Template:SBB-Protocols Zymo3

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Revision as of 17:09, 24 February 2012 by Jonathan Kotker (Talk | contribs)
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Zymo Gel Purification

  • All spins until the drying step are 15 second full speed spins.
  1. cut out bands minimizing extra gel matter.
  2. put in ependorf tube and add 600uL of Zymo ADB buffer (brown bottle).
  3. heat at 55, shake and/or vortex until the gel has dissolved.
  4. If the DNA is <300bp add 250uL of isopropanol
  5. transfer into the Zymo column inside a collection tube (small clear guys)
  6. spin through, discard waste.
  7. Add 200 uL of Zymo Wash Buffer (which is basically 70% ethanol)
  8. spin through, discard waste.
  9. Add 200 uL of Zymo Wash Buffer
  10. spin through, discard waste.
  11. spin for 90 seconds, full speed to dry.
  12. elute with water into a fresh Eppendorf tube
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