>We are planning to try to analyze integrins on the surface of cells grown
>on beads. We would like to be able to label the integrins that are being
>used by the cells to adhere to the beads while they are still adhering to
>the beads.
>Anyone ever tried anything like this? Like with superpermeable beads?
>
>Also, what is the upper size limit for analysis with FACScan? All we care
>about are the fluorescence signals.
>
>Thanks in advance.
>
>Debbie Berglund
>Microbiology
>Montana State University
>Bozeman, MT 59717
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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
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PUCL, Purdue University, West Lafayette, IN 47907.
Phone: (765)-494-0757;
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