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I guess this is essentially a rare event problem--does anyone have any
ideas? The embarassing part is that they can see these sperm clearly on a
fluorescence scope, but flow seemed to be a more objective way of
comparing all of the sample rather than one frame of a slide. Now they're
considering counts of confocal images, but would much prefer a faster flow
approach. Thanks in advance for any info you can send,
Steve Hilliard
Cell Analysis Facility, Univ. of GA : "Be good and you will
internet: hilliard@zookeeper.zoo.uga.edu : be lonesome"
voice: (706)542-9474 :
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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