[Histonet] Help with cutting mouse brain at 9-10 microns

2015-02-18 Thread Coffey, Anna (NIH/NCI) [C]
Hi Kimberly,

Most of what I work with is mouse tissue and I've found the brains to be a bit 
tricky because they both hydrate and dry out quickly. I normally keep the 
paraffin blocks on an ice for about 2 hours (after they've been fully faced 
in), checking periodically to make sure the tissue is not overhydrating. When I 
section, I can normally only take a few sections before the brain starts to dry 
out again (you can tell when you start to see scratches and dry white areas on 
the tissue). Most of the blocks are ready to cut again after a few additional 
minutes back on the ice.

For thicker sections (up to 20um), I take use the wooden stick of a cotton swab 
and hold it against the base of the paraffin block as I cut the section. The 
section will curl around the stick and you can roll it out flat on the water 
bath to smooth it out.

Hope this helps!

Anna Coffey, MS, HTL(ASCP)CM
Histotechnologist
Center for Advanced Preclinical Research
Frederick National Laboratory for Cancer Research
Leidos Biomedical Research, Inc.
Bld 539, 224
Frederick, Maryland 21702
301-846-1730

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[Histonet] Help with cutting mouse brain at 9-10 Microns

2015-02-18 Thread Kimberly Marshall
?Hello Histo folks


  I am starting a research project with mouse brain,  I am having trouble with 
chatter on the regular 3.5 mm sections and cant get the 9-10 mm to cut at all.  
I have soaked them in warm water and wonder in using a  softener like 
conditioner would help.  I am new to the animal tissue world and any advise 
would help.


Thanks in advance.

Kimberly
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