Culturing S2 Cells

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Revision as of 13:23, 3 August 2009 by Davebridges (Talk | contribs)

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Materials

  • S2 cells see Freezing and Thawing S2 Cells
  • Sf-900 II SFM medium (Invitrogen, cat. no. 10902) - stocked downstairs
  • Penicillin/streptomycin 50X mix (Invitrogen, cat. no. 15240062) - stocked downstairs
  • Insect Cell Media. Filter together Media (500 mL) and Pen/Strep (10 mL) into a tissue culture bottle

Protocol

  • Typically cells are split every 3-4 days at a ratio of 1:5 and grown at 25C
  • After 2-3 days the cells become slightly less adherent.
  1. To split, gently aspirate the media (some cells will have detached from the plate surface)
  2. Pipet a gentle stream of media over the surface of the plate (5 mL for normal passage)
  3. Add 10 mL to fresh 10 cm dishes
  4. Add 1 mL of detached cells to each new plate

Knockdown

References

see PMID 11752672 and PMID 18388942