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if you culture ips cells in feeder, the collagenase IV is a good choice. But for feeder free, Accutase and dispase is not good. I suggest you use 0.5 mM EDTA in PBS. for 33mm dish, add 2ml of 0.5 mM EDTA, incubate at room temperature for 3-5 minutes, aspirate the EDTA. Then add 1 ml of medium using 1 ml pipet, pipet up and down to disassociate the ips cell and transfer into a new tube.
2 H( c$ y6 r. Z4 \. h( l) C, q5 ?6 V1 r- P( l) |- ^ O
补充内容 (2012-9-22 10:12):
$ ~/ \5 W9 }' ~" J1 x( @% E8 Q. ^* sIn our lab, it works well. this protocol from James A Thomson laboratory |
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