[Histonet] cap ihc info

[patsy ruegg]

This is an ongoing issue in IHC, when dealing with limited tissue how can we
afford to use up sections for negative controls on each block.  I haven't
been updated on this for awhile, just wondering what is happening in the
real world, are you including a negative (isotype matched reagent in place
of the primary antibody) for each block even when it is a small biopsy
specimen.
Patsy 

Patsy Ruegg, HT(ASCP)QIHC
IHCtech
12635 Montview Blvd. #216
Aurora, CO 80010
720-859-4060
fax 720-859-4110
pruegg <@t> ihctech.net
www.ihctech.net 
-----Original Message-----
From: histonet-bounces <@t> lists.utsouthwestern.edu
[mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of Roxanne Soto
Sent: Friday, December 09, 2005 8:19 AM
To: histonet <@t> lists.utsouthwestern.edu
Subject: [Histonet] cap ihc info


       ______________________________________________________________

     >I  have  a  question  about  a particular IHC that I do on a daily
     basis. I do a PIN-4 cocktail
     >stain  on  prostate  cores. This cocktail contains p63, CK903, and
     P504S. My question is, do I
     >need to perform a negative control?
     >Right  now  we are not CAP certified, but we are looking to become
     certified. CLIA only
     >requires one negative per case, instead of one negative per block.
     We deal with very tiny
     >cores  and  I  am  currently following the CLIA guidelines in this
     matter. However, we are
     >looking  to  automate  and  work  on  CAP  accreditation  and this
     negative factor would greatly
     >increase  our volume and therefor would mean that we would need to
     get a stainer to
     >accommodate the volume.
     >I  know that whenever I do a CK903, I do not do a negative because
     the tissue has built in
     >controls. Is this now null and void because of the racemase?
     >Please advice.
     >Thank you
     >Roxanne Soto HT(ASCP)
     >Tampa
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