Hi all, I recently started to work with HACAT cells.
but it was very difficult to subculture.
Does anybody have any suggestions as to what is causing this problem of the cells
or has anybody had the same problems and managed to overcome them?
Ex: change trypsin concentrate(%) or add something to medium and PBS buffer.
Thanks for helping!
It was very difficult to subculture HaCaT
Started by jim chen, Jul 10 2009 11:54 PM
2 replies to this topic
#1
Posted 10 July 2009 - 11:54 PM
#2
Posted 13 July 2009 - 06:02 AM
subculture - is that the same as splitting?
if so - no probs whatsoever
your questions a bit vague - whats the problem - do they shout obcenities at you?
dom
if so - no probs whatsoever
your questions a bit vague - whats the problem - do they shout obcenities at you?
dom
#3
Posted 10 October 2012 - 03:17 PM
The Hacat cells I have been working with are easy to subculture. I don't have any problem with them. Can you elaborate what you have done, and the passage of the cells you are using. It matters.













