Dear Flowers: I have an investigator here who is doing cotransfection using YFP/RFP. Under the microscope he can clearly see the positive RFP cells. However maximal excitation for RFP is about 585 so I 'm getting a very weak signal in the FL2 channel. Also the YFP signal is so bright it tails into the double positive quadrant. What is the best combination of fluorescent proteins to use to get optimal separation? Thanks in advance for your help. Jackie Saleh Aventis Pharmaceuticals jacqueline.saleh@aventis.com
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