Omit  the  primary  antibody,  or you can always buy a "negative cont   
rol".   It  does  the  same  thing  as  just incubating the section in
   buffer=  for  the  same  time as the positive control with the primary
   (and  it  saves  a=  ton  of money!).  If you need a specific negative
   control tissue, this= is going to be different for every antibody.

   = Sarah Goebel, B.A., HT (ASCP)
   Histotechnician

   XBiotech USA Inc.

   8201 East Riverside Dr. Bldg 4 Suite 100

   
   Austin, Texas = ; 78744

   (512)386-5107

   -------- Original Message --------
   Subject: Immunofluorescence QC
   From: "Nails, Felton" <[1]fln= a...@texaschildrens.org>
   Date: Tue, August 31, 2010 10:26 am
   To:  "'[2]sgoe...@xbiotech.com'"  &l= t;[3]sgoe...@xbiotech.com>, "Ch   akib
   Boussahmain" <[4]chak_...@yahoo.com>
   Cc: "[5]histo...@lists.ut= southwestern.edu"
   <[6]histo...@lists.uts= outhwestern.edu>
   We have always done IF's utilizing internal positive controls. The new
   CAP  = checklist is now requiring positive and negative controls. What
   are you guy= s doing for negative controls?
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References

   1. 3D"mailto:flna...@texaschildrens.org";
   2. 3D"mailto:sgoe...@xbiotech.com";
   3. 3D"mailto:sgoe...@xbiotech.com";
   4. 3D"mailto:chak_...@yahoo.com";
   5. 3D"mailto:histonet@lists.utsouthwestern.edu";
   6. 3D"mailto:histonet@lists.utsouthwestern.edu";
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