Re: Secondary staining

From: Simon Monard (smonard@trudeauinstitute.org)
Date: Fri Mar 16 2001 - 09:35:57 EST


>>> Scott Tighe <stighe@zoo.uvm.edu> - 3/15/2001 3:41 PM >>>

Greeting all:

I have a situation in which I am detecting a cytokine that its
expression is low. My question is, we are using PE as our secondary
stain and I am wondering if I use a brighter stain if my negative and
positive peaks will separate more? Is this a reasonable assumption and
if so, what stain would be best?

Scott Tighe
Vermont Cancer Center



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