, 180 rpm.