[Cytometry] multiple negatives for comp in Diva?
carol.norris at uconn.edu
Thu Feb 6 11:40:14 EST 2014
Hi Flow Gurus,
We have lots of folks combining GFP-expressing cells with antibody labeling, and I’d like to get more of them using comp beads for the antibody controls. There doesn’t seem to be a way to use GFP-negative cells for the GFP comp control and unstained beads for the antibody comp controls in Diva. Are unlabeled cells OK to use as a universal negative? The other option would be to transfer the data to FlowJo to get a comp matrix, and then transfer the comp values back into Diva.
Carol E. Norris, Ph.D
Flow Cytometry/Confocal Microscopy Facility
University of Connecticut Unit 3149
91 N. Eagleville Rd
Storrs, CT 06269-3149
Phone (860) 486-3080
Fax (860) 486-5005
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