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You might try running your mixture of bead / cells through a known pore size
filter/mesh prior to analysis and go from there. The fluorescence is
indepedent.
Regards
Tony Ward
Assoc Product Manager
BDIS
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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