Haynes Lab:Notebook/Engineering PC-TFs/2013/02/05: Difference between revisions

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==Summary==
==2/5/13==
*  
<font size=3>'''Bacterial transformation'''</font>
* Added total volume (10.0 μL) to 50 μL chemically competent cells  (e.g., BL21) in a 2.0 mL tube.
* Incubated on ice for 2 min., heat shock at 42°C for exactly 45 sec., and placed on ice.
* Added 800 μL sterile SOC medium.
* Grow with shaking at 37°C for 30 min.(''Taped tubes to the shaker rack.'') 
* Pelleted the cells at top speed in a microcentrifuge for 3 min. at room temperature.
* Discarded the supernatant. Resuspended the cells in 100 μL LB + antibiotic.
* Plate cells on pre-warmed LB agar + antibiotic. (''I plated 100 μL of the cells. Then put beads on plates and shook.) Protocol didn't specify.'')  Grow overnight at 37°C.
* Check results tomorrow.
 
 
 




Revision as of 13:01, 9 February 2013

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2/5/13

Bacterial transformation

  • Added total volume (10.0 μL) to 50 μL chemically competent cells (e.g., BL21) in a 2.0 mL tube.
  • Incubated on ice for 2 min., heat shock at 42°C for exactly 45 sec., and placed on ice.
  • Added 800 μL sterile SOC medium.
  • Grow with shaking at 37°C for 30 min.(Taped tubes to the shaker rack.)
  • Pelleted the cells at top speed in a microcentrifuge for 3 min. at room temperature.
  • Discarded the supernatant. Resuspended the cells in 100 μL LB + antibiotic.
  • Plate cells on pre-warmed LB agar + antibiotic. (I plated 100 μL of the cells. Then put beads on plates and shook.) Protocol didn't specify.) Grow overnight at 37°C.
  • Check results tomorrow.




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