Re: [Histonet] help ! paraffin section

2012-08-08 Thread Rene J Buesa
What you describe is a typical example of poor paraffin infiltration = the 
paraffin has not infiltrated the tissue and when you prepare the final block it 
will consist of 2 different components; the tissue and the paraffin. That is 
why you end with a good paraffin section without the tissue.
Poor paraffin infiltration is always caused by an improper sequence while 
tissue processing. Either the fixation is incomplete 
OR the dehydration is incomplete and there is water in the tissue when you go 
to the clearing stage 
OR the clearing stage is incomplete and the tissue still has alcohol 
(immiscible with paraffin) when the tissue goes to the paraffin 
OR the paraffin infiltration is too short.
The problem resides in your processing protocol and there is nothing you can do 
about that at the end.
Try to check your processing protocol to eliminate the problem.
If this is happening all of the sudden while you used to have good results 
previously, then you either have changed reagents or the reagents are not in a 
good condition.
René J. 



From: Megha Kumar meg...@g.clemson.edu
To: histonet@lists.utsouthwestern.edu 
Sent: Tuesday, August 7, 2012 11:45 PM
Subject: [Histonet] help ! paraffin section

Hi All
I am trying to section adult mouse intestine and skin using paraffin
embedding. However, when i section, the tissue is torn although the rest of
the paraffin looks perfect. Please suggest why this is happening. Also,
sometimes the skin sections fall off the slides when I perform in situ
hybridization. Any ideas how to prevent this?
Please help! i am a beginner in histology and dont' know what to do!
regards
Megha


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Re: [Histonet] help ! paraffin section

2012-08-08 Thread Mehmet Fatih BOZKURT
In addition to Rene's comment,to cut coagulated tissue (skin that have
new wound crust) and calcified tissue is difficult.

On Wed, Aug 8, 2012 at 6:45 AM, Megha Kumar meg...@g.clemson.edu wrote:

 Hi All
 I am trying to section adult mouse intestine and skin using paraffin
 embedding. However, when i section, the tissue is torn although the rest of
 the paraffin looks perfect. Please suggest why this is happening. Also,
 sometimes the skin sections fall off the slides when I perform in situ
 hybridization. Any ideas how to prevent this?
 Please help! i am a beginner in histology and dont' know what to do!
 regards
 Megha


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 Histonet@lists.utsouthwestern.edu
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-- 
Mehmet Fatih BOZKURT, DVM, PhD
Afyon Kocatepe University
Faculty of Veterinary Medicine
Department of Pathology
03030, ANS Campus
Afyonkarahisar-TURKEY
Tel: +902722281312-173/237
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