Here is our basic microtomy protocol:
BMT - 3 HEs, each has a ribbon, plus PAS, Retic, Perls
Liver bx - 3 HEs, each has a ribbon plus Retic, Trichrome, Perls,
Renal bx - 4 HEs, each has a short ribbon plus PAS, PMS, trichrome - on
slides with gloms
Breast bx - 3 HEs, each has a ribbon
Derm bx - 4
Hi,
I am an HTL(ASCP) certified Histotechnologist with many years of
experience. I am looking for a new position as IHC Specialist/IHC
Supervisor/IHC Tech.
Open to relocation.
Isaac.
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Histonet mailing list
Hi there,
HE QC should be carry out on every slides that are stained, if you are checking
for the staining intensity, this will be carried out using a control slide on
new batch of staining solution, commercial or house made. Batch number should
be recorded, and slides labelled with batch
I was wondering who out there in Histo Land is using or has used the Ventana
Symphony HE stainer and what their experiences have been. Thanks in advance!!
Kelly D. Boyd, BS, HTL (ASCP)
Lab Manager
Harris Histology Services
Tele (252)-830-6866
(800)-284-0672
Cell (252)-943-9527
Fax
We have a great full time permanent opportunity for an experienced
histotech at Abbott Laboratories in Abbott Park, IL. We are about 40 miles
north of Chicago in Lake County. Please go to www.Abbott.com if you are
interested in applying for this position. Additionally, if you would
like to
Hi - I'm cleaning out my office and found the procedure manual, timing disc
and notes for the old A/O TP8000 Processor.If for some reason someone
would like these I will mail them to you. Otherwise they are going in the
trash.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Beauty mark - like Cindy Crawford has.
Andrea Grantham, HT (ASCP)
Senior Research Specialist
University of Arizona
Cell Biology and Anatomy
Histology Service Laboratory
P.O.Box 245044
Tucson, AZ 85724
algra...@email.arizona.edu
Tel: 520.626.4415 Fax: 520.626.2097
happy slicing and
Hi all,
I've recently run into a problem troubleshooting IHC on mouse bones. I am
using the tyramide amplification system using a goat primary, anti-goat
biotin, strepavidin-HRP, biotinyl tyramide, followed by another
strepavidin-HRP and then DAB+ from Dako. When I use an isotype goat IgG, I
get
Hello,
We currently use a Benchmark Ultra and it is worth several XTs. There are some
features about it that you should know about before you start a run. What we
currently do in our lab is load all of the antibodies we are likely to run
every day. This can be troublesome if you run the
hello, will some one please give me pointers on successful methods used
for cryosectioning bursa esophagus from approx. 21 day chick embryos
(such as recommended temp. micron thickness, for yielding the best
sections)? Thanks! Atoska
___
Histonet
hello, if any of you have acetone fixation incorporated into you frozen
section H E staining protocol will you please advise me on adjustments
necessary for routine staining protocol. Also, out of curiosity please
enlighten me on the purpose for post sectioning acetone fixation on
tissue samples
It depends on your volume and how long you maintain your slides. Because you
are a children's hospital you keep them longer.
The Leica brand is very troublesome in high volume situations. I personally
prefer Sakura tape for the speed and fast drying time.
-Original Message-
From:
We've had our Sakura film coverslipper since '94 and love it. The
goodsaves us tech time coverslipping for hours each day, plus
you can file the slides right away. The bad.the docs prefer the
bone marrow smears to be coverslipped by hand. We have about 12 bone
marrows a
What is your goal? A routine HE or immuno'setc.??
Atoska Gentry gent...@auburn.edu 3/25/2010 12:21 PM
hello, if any of you have acetone fixation incorporated into you
frozen
section H E staining protocol will you please advise me on
adjustments
necessary for routine staining protocol.
Leica CV3050
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Margaryan,
Naira
Sent: Thursday, March 25, 2010 12:07 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] coverslipper
Hi Colleges,
I
hi all
i am trying to do an in situ hybridization in whole mount brains at
P7 but is hard to get staining mostly due to permeabilization issues
since is 7 days postnatal brain. I would really appreciate to receive
any suggestion or protocol to help me in this issue.
Thanks a lot in
Thanks a lot to all of you answered me. I was surprise nobody mentioned
coverslipper from DAKO. Are any of you have any experience with DAKO's
coverslipper?
Again Thanks to all,
Naira
Subject: coverslipper
Hi Colleges,
I need your opinion about coverslip by hand vs. using machine.
If you
On 3/25/10 1:04 PM, histonet-requ...@lists.utsouthwestern.edu
histonet-requ...@lists.utsouthwestern.edu wrote:
Send Histonet mailing list submissions to
histonet@lists.utsouthwestern.edu
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We use the Leica CV5030 the advantage of it is that it can be attached to
their Auto stainer providing continuous workflow as rack and coverslip 30
slides per run, without the need to physically transfer slides rack between
the autostainer and coverslipper or used as a stand alone coverslipper if
I purchased a used Hacker RCM-3660 glass coverslipper several years ago. It
was missing some parts and the nice people from Hacker supplied me with the
needed parts. This work horse has been running 7 days a week for the past
several years and has never given us any problems. Great machine and
Is this coverslipper now produced by Medite
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of jstaruk
Sent: Thursday, March 25, 2010 2:40 PM
To: malbena...@gmail.com; 'Lynette Pavelich'
Cc:
Yes. I block in 3% H2O2, followed by protein block (it's a mysterious buffer
called TNB that comes with the tyramide amplification kit), and then
avidin/biotin.
Adam
On Thu, Mar 25, 2010 at 2:25 PM, Margaryan, Naira
nmargar...@childrensmemorial.org wrote:
Hi Adam,
How do you block?
I
Hi - Got a taker for the directions. Who know?
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinary Medicine
Louisiana State University
Skip Bertman Drive
Baton Rouge, LA 70803
225-578-9734
FAX: 225-578-9720
I have some primate brain blocks to do. When I section the blocks the
sections look nice. When I put the ribbon on the water bath( temp is
47) the tissue is wrinkled around the edges. No amount of time on the
water makes this better. Ideas to solve this problem would be
appreciated.
At what thickness do you cut your sections ?
For Human brain we cut section at room temperature moist in Molifex and cut
sections at 7 µm for standard HE/ 14 µm for LFB.
Not sure what is the melting point of the wax your use, but if it is around
57 oC you can safely raise the temperature of
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