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
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