Fallon, Paul G. FallonPG at moffitt.usf.edu
Wed Dec 6 23:01:13 EST 2000

I am trying to attempting to stain a population of periferal blood with
a few different lineage panels including Erythroid for flow cytometric
analysis.  I am finding , however that my Glycophorin A stain is too
bright even when titrated down to 1µl/lamda.  I suspect nonspecific
binding.  Does anyone know of a method to block binding using ADP?

Paul Fallon

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