Difference between revisions of "Transformation via Electroporation"
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== Materials Needed == | == Materials Needed == | ||
+ | -Electroporation apparatus | ||
+ | |||
+ | -1 mm electroporation cuvette | ||
+ | |||
+ | -micropipette | ||
+ | |||
+ | -LB broth | ||
+ | |||
+ | -Electrocompetent cells | ||
+ | |||
+ | -DNA | ||
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+ | -microfuge tubes | ||
+ | |||
+ | -ice | ||
+ | |||
+ | -kimwipes | ||
+ | |||
+ | -LB or NBY agar plates | ||
+ | |||
+ | -28 C incubator | ||
== Protocol == | == Protocol == |
Revision as of 12:32, 13 July 2015
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Contents
Purpose
This protocol is used to transform electrocompetent cells with a plasmid.
The electrocompetent cells are made using the protocol found on Preparation of Competent Cells for Electroporation.
Materials Needed
-Electroporation apparatus
-1 mm electroporation cuvette
-micropipette
-LB broth
-Electrocompetent cells
-DNA
-microfuge tubes
-ice
-kimwipes
-LB or NBY agar plates
-28 C incubator
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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