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Kathleen Gajewski sa08383 at ODIN.MDACC.TMC.EDU
Mon Oct 26 20:03:23 EST 1998

One more question for all the Flypeople:
	I have just started playing with fluorescent tagged secondary 
antibodies (Texas Red), and although I can see the expected staining 
pattern, I'm getting some background.  I would like to double stain with 
FITC, but I'm afraid the red background would screw up my results.  What 
I need to know from those of you who regularly do red/green double 
staining is, how do you knock down the background?  I've tried a more 
complex blocking solution and preadsorbing the secondary Ab against fixed 
embryos, but I'm having no success.  Any advice will be greatly appreciated!

					Thanks again,
					Kathleen Gajewski

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