thanks but i've tried all that
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From: | Marcia Bentz <mb7x@virginia.edu> |
To: | histonet@pathology.swmed.edu |
Reply-To: | |
Date: | Fri, 30 Jul 1999 07:25:55 -0400 |
Content-Type: | text/plain; charset="us-ascii" |
Hi all,
Thanks for the suggestions. Problem is I've already done everything
everyone has suggested. At the moment I don't have access to any other
tissues. All the products are relatively new (exp. 3/200) but in
systematically eliminating things INCLUDING both primary and secondary
antibodies, the tissue is still staining. I have blocked for peroxidase,
which through testing I found wasn't necessary.
Here's what I've done:
substrate alone= no staining
blocking serum, ABC, substrate= inappropriate staining
blocking serum,avidin/biotin block (both 15 min and 30 min)= inappropriate
staining
blocking serum, avidin/biotin block, secondary with nml mouse serum in
addition to rabbit serum, ABC, substrate= inappropriate staining
I'm using frozen sections (mouse kidney) fixed 10 min with 4%
paraformaldehyde.
Pharmingen's rat anti-mouse TNF alpha, Vector avidin/biotin block, ABC
Elite rabbit anti-rat IgG secondary, and DAB
I want to again stress I'm gettting staining when omitting both primary and
secondary antibodies. I'm clueless....
Any more suggestions out there?
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