Difference between revisions of "Preparing chemically competent cells (Inoue)"

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(Related topics & references)
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#Inoue90 pmid=2265755
#Inoue90 pmid=2265755
#Hengen96 pmid=8851666
[[Category:E.Coli Protocol]]
[[Category:E.Coli Protocol]]

Revision as of 07:43, 12 April 2006


  • Plate of cells streaked for single colonies
  • SOB
  • Ice
  • TB buffer
  • DMSO
  • Dry Ice (or liquid nitrogen)

Glassware & equipment

  • 2 liter erlenmeyer flask (no detergent residue, rinse with 70% ethanol and DI water)
  • 220 ml conical centrifuge tubes BD 35 2075
  • Eppendorf 5410R refrigerated centrifuge with conical adapters


  1. Pick a 10 - 12 large single colonies (2-3 mm dia) from your source plate and inoculate 500 ml of sterile SOB medium (do not use LB) in a 2 liter flask.
  2. Grow to an OD of 0.6 with vigorous shaking (200-250 rpm) at 18 degrees (important)
  3. Prechill the centrifuge to 4 degrees
  4. Remove from the incubator and place on ice for 10 minutes
  5. Transfer to two 220 ml centrifuge tubes and spin at 3220 x g for 10 minutes at 4 degrees
  6. Drain the medium and resuspend each pellet first in 5 ml of ice cold TB. Add an additional 75 ml of cold TB buffer and resuspend.
  7. Place on ice for 10 minutes
  8. Spin down as above.
  9. Resuspend each pellet in 20 ml of cold TB
  10. Add DMSO to a final concentration of 7%
  11. Incubate on ice for 10 minutes
  12. Dispense cells into pre-chilled tubes
  13. Freeze cells in a dry ice / ethanol bath and store at -80 degrees indefinitely

Related topics & references

Original protocol from Inoue et al. [1].

  1. Inoue H, Nojima H, and Okayama H. High efficiency transformation of Escherichia coli with plasmids. Gene. 1990 Nov 30;96(1):23-8. PubMed ID:2265755 | HubMed [Inoue90]
  2. Hengen PN. Methods and reagents. preparing ultra-competent Escherichia coli. Trends Biochem Sci. 1996 Feb;21(2):75-6. PubMed ID:8851666 | HubMed [Hengen96]
All Medline abstracts: PubMed | HubMed