IGEM:Virginia 2012/Protocols/Isolating the Phage Genome

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Revision as of 09:25, 1 June 2012 by Alex Zorychta (talk | contribs) (New page: ==Overview== This is how to isolate the phage genome from a preparation of bacteriophages, specifically the ''Bordetella'' phage. ==Materials== * 10 mM EDTA * CsCl-banded phage * steril...)
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Overview

This is how to isolate the phage genome from a preparation of bacteriophages, specifically the Bordetella phage.

Materials

  • 10 mM EDTA
  • CsCl-banded phage
  • sterile tube
  • 100% ethanol
  • -20°C freezer
  • Centrifuge
  • 0.5 mL of 70% ethanol
  • TE Buffer

Procedure

  • Add 10 volumes of 10mM EDTA pH 8.0 to 1 volume of CsCl-banded phage in a sterile tube
  • Heat for 5 minutes at 65°C; let cool to room temperature
  • Add 2.5 volumes 100% ethanol; place in -20°C freezer for 20 minutes
  • Centrifuge: 10,000g for 5 minutes
  • Discard supernatant; rinse pellet with 0.5ml 70% ethanol; centrifuge again; discard supernatant; rinse pellet with 0.5ml 70% ethanol; centrifuge again; discard supernatant
  • Let pellet air dry at room temperature
  • Resuspend DNA in TE buffer; let DNA sit for several hours to go into solution; or, restriction digests can be performed immediately; store solution of DNA at -20°C for long-term storage (i.e. months) or at 4°C for short-term storage (i.e. 1-2 days)

Notes

Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input!


References

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