I am trying to determine apoptosis induction on adherent tumor cells. I used annexin/PI staining, however the background of annexin staining in untreated cells was up to 20 %. I am concerned that the cell dissociation buffer already induces apoptosis. I also tried IHC, but was loosing a lot of cells when I was trying to fix them. Does anybody have a good protocol how to do apoptosis measurements in adherent cells? thank you, Anke
This archive was generated by hypermail 2b29 : Sun Jan 05 2003 - 19:01:19 EST