Transformation via Electroporation

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Revision as of 12:16, 13 July 2015 by Tkveton (talk | contribs) (Protocol)

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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

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