AdrienneThanks for your thoughts, however I was not in need of any study help,
having passed the exam some time ago, but was posting in response to students
questions to try to help and support them. I think your system is good if your
goal is memorization. My personal feeling is that while
Hello,
I am currently sectioning individual rat whiskers and follicles and am having
some trouble obtaining clean sections from within the centre of the whisker
(and intact bulb) without the brittle hair falling out of the block or
splintering. Does anyone know of a method that I could use to
Hello friends i wish to fine out how to use the aqueous mounting media.
thanks alot
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No harm done. I believe that you meant the Bancroft text, and it is also good
and similar in content to the Sheehan Hrapchak as well as the Pierce and Luna
publication(s) . All would suffice in my opinion, as a compliment to Carson,
it is more or less a matter of opinion and preference,
We are starting MSI testing in our lab, I am just curious if there is
any labs out there doing this on colon biopsy cases. If so we would
love some feedback. I would like to know if this is common practice
somewhere.
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Linda Wrote By the way, Histonet is coming up on its 16th year anniversary
(wow!) and there are currently 3543 members on the list (from 30 countries as
of my last tally).
That is really great. I agree with John Kiernan that Histonet really opened up
the histology community. Back in the old
Hi Everyone,
We are currently running some alk phos staining protocols with a fast red
chromogen. My pathologist would like to use something other than Hematoxylin
as a counterstain. What does everyone recommend?
Thanks,
Kim
Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA
A couple of people contacted me about a training and competency checklist for
intial, entry level HT employees. I put something together that is pretty
generic from some items I developed for a previous employer. Of course if I was
going to do this for myself, I would expand it out, but it
Us 10% aq. KOH sol. for half an ahour and process after that.
René J.
--- On Mon, 11/14/11, Adam Boanas a.boa...@epistem.co.uk wrote:
From: Adam Boanas a.boa...@epistem.co.uk
Subject: [Histonet] Whiskers
To: histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
Date: Monday,
For sure the one you bought come with the instructions.
In essence your section has to be wet (with water); add the mounting medium and
cover.
Let it dar.
René J.
--- On Mon, 11/14/11, Remedy Bi bire...@yahoo.com wrote:
From: Remedy Bi bire...@yahoo.com
Subject: [Histonet] using Aquoes
Hi All
Anyone have any recommendations for a pan cytokeratin that works in mouse
tissue?
Thanks
Luis
/PRE
html
body
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This email message, including any attachments, is for the sole use of the
intended recipient(s) and may contain
JenniferI got a linked in account and have never paid for it since 2008.I think
that you pay only if you want the enhanced page features. I think that the
checklist builder is under the lab quality management and competency materials
from CAP. I posted the link the other day by entering
Carol-
We started doing the MSI panel on all colon resections earlier this year. We
run this on the BOND system with good results.
Nancy
Dubuque, IA
Message: 5
Date: Mon, 14 Nov 2011 11:15:19 -0500
From: Freeman, Carol carol.free...@utoledo.edu
Subject: [Histonet] (no subject)
To:
nb= sp;Although I paased it when there was still a practical, I found
that read= ing ALL of the recommended texts provided me with the
information needed to= pass the exam without the need to memorize. I
esp found the BS and th= e Carson text particularly helpful and it
nb= sp;Instead of treating the whiskers, perhaps embedding the
follicles on aga= r and then processing the agar, cutting the
agar/paraffin block with a new = balde, keeping every section, you
should be okay. You can also try and cut = them at 3 microns. I would
Histonet,
*Job Title:*Lead Histotech – 2nd shift
*Department: *Laboratory
*Reports To:*Histology Supervisor
*Shifts: *3:00pm to 11:30PM Monday thru Friday
*SUMMARY*
Under the supervision of the Histology
Can't agree more. I mean, where would Joe the Toe be without the Histonet?
By the way, just read the reviews from the lecture my buddy Hector and I
gave in Cinci this year. One of the critiques stated that Hector and I are
the biggest egomaniacs this side of space. Wow, I've been called a lot
Try 1-2% Ethyl green in acetate buffer (pH4) - will give you green nuclei (of
course)
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury
Contemplating the IHC qualification and wondering if supervisors/managers can
provide feedback as to their feeling/perception of this credential, how you
feel it might effect/limit hiring for you when you review candidates? Want to
make sure that I am investing in something that will truly aid
I am the first to admit I know little to nothing about EM. I have a
researcher who read an article today that said in the method that they had
taken cells, applied them to copper EM grids and immersed them in liquid
nitrogen to fix them. Has anyone ever heard of this technique? and if you
I've been having issues with some of my tissue marking ink drying up. Is
there any solvent I can add to reconstitute it, or do I just need to get
new bottles?
--
J Emahiser
Mohs Tech
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