Dear All,

There have been numerous posts  and replies over time regarding the quality 
of processed tissues, with under or over dehydration, fixation or processing 
being cited as the cause. I would lke some clarification and correction on 
my personal viewpoints on  this issue  as the case may be.

To my understanding:
a) Fixation and dehydration have an absolute end result, ie one cannot 
"over" dehydrate, as once the water is gone, it's gone. However, residual 
water is immiscible with clearing agents or wax, and would thus produce a 
soft poorly processed tissue. Thus "under" dehydration is a real entity. 
However, anecdotal evidence has stated that these tissues may become 
'alcohol-fixed" thus making them difficult to cut. What is the rationale 
behind this?

b) "Over" processing, is the result of excessive or prolonged heat 
coagulating proteins rendering the tissue into hard nasty uncuttable little 
nodules. I seem to recall this demonstrated in cookery class where eggs were 
fried to extinction and thus became an indigestible mass (there are many 
proceses and regents used in histology that bear resemblance to cooking 
school)

I realise that this might be an oversimplified version of the real 
processes, but I am interested in what the experts have to say.

Best regards

Louise Renton
Bone Research Unit
MRC
Johannesburg
South Africa
Tel & fax +27 11 717 2298
"Time flies like an arrow, fruit flies like a banana"



----Original Message Follows----
From: " Katri Tuomala" 
To: "Kelly Salceies" 
,
Subject: Re: [Histonet] Paraffin Embedding of Mice Tissue
Date: Mon, 29 Sep 2003 20:03:35 -0400

Hi Kelly,

What is your fixative for these mice tissues and how long? How big (read
thick) are your sections to be processed?
These two things will determine your routine processing protocol.
I'm not familiar with microwave processing, so I won't comment on that.
If the tissue is well fixed, there really isn't a chance to "over process"
it. The problems arise with inadequate fixation, which then leads to
alcohols and xylene drying out the tissue, and hot paraffin then causes
further damage.
Just something to think about....

Katri

Katri Tuomala
Anatomic Pathology
St.Joseph's Health Care
Hamilton, Ontaorio, Canada


----- Original Message -----
From: "Kelly Salceies" 
To: 
Sent: Monday, September 29, 2003 10:01 AM
Subject: [Histonet] Paraffin Embedding of Mice Tissue


 > Hi Everyone,
 >
 > I am a brand new Tech and am having trouble preping some mouse tissue
 > for paraffin embedding. I have all different tissues (liver, heart,
 > quads, brain, lung, and gastroc) and would like to prep all tissues (if
 > possible)  under the same conditions. I have been using the Shandon
 > Hypercenter XP or the Shandon Histowave (microwave tissue processor...).
 > Does anybody have a good protocol for mouse tissues on either of these
 > instruments?? I have tried a number of protocols, but all my tissue has
 > been really dry in cutting...
 >
 > Any suggestions would be greatly appreciated!!
 >
 >
 > Thanks,
 >
 > Kelly Salceies
 > University of New Mexico
 > Health Sciences Center
 > Dept. of Pathology
 >
 > _______________________________________________
 > Histonet mailing list
 > Histonet@lists.utsouthwestern.edu
 > http://lists.utsouthwestern.edu/mailman/listinfo/histonet



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