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Can anyone advise us on the best method for approaching this problem
by flow cytometry? Doesn't someone sell beads which are standardized
as to the amount of fluorescence on them? Can we use these as
internal standards to control for experiment-to-experiment
variability in fluorscence intensity of the antigen density of cells?
Steve Shivers
Bone Marrow Transplant Program
Moffitt Cancer Center
at the University of South Florida
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CD-ROM Vol 3 was produced by Monica M. Shively and other staff at the
Purdue University Cytometry Laboratories and distributed free of charge
as an educational service to the cytometry community.
If you have any comments please direct them to
Dr. J. Paul Robinson, Professor & Director,
PUCL, Purdue University, West Lafayette, IN 47907.
Phone: (765)-494-0757;
FAX(765) 494-0517;
Web