Hi everyone, I have a question with respect to the feasibility of fixing cells for analysis of oxidative burst and phagocytosis. I am using Hydroethidine to assess oxidative burst in monocytes and neutrophils (whole blood) following PMA stimulation. The phagocytosis is assessed via FITC labelled opsonised zymosan. Is it possible to fix these cells (if so, what's the best way) to allow for analysis the day after staining? Will the dye leak from cells after fixation? Thanks in advance for your help Rebecca Court
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