发布时间:2019-04-26 17:33 原文链接: ThawingCells(Schreibersprotocol)

  1. Thaw vial quickly in 37癈 water. Caution - vial can explode.

  2. Transfer cells to sterile, 15 mL centrifuge tube.

  3. Add 50 祃 warm FBS (fetal bovine serum, heat inactivated), wait 1 minute.

  4. Add 100 祃 FBS, wait 1 minute.

  5. Add 200 祃 FBS, wait 1 minute.

  6. Add 400 祃 FBS, wait 1 minute.

  7. Add 800 祃 FBS, wait 1 minute.

  8. Centrifuge for 5 minutes at 1000 rpm.

  9. After aspirating supernatant, resuspend in 5 - 6 mL warm media.

  10. Transfer to T 25 (25 cm2 flask).

  11. Incubate at 37癈 and 5% CO2 with top of flask loose.

  12. Next day, check that cells are viable and attached. Pour off or aspirate media. Add 5 - 6 mL fresh warm media.

  13. Passage into T75 when cells become confluent (some cells, like RCHO-1 never become confluent)