Re: Disappearing Cytoplasm!!
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From: | "Tim Morken" <timcdc@hotmail.com> |
To: | histoNet@pathology.swmed.edu |
Reply-To: | |
Date: | Tue, 21 Sep 1999 07:50:04 EDT |
Content-Type: | text/plain; format=flowed |
It sounds like you have some extraction of the cytoplasm. Why not fix
directly after cutting? There is not really any need to dry so long before
fixing. You can use ice-cold formalin which can be kept right in the
cryostat cabinet. Cut and drop the slides in.
Tim Morken, B.A., EMT(MSA), HTL(ASCP)
Infectious Disease Pathology
Centers for Disease Control
MS-G32
1600 Clifton Rd.
Atlanta, GA 30333
USA
email: tim9@cdc.gov
timcdc@hotmail.com
Phone: (404) 639-3964
FAX: (404)639-3043
----Original Message Follows----
From: Bruce Abaloz <b.abaloz@zoology.unimelb.edu.au>
To: histoNet@pathology.swmed.edu
CC: s.cuff@microbiology.unimelb.edu.au
Subject: Disappearing Cytoplasm!!
Date: Mon, 20 Sep 1999 17:22:03 +1000
Hi all....I'm a student here @ the Uni.of Melbourne & am freezing fresh
liver & spleen (mouse), floating the OCT covered specimen in a boat in
liquid nitrogen
until OCT is a solid block then I drop it all into the liquid nitrogen. I
store it @ -70C until ready to cut in the cryostat.I am using Histogrip
slides & cut @ 6 microns @ -10C.I let it dry @ room temp.for 1/2 hr.- 2
hrs.then fix in 10% NBF for 10 min. rinsing X3 in PBS. after which I
transfer to DH2O to transport to the Histology Lab. for H&E staining. I have
no problem with the stain but the sections after staining, look as if the
cytoplasm has been "dehydrated away".Can
anyone advise me on what "to do" or what I'm doing wrong. I've also tried
Acetone fixation (10 min.@ RT) with the same result??????????? I look
forward to your replies & THANKYOU in advance.........Simone Cuff.
--
BRUCE ABALOZ
HISTOLOGIST
DEPARTMENT of ZOOLOGY * ph: +61 3 93446282
The UNIVERSITY of MELBOURNE * fax: +61 3 93447909
Parkville Victoria.3052 * email: b.abaloz@zoology.unimelb.edu.au
AUSTRALIA.
IF YOU WANT TO BE HAPPY......BE!!
I DO NOT SEEK............I FIND!!
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