All, I have started using Dynal strepavidin coated paramagnetic beads to detect proteins in cell homogenates by flow cytometry. I am pretty happy with the initial results, but I was wondering if people could tell me about the advantages of other beads for such assays. The paramagnetic nature of these beads make them easy to wash, but they are quite small (~1 micron?) and I was wondering if larger beads might have greater binding capacities and give me a lower detection limit for my protein? Can anyone inform me? Thanks, Mike -- ________________________________________________________ / Michael J. Herron, U of MN, Dept. of Pediatrics/BMT / / herro001@umn.edu / / 612-626-4321 Mpls MN 55455 / /_______________________________________________________/
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