With FACS: Difference between revisions

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(Created page with "= For FACS = ---- *Finish the dissociation protocol *Resuspend in 150-200uL AMEM(0) *Send to FACS facility immediately **Book FACS machine F02 because it has both GFP and mChe...")
 
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*Resuspend in 50-100uL AMEM(0)
*Resuspend in 50-100uL AMEM(0)
*Count the cells
*Count the cells
**The sample is ready for downstream applications:
***[[For_scRNA-seq|scRNA-seq]]
***[[For_transplantation|cell transplantation]]

Revision as of 21:10, 18 July 2022

For FACS


  • Finish the dissociation protocol
  • Resuspend in 150-200uL AMEM(0)
  • Send to FACS facility immediately
    • Book FACS machine F02 because it has both GFP and mCherry lasers.
    • Normal setting: 85um nozzle with 0.7x FACS Flow for frog cells; 100um nozzle with 0.7x FACS Flow for axolotl cells.
  • Collect the cells into a 1.5mL tube with 700uL AMEM(0) inside. Note down the FACS count.
  • Spin down the cells. 300xrcf, 20 degree, 5 minutes.
  • Resuspend in 50-100uL AMEM(0)
  • Count the cells