Gary
I think that might have to do with the fan motor inside the unit, it might need
to be replaced. We had ours replaced a few years ago. Do you service/PM the
cryostat yearly?
Liz
Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
Premier Laboratory, LLC
PO Box 18592
Boulder, CO 80308
(303) 682-394
My Leica CM 1850 cryostat is making a chirping sound and I can't figure
out what is doing this. Has anyone experienced this sound, if what was
the resolve.
Thanks
Gary
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My impression is that your problem is during the decalcification step. It
cannot be hurried and has to be in EDTA at pH 7All reagents have to be prepared
in pH7 phosphate buffer.The inconsistency resides in the fact that not all core
Bx are the same regarding thickness, tissue condition or size.
Good to know that I am not the only on that think Rene is negative to others.
Hey Rene it's not just one person that thinks your a dirt bag.
From: histonet-requ...@lists.utsouthwestern.edu
Sent: Tuesday, May 3, 2016 12:00 PM
To: histonet@lists.utsouthwe
Hello Everyone,
I am completely new to the technique, i tried several different protocols
but it doesn't seemed to succeed that very well. Does anyone have a
protocol for the Golgi Kopsch, where i have to include the tissue in the
end with paraffin?
Thank you all for your time
Mwerdler
UNAM Mex
I have been completely disappointed at the remarks and ugliness that I have
seen lately on this post. I will be extremely unlikely to continue to use this
list serve anymore due to the complete lack of professionalism and compassion
that has been displayed of late. This blog post talk has certa
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| Dear Friends & Family,I am seeking a Research Scientist I, Stem Cell Biology
for a stem cell therapy project that we just started. The funding has been
secured for the entire project. The position is available immediately and the
description is shown below. If you know somebo
We are still having issues with our PAS stain on decaled bone marrows. The
Pathologists in HemePath are seeing what they refer to as smudginess in cells
on some areas of the completed PAS slides. We have looked at everything and
cannot find where the issue is coming from at this point. We hav
My vendor (Cell Marque/Sigma Aldrich) has a YEAR backorder on this IHC RTU.
Does anyone have a vendor they purchase from that I can research? Thanks so
much.
Kari M Simeone
Histology/Immunohistochemistry Specialist Supervisor
Alternate Laboratory Supervisor
The information contained
As I see it, the best solution is "1"Even more: if the piece of tissue is large
enough,→cut 1 section and stain → select at least 2 (+) areas→ divide the block
into 2 blocks each containing one of those 2 areas and by doing so you would
have duplicated the number of possible (+) sections.René
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