Preparation of Competent Cells for Electroporation: Difference between revisions

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== Purpose ==
== Purpose ==
This protocol is used for preparing competent cells to be used in electroporation transformation.
This protocol is used for preparing competent cells to be used in [[Transformation via Electroporation|electroporation transformation]].


== Materials Needed ==
== Materials Needed ==
-LB Broth
-28 C incubator
-37 C incubator
-centrifuge
-microfuge tubes
-ice cold 10% glycerol
-micropipette
-cells to be transformed


== Protocol ==
== Protocol ==
-Inoculate 5 mL of LB broth with bacterial cells to be transformed and grow overnight at 28 C with shaking
-Transfer 2 mL to 200 microliters of LB broth in a 1 liter flask and grow at 37 C with shaking until the optical density is 0.3-0.5
-Centrifuge the cells at 7,000 rpm for 10 minutes and discard the supernatant
-Resuspend the cells in 35-40 mL of ice cold 10% glycerol and centrifuge at 7,000 rpm for 10 minutes, discard the supernatant
-Resuspend the cells in 18-20 mL of ice cold 10% glycerol and centrifuge at 7,000 rpm for 10 minutes, discard the supernatant
-Resuspend the cells in 350-400 microliters of ice cold 10% glycerol
-Aliquot the cells into small tubes of about 40 microliters each
-The cells can be used right away or frozen in liquid nitrogen and stored for later use


== Notes ==
== Notes ==

Latest revision as of 20:07, 20 July 2015

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Purpose

This protocol is used for preparing competent cells to be used in electroporation transformation.

Materials Needed

-LB Broth

-28 C incubator

-37 C incubator

-centrifuge

-microfuge tubes

-ice cold 10% glycerol

-micropipette

-cells to be transformed

Protocol

-Inoculate 5 mL of LB broth with bacterial cells to be transformed and grow overnight at 28 C with shaking

-Transfer 2 mL to 200 microliters of LB broth in a 1 liter flask and grow at 37 C with shaking until the optical density is 0.3-0.5

-Centrifuge the cells at 7,000 rpm for 10 minutes and discard the supernatant

-Resuspend the cells in 35-40 mL of ice cold 10% glycerol and centrifuge at 7,000 rpm for 10 minutes, discard the supernatant

-Resuspend the cells in 18-20 mL of ice cold 10% glycerol and centrifuge at 7,000 rpm for 10 minutes, discard the supernatant

-Resuspend the cells in 350-400 microliters of ice cold 10% glycerol

-Aliquot the cells into small tubes of about 40 microliters each

-The cells can be used right away or frozen in liquid nitrogen and stored for later use

Notes

Papers where this or a similar method has been used

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Related Ontology Terms

References

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