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background

Kathleen Gajewski sa08383 at ODIN.MDACC.TMC.EDU
Thu Jan 28 18:20:09 EST 1999


I've been trying fluorescent double stainings on whole mount embryos, and 
I've been having background problems.  The green ones (FITC, Cy2) seem to 
be the worst.  Can anybody tell me how to knock down the background?  Or does 
confocal microscopy do the trick?

				Thanks,  Kathleen Gajewski





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