I believe so, yes. This is the info I was given. Buy Biotin Antibody Rabbit
Polyclonal: A150-109A from Bethyl Laboratories, Inc. 25043 West FM 1097,
Montgomery, TX 77356, 1-800-338-9579
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
We have gotten good results with the following probes.
http://www.panomics.com/products/rna-in-situ-analysis/viewrna-ish-tissue-assay/overview
At first they were not working well but the rep come out for the day and went
over them with us and not the results are beautiful and consistent.
What detection are you using?
We only have Ventana instrumentation at our lab.
Thank you
Cecilia M. Obregon, HTL (ASCP)
Memorial Regional Hospital
3501 Johnson Street
Hollywood, FL 33021
954-265-5317
From: margaret chadwell [m_chadw...@hotmail.com]
Hi Histonetters,
I have purchased a liquid EDTA solution that is .25M. I need to make 10% EDTA.
Do I just dilute it 1/10 with DI water?
Thanks
Kimberly C. Tuttle HT (ASCP)
Pathology Biorepository and Research Core
University of Maryland
Room NBW58, UMMC
22 S. Greene St
Baltimore, MD
The MW of EDTA is 294.2. A 1M solution would therefore contain 294.2
g/L, so a .25M solution would contain 73.55 g/L. A 10% solution would
contain 100g/L, so your solution is already less concentrated than 10%.
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I sent out a request for information a while back and am going to ask again
from a different approach.
I am finding problems with embedding blocks of bone marrow particles with or
without blood clot.
Does anyone have a special technique they would like to share to concentrate
the particles
I have a question for those of you that also may perform cytology specimens at
your facility. How do you prevent carryover from one case to another? For
example, we had obvious carryover from a pleural fluid onto an FNA of a thyroid
case. This has never happened here (to our knowledge). Has
The molecular weight of the EDTA will vary depending on chemical makeup -
regardless, the solution you have is probably less than 10% already. EDTA
tri-sodium salt with MW 358 at 0.25 M is 89.5 g per liter or 8.95 g per 100 ml
or 8.95%.
-Original Message-
From:
Well you could try the warm agar approach:
Agar Cell Block Method
Reference:
Olson NJ, Gogel HK, Williams WL, et al (1986) Processing of aspiration cytology
samples: an alternative method. Acta Cytol 30:409-412.
Solutions:
1. 3% Agar
2. Fixative
Procedure:
1. Fix material in
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Don't forget EDTA doesn't fully go into solution until the pH approaches
8.0. You will need to prepare a sodium hydroxide solution for pH
adjustment.
On Wed, Jun 26, 2013 at 3:46 PM, Goins, Tresa tgo...@mt.gov wrote:
The molecular weight of the EDTA will vary depending on chemical makeup -
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