[Histonet] alkaline phosphatase
Connolly, Brett M
brett_connolly <@t> merck.com
Wed Feb 18 14:23:44 CST 2004
Martin,
Another possibility comes to mind. You might consider changing the
peroxidase substrate. I have used TrueBlue Peroxidase Substrate from
Kirkegaard & Perry Laboratories, it's more sensitive than DAB and if you
play with the conditions you can end up with a turquoise reaction product.
http://www.kpl.com/webpromotions/index.cfm?pID=60
Regards,
Brett
Brett M. Connolly, Ph.D.
Merck & Co., Inc.
MRL, Imaging Research
WP26A-3000
PO Box 4
West Point, PA 19486
PH 215-652-2501
fax. 215-652-2075
e-mail. brett_connolly <@t> merck.com
-----Original Message-----
From: histonet-bounces <@t> lists.utsouthwestern.edu
[mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of Martin Weber
Sent: Wednesday, February 18, 2004 2:20 PM
To: histonet <@t> lists.utsouthwestern.edu
Subject: [Histonet] alkaline phosphatase
Hello,
I might need to do a dual staing procedure on paraformaldehyde fixed
fresh frozen sections. One marker will be stained with peroxidase (DAB).
As a second marker for IHC I read about alkaline phosphatase (FastRed)
which gives rise to a red color in addition to the brown color of the
peroxidase staining. To me this combination seems to be a little bit
unfortunate because the colors are sort of overlapping.
Does anybody know of an alternative and complimentary method for dual
staining which might give rise to a different color other than red ?
Unfortunately due to special circumstances Immunofluorecence is not an
option.
Any help is much appreciated. Thanks a lot !
Martin Weber
The Scripps Research Institute
Dept. of Molecular and Experimental Medicine
10550 North Torey Pines Road
La Jolla, 92037
Phone: 858-784-8612
Fax: 858-784-2030
E-Mail: maweber <@t> scripps.edu
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