Hi All
Thanks for the correction Dr Richmond. It is Hama Beads.
We keep ours in used rectangular cover slip boxes, which hold many beads of
individual colours in each box. When in use each embedder has their allocated
box at the back of the embedding centre, close to the dispensing spout, so th
I've never seen beads used for identifying individual embedders by
marking blocks with the beads. I never heard of Hama Beads (that's how
it's spelled), which I think may be called Perler Beads in the US, but
I never heard of them either. I think you can get them from Amazon.
Bob Richmond
Samurai
http://apartment-in-jerusalem.com/ngler.html
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I have done the same thing with acetone instead of alcohol...
Sarah Goebel-Dysart, BA, HT(ASCP), QIHC (ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
One place I was at didnt get many muscle biopsies so we didnt keep liquid
nitrogen and isopentane, which is what I was trained to use initially. Here's
what we did when we got a muscle biopsy and it worked fine.
After cutting the biopsy into 3-4 mm portions, we wrapped it in aluminum foil
and
Another plus for barcoding and going paperless. Scanning the cassette logs who
embedded the tissue and you can see what type of tissue it was, how many pieces
should have been there and if there were any instructions such as on end or on
edge.
Victor
Victor Tobias HT(ASCP)
Clinical Application
I called on a lab in Las Vegas when I had my sales job that used sequins. Well,
it was Vegas!
Andrea Grantham, HT (ASCP)
Senior Research Specialist
University of Arizona
Cellular and Molecular Medicine
Histology Service Laboratory
P.O.Box 245044
Tucson, AZ 85724
algra...@email.arizona.edu
I have sympathy for your dilemma!
While I have no experience with the procedure in question there have
been many, many publications since the 1960's trying to address this issue.
Personally, I have never seen one I though was much good/worth the
effort so I have just stayed with toluidine blue i
Ian,
Check with Children's Hospital in Cincinnati. The Pathology Department there
performs a lot of muscle biopsy procedures and gets a lot of outside biopsies
as well.
Bea
Beatrice DeBrosse-Serra HT(ASCP)QIHC
Isis Pharmaceuticals
Antisense Drug Discovery
2855 Gazelle Ct.
Carlsbad, CA 92010
Hi Again Gayle,
I'm sorry I was not very clear; I have already downloaded and read the
publication, and I am trying the procedure out today. I was wondering
about using a couple of substitutions and thought I might ask if
anyone has tried this procedure before.
I am on a four-week research projec
We use squares of colored construction paper. Each tech is assigned a color
and they use those or their initials for all of the different jobs in the
lab.
There has to be accountability for every job.
Jen Campbell
On Mon, Jun 25, 2012 at 9:43 AM, Amber McKenzie <
amber.mcken...@gastrodocs.net> w
Does this slow the embedder down any having to pick a bead up each time to
embed along with the tissue? I've never heard of this procedure before. The
labs I've worked in have an embedding log and we initial each case we embed.
What do you keep the beads in and are they set in a particular spo
My apologies Gayle, I am new at this...
>From Histochemistry (1994) 101:51-55, "Polychromatic staining of epoxy
semithin sections: a new and simple method," by Tolivia, Navarro and
Tolivia. I am wondering if anyone out there has tried this technique.
Thank you for your time in responding!
--Shan
Morning all,
I am taking over some work on tendon tissue and would like some advice
regarding processing schedules. The tissue is 3-5mm thick cross sections
from large tendons and is formalin fixed, paraffin wax embedded. At the
moment the sections (although flat and wrinkle free) appear cracke
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