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Article #7784labeling thick sections
From: GREG VAUGHN MARTIN
Date: Thu, 18 May 1995 00:00
Date: Thu, 18 May 1995 00:00
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Hey Folks -- We are trying to immuno-label 20um frozen sections of fixed
liver through the entire section thickness. We have tried long (up to
overnight) incubation with primary antibody, included saponin or triton
(to 0.2%) and still have problems getting the antibodies into the middle
of the sections. Does anyone have any protocols that they have used
successfully for similar specimens? The tissue was embedded in
PVP-Sucrose prior to sectioning, and the sections can be either mounted
on slides or free-floating. Please respond directly to me at
gmartin@welchlink.welch.jhu.edu. Thanks in advance,
Greg Martin
Cell Biology and Anatomy
Johns Hopkins School of Med.
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X-Google-Language: ENGLISH,ASCII-7-bit X-Google-Thread: 114d69,a7b4fb9a964bcbd6,start X-Google-Attributes: gid114d69,public From: GREG VAUGHN MARTIN <gmartin@WELCHLINK.WELCH.JHU.EDU> Subject: labeling thick sections Date: 1995/05/18 Message-ID: <Pine.SOL.3.91.950518075154.12357A-100000@welchlink.welch.jhu.edu> X-Deja-AN: 102893578 sender: Confocal Microscopy List <CONFOCAL@UBVM.CC.BUFFALO.EDU> comments: Gated by NETNEWS@AUVM.AMERICAN.EDU content-type: TEXT/PLAIN; charset=US-ASCII content-length: 787 mime-version: 1.0 newsgroups: bit.listserv.confocal