y slides/tissue samples
minimum for predictive markers, then you do the correlation. Keep everything
for CAP.
Joelle Weaver MAOM, HTL (ASCP) QIHC
> From: cda...@che-east.org
> To: histonet@lists.utsouthwestern.edu
> Date: Tue, 25 Mar 2014 09:51:07 -0400
> Subject: [Histonet] IHC antib
Will you help me? I understand we are to use the known positives controls that
the manufactures' recommends in the package insert when optimizing the stains,
but I need to know what is your general procedure for optimizing (how many
different staining protocols do you test) and validating a new
