Haynes Lab:Notebook/Jan/2015/08/31: Difference between revisions

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*Make 1 new T-75 at a 1:10 dilution
*Make 1 new T-75 at a 1:10 dilution
*Passage number: 5
*Passage number: 5


* 6-well plate - U2OS
* 6-well plate - U2OS

Latest revision as of 01:06, 27 September 2017

Project name Main project page
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Cell Culture

  • Passaging - U2OS, split PS5 --> PS6
  • 6-well plate - U2OS
  • Passaging - U2OS
  • Protocol: Splitting Cells
  • Cell culture medium is: McCoy's 5A, 10% FBS (tet-free), 1% P/S
  • Use 90-100% confluent T-75
  • Make 1 new T-75 at a 1:10 dilution
  • Passage number: 5


  • 6-well plate - U2OS
  • Use same resuspension from old flask in Passaging - U2OS
  • Starting with: 10E6/10 mL = 1.0E6/1 mL stock cell resuspension concentration
  • Desired cells/ well in new 6-well plate = 2.5E5 (250k) cells in 4.0 mL medium
  • Amount of starting culture(x) to use: x = (1.0E6 cells / 1 mL) / 2.5E5 cells = 0.25 mL stock cell resuspension per well
  • Amount of fresh medium to use: 4.0 mL final volume - 0.25 mL stock cells = 3.75 mL fresh medium per well
  • Make a batch of diluted cells for new 6-well plate:
  • Into a sterile 50 mL conical add...
  • (6 wells + 1 pipetting error) x 0.25 mL stock cells = 1.75 mL stock cells
  • (6 wells + 1 pipetting error) x 3.75 mL fresh medium = 26.25 mL fresh medium


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