Hello, I was wondering if anyone can come up with solutions to tackle a recurring problem we have with analyzing monocyte and neutrophil markers using flow cytometry. The isotype controls rarely fall within the lower left quadrant when we look at these cells. This becomes a big problem for setting gates to analyze samples. For Lymphocyte populations on the other hand, isotype controls are really tight. Any suggestions anyone? Thanks in advance Kanika Ghai Graduate Student The Ohio State UniversityReceived on Mon Mar 28 12:38:00 2005
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