Hi Histo-lovers!
I am planning on doing some nissl staining on neonatal mouse brain, to identify
the trigeminal ganglion.
Does anyone have a nissl stained atlas of mouse brain @ P0 (newborn) ?
Has anyone had experience with this before?
If so, would you mind sharing any tips?
--
Kevin
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Hi Histoneter,
I was just wondering what kind Health and Safety of procedures do people use to
monitor Chloroform Fume ?
I was carrying an HS audit for occupational exposure Xylene / Glutaraldehyde
/ Formaldehyde/ Chloroforms fumes
Message: 10
Date: Tue, 20 Apr 2010 16:56:48 -0400
From: thisis...@aol.com
Subject: [Histonet] CAP Checklist
To: histonet@lists.utsouthwestern.edu
Message-ID: 8ccaee3211e306a-1c94-1...@webmail-m053.sysops.aol.com
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Can someone tell me where on the CAP
Message: 2
Date: Tue, 20 Apr 2010 10:27:57 -0700
From: sris...@mail.holyname.org
Subject: [Histonet] (no subject)
To: histonet-boun...@lists.utsouthwestern.edu,
histonet@lists.utsouthwestern.edu
Message-ID:
of4a13f24e.175f330a-on8525770b.005f84cc-8825770b.006ff...@holyname.org
Content-Type:
Along with the new CAP/ASCO ER/PR guidelines there was a front page article in
the NY Times yesterday: Cancer Fight: Unclear Tests for New Drug. It details
the issues with interpreting Her2 staining and the continuing issue with
disparate results from different labs when doing ER, PR and Her2
Kevin,
This article has a nice photo showing mouse trigeminal ganglia. Google
images is your friend--
Mike
Nature Protocols 2, - 152 - 160 (2007)
Production of dissociated sensory neuron cultures and considerations for
their use in studying neuronal function and plasticity
Sacha A Malin,
Tony's answer (62 degrees C for 25 mins) is the minimum to ensure section
adheres to slide. We all have to stain slides that have been baked longer than
30 mins. However, especially for Her2, longer baking times can result in false
negatives or at least diminished staining. The justification
I'm in a bit of trouble. I work in the south of Brazil (Porto Alegre) for some
years and now in my hospital a lot of bone marrow biopsies are being performed
(leukemia and lymphomas). With decalcification with strong acids (nitric) I'm
getting very poor results with the immunohistochemistry.
They have commercial rapid decals that are formic acid based that do not affect
the immunohistochemistry. But it does affect some of the enzyme
histochemistry.
Loralee McMahon, HTL (ASCP)
Immunohistochemistry Supervisor
Strong Memorial Hospital
Department of Surgical Pathology
(585)
Hello all
I have a question on tape coverslips. We received a couple tape
coverslipped slides in for scanning and the tape is completely removed
from the slide. I would normally just coverslip with glass but the
tissue is on the tape coverslip and not on the slide. How can I re
attach the
Just put the slide in xylene and coverslip with the tape containing the
tissue. The you could put a couple small drops of mounting media on for
good measure.
Mike
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On
Thanks it worked
Liz
Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
Manager
Premier Laboratory, LLC
PO Box 18592
Boulder, Colorado 80308
office (303) 682-3949
fax (303) 682-9060
www.premierlab.com
Ship to Address:
1567 Skyway Drive, Unit E
Longmont, Colorado 80504
-Original Message-
Hello to all,
I was wondering if anyone knows where to purchase toluidine blue (for mast
cells) other than polyscientific.
Thank you in advance for your replies,
Jenny
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Hello,
For those of you who are ASCP certified, either HT or HTL, did many of you
have to take the exam more than once? I have not yet sat for the exam, but
I see the pass rate is low, and average score is usually just slightly above
the pass line. I have read a lot of comments on some message
Eric,
Some of my thoughts on your discussion questions:
1. How do you monitor the shortened baking time, especially when
multiple racks of slides are cut throughout the day?
We have timers set for when each rack goes into the oven. This might be
an issue for labs with larger batches (we are a
Hi,
If cost is a problem for charged slides, you could always silanize them
yourself using whatever slides you want. It takes some time, (time=money)
but the slides themselves are cheaper. There is a great description with
procedures here:
Newcomer
Claire
From: histonet-boun...@lists.utsouthwestern.edu on behalf of
zodia...@comcast.net
Sent: Wed 4/21/2010 5:35 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Toluidine blue
Hello to all,
I was wondering if anyone knows where to
Are you kidding!?! I have an AA in Histotechnology and still didn't pass my
(HTL) written on the first round. I did pass my slide review though, thank you
very much. :) I passed on the second try, which included 3 years of OJT and
tons of studying after graduating school. (BTW, I also have a
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