Hello flow people, I have a question about autofluorescence that Iąd appreciate help with. If you see a lot of autofluorescence in samples prepared for intracellular staining (fixation, permeabilisation), is dye exclusion of dead cells a way to try and solve this? { The experiment prep involves enzymatic digestion(with collagenase and DNAse) and then percoll gradient of lung samples before intracellular staining.} Any help or advise and tips is much appreciated, Joanna Malaghan Institute Wellington NZ
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