Hey All, I Would like to let folks know that I have brought the high background in J774A.1 (FL2 peak channel of close to 200) to acceptable levels (P.Ch.of around 5)and still have the ability to detect my positive control marker. The main culprit seemed to be FL2 spill over into FL1 and FL3 which I was able to compensate for. A change to media w/out phenol red seemed to help as well. Thanks again for the helpful suggestions. Chris Reed Senior in Biology Washington State University
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