Difference between revisions of "Transformation via Electroporation"
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== Protocol == | == Protocol == | ||
| + | -Set the electroporation apparatus to 1,8 kV, 25 microfarads, and the pulse controller to 200 omega | ||
| + | |||
| + | -Add 1.5 microliters of DNA to be transformed to 40 microliters of electrocompetent cells on ice and mix | ||
| + | |||
| + | -Transfer the DNA and cells to a pre-chilled 1 mm electroporation cuvette | ||
| + | |||
| + | -Wipe the cuvette with a kimwipe and place it into the sample chamber | ||
| + | |||
| + | -Deliver a pulse by pushing in charge button | ||
| + | |||
| + | -Remove the cuvette and ad 1 mL LB broth to the cuvette | ||
| + | |||
| + | -Transfer the broth and cells to a sterile tube and incubate for 2 hours at 28 C with shaking | ||
| + | |||
| + | -Place aliquots of the mixture on LB or NBY agar plates with the appropriate antibiotics for the cells | ||
| + | |||
| + | -Incubate at 28 C for 2 days | ||
== Notes == | == Notes == | ||
Revision as of 12:16, 13 July 2015
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Contents
Purpose
This protocol is used to transform electrocompetent cells with a plasmid.
Materials Needed
Protocol
-Set the electroporation apparatus to 1,8 kV, 25 microfarads, and the pulse controller to 200 omega
-Add 1.5 microliters of DNA to be transformed to 40 microliters of electrocompetent cells on ice and mix
-Transfer the DNA and cells to a pre-chilled 1 mm electroporation cuvette
-Wipe the cuvette with a kimwipe and place it into the sample chamber
-Deliver a pulse by pushing in charge button
-Remove the cuvette and ad 1 mL LB broth to the cuvette
-Transfer the broth and cells to a sterile tube and incubate for 2 hours at 28 C with shaking
-Place aliquots of the mixture on LB or NBY agar plates with the appropriate antibiotics for the cells
-Incubate at 28 C for 2 days
Notes
Papers where this or a similar method has been used
Related Ontology Terms
References
See Help:References for how to manage references in OMPwiki.
