Dear Flow-ers, I have a colleague who wishes to analyze and sort cells that bear GFP and CFP (cyan fluor. protein) reporter constructs. Has anyone had experience doing this type of analysis with a Vantage SE and an Enterprise II laser (6 color config). I realize that using a 488 nm line is suboptimal for CFP, but is it feasible? Any info would be very much appreciated. Thanks, ---------------------- Andrew Herman Department of Pathology & Microbiology University of Bristol University Walk Bristol BS8 1TD Tel. +44 117 928 7511 Fax. +44 117 928 7896 A.Herman@bristol.ac.uk
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