Perhaps I'm missing something here too. Did you decalcify the tonsil for the
same length of time as the mouse femur? If you are looking at e.g. CD markers
in bone or indeed bone marrow, it is important that you have positive control
material that you know works with undecalcified tissue and a
Just curious how often everyone is taking their cryostats down, I know cap
says every week if used daily. Thanks ahead for the info. Everyone have a
great weekend
Anita Dudley
Providence Hospital
Mobile Alabama
ANP.12087 states that the cryostat needs to be defrosted and wiped clean with a
tuberculocidal.
Can someone tell me what they use that meets the CAP criteria listed above.
thankis,
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Ann,
There are many tuberculocidal cleaners. Just search for it. If you are in a
hospital the central supply will most likely have some in stock.
We use PD-128 by Spartan Chemical
http://www.spartanchemical.com/products/product/101604
Here are some references for cryostat cleaning:
We wipe out the excess tisue( if there is any), wipe down the chamber with
abs. Alcohol then spray the chamber with CaviCide, let it sit for @ 3-5
minutes and then wipe the chamber out again.
Valerie A. Hannen, MLT(ASCP),HTL,SU(FL)
Histology Section Chief
Parrish Medical Center
951 N.
Does anyone out there have Dako IHC and special stains as well as their HE
coverslipper? We currently use Ventana and are needing an upgrade soon.
Any pros and cons would be greatly appreciated. Thanks!
B
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Hi Collen,
You had great responses to your question. I do stain mouse femurs for IHC
and IF. We fix in NBF overnight and decal for 4-5 days in 0.5M EDTA pH=8 at
room temp. After decal we wash with running tap water and re-fix for 4 hrs
with NBF. 90% of the antibodies we use on undecal tissues
I am out of the office until 08/19/2013.
I will be out of the office today. If you have a question about an order or
need assistance placing an order, or if the matter is urgent, please call
877-881-1192 between 8am and 8pm and a VWR Healthcare Service associate
will assist you. For quote
Hi Colleen,
I would say it's unusual, but not completely impossible that EDTA has
interfered with your IHC. We had that problem with demonstrating
B-galactosidase in mouse bones. If we decalcified it in EDTA after whole mount
staining in X-gal, the blue staining was removed. But if we
Hello,
There seems to be a lot of suggestions for Mallory Trichrome staining involved
in Acid fusin, Aniline blue, and orange G.
My sample of avian embryos were
fixed with Formalin based fixative (4% paraformaldehyde in
phosphate-buffered saline and 1% glutaraldehyde) overnight, in case of
10 matches
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