Difference between revisions of "Preparation of Competent Cells for Electroporation"

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(Purpose)
(Protocol)
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== Protocol ==
 
== Protocol ==
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-Inoculate 5 mL of LB broth with bacterial cells to be transformed and grow overnight at 28 C with shaking
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 +
-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 10,000 rpm for 10 minutes and discard the supernatant
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 +
-Resuspend the cells in 35-40 mL of ice cold 10% glycerol and centrifuge at 10,000 rpm for 10 minutes, discard the supernatant
 +
 +
-Resuspend the cells in 18-20 mL of ice cold 10% glycerol and centrifuge at 10,000 rpm for 10 minutes, discard the supernatant
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 +
-Resuspend the cells in 350-400 microliters of ice cold 10% glycerol
 +
 +
-Aliquot the cells into small tubes
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 +
-The cells can be used right away or frozen in liquid nitrogen and stored for later use
  
 
== Notes ==
 
== Notes ==

Revision as of 14:55, 9 July 2015

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Purpose

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

Materials Needed

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 10,000 rpm for 10 minutes and discard the supernatant

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

-Resuspend the cells in 18-20 mL of ice cold 10% glycerol and centrifuge at 10,000 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

-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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