User:Karmella Haynes/Notebook/PcTF Genomics/2012/12/18: Difference between revisions

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# "K562 1": 1:8 dilution cells, no DNA
# "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
* Collect 1 mL cells from 10 cm plate into 2.0 mL microfuge tubes (did this 4x for each culture); discard remainder of culture
* Pellet cells at r.t./ 5 min./ 3000 rpm
* Pellet cells at r.t./ 5 min./ 3000 rpm
* Discard supernatant
* Discard supernatant

Revision as of 20:23, 4 June 2014

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12/18/12

  • 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 (did this 4x for each culture); discard remainder of culture
  • Pellet cells at r.t./ 5 min./ 3000 rpm
  • Discard supernatant
  • Resuspend pellet in 500 μL TRIzol
  • Store at -80°C for next steps (Carly)



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