Team:Cambridge/Protocols/Overnight Culture

From 2011.igem.org

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;  '''1.''':Media preparation: Add 1 μl of 1000x concentrated ampicillin for each 1 ml of liquid broth. Be careful to keep the medium sterile especially if not adding an antibiotic, to avoid contamination.
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*Media preparation: Add 1 μl of 1000x concentrated ampicillin for each 1 ml of liquid broth. Be careful to keep the medium sterile especially if not adding an antibiotic, to avoid contamination.
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;  '''2.''' Label on the plates the colonies you wish to culture.
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*Label on the plates the colonies you wish to culture.
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;  '''3.''' Pour 30 ml of the prepared medium into a falcon tube labelled to match the desired colony.
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*Pour 30 ml of the prepared medium into a falcon tube labelled to match the desired colony.
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;  '''4.''' Using a sterile loop, transfer the colony to the liquid medium in the tube.
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*Using a sterile loop, transfer the colony to the liquid medium in the tube.
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;  '''5.''' Incubate for 14-16h in a shaking incubator at 37 degrees.
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*Incubate for 14-16h in a shaking incubator at 37 degrees.
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;  '''6.''' To pellet the bacteria, make sure the tubes are balanced and centrifuge for at least 15 minutes at 3000 rpm.
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*To pellet the bacteria, make sure the tubes are balanced and centrifuge for at least 15 minutes at 3000 rpm.
===Safety===
===Safety===
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All materials coming into contact with transgenic E. coli must be autoclaved.
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All materials that come into contact with transgenic E. coli must be autoclaved.
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{{Template:Team:Cambridge/CAM_2011_TEMPLATE_FOOT}}

Revision as of 16:06, 10 August 2011

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E. coli Cell Culture

Method to prepare a culture of E. coli in liquid medium for DNA extraction.

Method

This is the method for overnight preparation of a 30ml cell culture of ampicillin-resistant E. coli. For a smaller culture volumes must be adjusted and as well as the incubation time. Most transgenic bacteria should have resistance to some antibiotic which should be substituted for ampicillin.


  • Media preparation: Add 1 μl of 1000x concentrated ampicillin for each 1 ml of liquid broth. Be careful to keep the medium sterile especially if not adding an antibiotic, to avoid contamination.
  • Label on the plates the colonies you wish to culture.
  • Pour 30 ml of the prepared medium into a falcon tube labelled to match the desired colony.
  • Using a sterile loop, transfer the colony to the liquid medium in the tube.
  • Incubate for 14-16h in a shaking incubator at 37 degrees.
  • To pellet the bacteria, make sure the tubes are balanced and centrifuge for at least 15 minutes at 3000 rpm.

Safety

All materials that come into contact with transgenic E. coli must be autoclaved.


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