Dear histonet users,
I am just starting to do cryosections and I ran into a problem. I have mouse tissue that we freeze in OCT (we tried different tissue preprocessing: PFA immersion fix, whole animal PFA perfusion, sucrose gradient). I am sectioning skeletal muscle at 10 micron.
When I look at the sections directly after sectioning (slide is still cold)=2C the morphology looks ok. However, if I allow the slide to warm to room temp than the tissue start to 'tear' apart and the individual fibers get separated. I could keep the sections at -20C and they will be ok, however=2C during staining the slides will warm to RT and the above problem occurs.
What can I do to prevent the tissue from starting to tear?
Gerben, Rotterdam, The Netherlands
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