Re: [Histonet] Adult Mouse Skin Cryosections
How slowly are you freezing? The freezing method you describe is not
really a slow freeze and should work perfectly as a snap freezing
method. If it IS slow, then make sure the liquid nitrogen is up almost to
top of metal block but NOT over the top of the metal block. We remove
mouse skin (shaved or without much hair) and folded it into a v shape so
the hair side is on the inside of the V, and then embedded the V on edge.
The skin orientation is such - that the knife (very sharp, disposable blade
- changed frequently for skin) passes through the soft layers first, and
hair side last. If you do it the opposite direction, the layers separate
worse as the outer layer tends to get scrunched up or pushed into the
softer layers. Sectioning at -20C produced excellent 5 um thick sections
especially if the skin is inflamed.
By temperatures, which ones? And thicknesses?
At 03:07 PM 11/21/2005, you wrote:
>I'm having trouble sectioning adult mouse skin prepared for cryosections.
>The dorsal skin has been taken freshly and put into plastic dispomoulds with
>Tissue Tek O.C.T, orientated and then slowly frozen by placing on a metal
>block which is nearly submerged in liquid nitrogen. The sample freezes
>nicely with no cracks, but when it comes to sectioning on a cryostat the
>tissue tends to scrunch up and come away from the tissue tek on the fatty
>side. Shaving the skin had no effect on the outcome. I've tried lots of
>different temperatures/section thickness but no luck.
>I'm assuming the problem has something to do with the fatty layer that is
>present with the skin, but it is very difficult (if not impossible) to
>separate this from the skin. Can anyone suggest how to get nice adult skin
>cryosections, any other processing needed to be done before mounting in
>Histonet mailing list
Research Histopathology Supervisor
Veterinary Molecular Biology
Montana State University - Bozeman
PO Box 173610
Bozeman MT 59717-3610
406 994-4303 (FAX)
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