[Histonet] double trouble

[Gayle Callis]

Hopefully Chris van der Loos is looking in on this and will send the person 
who needs to do double IHC.  He just published a very useful method in 
Journal of Histotechnology on this subject where the first antibody complex 
is removed, leaving behind chromogen after a retrieval method followed by 
the second antibody complex with a different chromogen.  He may have a pdf 
of his publication available.

Gayle M. Callis
HTL/HT/MT(ASCP)
----- Original Message ----- 
From: "Paula Pierce" <contact <@t> excaliburpathology.com>
To: "Edwards, R.E." <ree3 <@t> leicester.ac.uk>; "Histonet" 
<histonet <@t> lists.utsouthwestern.edu>
Sent: Monday, November 03, 2008 7:23 AM
Subject: Re: [Histonet] double trouble


Incubate with one antibody and use DAB as the chromagen, then go back and 
incubate with the second antibody and use a colored chromagen such as AEC.


Paula



----- Original Message ----
From: "Edwards, R.E.." <ree3 <@t> leicester.ac.uk>
To: histonet <histonet <@t> lists.utsouthwestern.edu>
Sent: Monday, November 3, 2008 8:08:46 AM
Subject: [Histonet] double trouble


OK chaps, which in your opinion is the best double labelling method when one 
is using primary antibodies raised in the same species, I am aware that 
Vector labs supply such a kit; many thanks..

Cheers
Richard Edwards
University of Leicester

U.K....


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