Team:Columbia-Cooper-NYC/Electroporation
From 2012.igem.org
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# Place bacteria back into tube and add 100-200µl of LB | # Place bacteria back into tube and add 100-200µl of LB | ||
# Place samples in shaker for 37C for 1 hour | # Place samples in shaker for 37C for 1 hour | ||
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+ | Return to [[Team:Columbia-Cooper-NYC/Protocols|Protocols Page]] |
Revision as of 02:25, 3 October 2012
Electroporation Protocol
- The following is the electroporation protocol provided by bioline:
- Place cuvettes and competent cells into ice
- Add 1µl of DNA to 50µl of competent cells into 1mL cuvettes as quickly as possible
- Keep cuvettes in ice until electroporation
- Electroporate cells at 1800V
- Place bacteria back into tube and add 100-200µl of LB
- Place samples in shaker for 37C for 1 hour
Return to Protocols Page