User:Karmella Haynes/Notebook/PcTF Genomics/2012/12/18

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Revision as of 15:05, 18 December 2012 by Karmella Haynes (talk | contribs) (mm/dd/yy)
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mm/dd/yy

  • TriZOL-RNeasy prep: lyse cells in TriZOL; store at -80°C

TriZOL-RNeasy prep

  1. "K562 1": 1:2 dilution cells, +DNA
  2. "K562 1": 1:2 dilution cells, no DNA
  3. "K562 1": 1:4 dilution cells, +DNA
  4. "K562 1": 1:4 dilution cells, no DNA
  5. "K562 1": 1:8 dilution cells, +DNA
  6. "K562 1": 1:8 dilution cells, no DNA
  • Collect 1 mL cells from 10 cm plate into 2.0 mL microfuge tubes (4x); discard remainder of culture
  • Pellet cells at r.t./ 3 min./ 2000 rpm
  • Discard supernatant
  • Resuspend pellet in 500 μL TriZOL
  • Store at -80°C for next steps (Carly)