>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