[Histonet] RE: Tissue fixation help

[Rittman, Barry R]

Several reasons
Perhaps the major one is that frozen and paraffin sections of equal
thickness show a different morphology. Frozen tissue is said to have a
general shrinkage of soft tissues of around 2-5% while in paraffin this
may reach 25 -30%.  Sections of equal thickness therefore contain
different volumes of tissue and will stain to different degrees. The
final image therefore does not always allow for easy comparison.
Barry

-----Original Message-----
From: histonet-bounces <@t> lists.utsouthwestern.edu
[mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of Charles
Scouten
Sent: Monday, October 03, 2005 2:54 PM
To: Patsy Ruegg; C.M. van der Loos; Histonet <@t> lists.utsouthwestern.edu
Subject: RE: [Histonet] RE: Tissue fixation help

Just very curious.  Why would anybody paraffin embed after the tissue
had already been frozen? Either way gets it hard enough to cut, which is
the purpose of both procedures.


Cordially,
Charles W.  Scouten, Ph.D. 
myNeuroLab.com 
5918 Evergreen Blvd. 
St. Louis, MO 63134 
Ph: 314 522 0300 x 342
FAX  314 522 0377 
cwscouten <@t> myneurolab.com 
http://www.myneurolab.com 
 

-----Original Message-----
From: histonet-bounces <@t> lists.utsouthwestern.edu
[mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of Patsy
Ruegg
Sent: Monday, October 03, 2005 2:46 PM
To: 'C.M. van der Loos'; Histonet <@t> lists.utsouthwestern.edu
Subject: RE: [Histonet] RE: Tissue fixation help

I too have thawed tissue in rt formalin and then processed and embedded
in paraffin which good morphology and IHC results (haven't tried with
antibodies to phosphorylated sites but other IHC has been fine, it all
depends on if the samples was properly frozen in the first place)  I
tried to do this with some heart tissue which had just been placed in a
-80dc freezer with out snap freezing in OCT and it was awful, but the
frozen section was bad as well.
Patsy 


Patsy Ruegg, HT(ASCP)QIHC
IHCtech, LLC
Fitzsimmons BioScience Park
12635 Montview Blvd. Suite 216
Aurora, CO 80010
P-720-859-4060
F-720-859-4110
wk email pruegg <@t> ihctech.net
web site www.ihctech.net
 

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-----Original Message-----
From: histonet-bounces <@t> lists.utsouthwestern.edu
[mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of C.M. van
der Loos
Sent: Sunday, October 02, 2005 11:43 PM
To: Histonet <@t> lists.utsouthwestern.edu
Subject: [Histonet] RE: Tissue fixation help


   Angela,

   Long  time  ago  we thawed a  frozen  tissue  sample directly in
(room
   temp.)  NBF  (24-48 hs). Morphology was kept surprisingly well.
Sorry,
   at that time phosphorylated antibodies were not even existant....

   Chris van der Loos, PhD
   Dept. of Pathology
   Academic Medical Center M2-230
   Meibergdreef 9
   NL-1105 AZ Amsterdam
   The Netherlands

   phone:  +31 20 5665631

   Date: Fri, 30 Sep 2005 08:25:24 -0400
   From: Angela McNabola <angela.mcnabola.b <@t> bayer.com>
   Subject: [Histonet] Tissue fixation help
   To: [1]Histonet <@t> lists.utsouthwestern.edu
   Good Morning,
   Does  anybody  on  the histonet have any experience with taking
tissue
   that has
   been snap frozen in minus 80, and then "thawed" out and formalin
fixed
   and
   paraffin embedded?
   I  won't  get into the reasons why we have to do this, but does
anyone
   have a
   protocol  (or just slowly thaw it out and fix it??).  How did your
IHC
   turn out,
   especially  when  using  phosphorlyated  antibodies?  Did you get
good
   morphology of
   your tissue?
   thanks in advance!
   Angela
   Angela McNabola, MS HT(ASCP)SLS, QIHC
   Bayer Healthcare
   400 Morgan Lane
   West Haven, CT 06516
   203-812-5001
   angela.mcnabola.b <@t> bayer.com

References

   1. mailto:Histonet <@t> lists.utsouthwestern.edu
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