Does anyone have a current protocol for Factor X111a on the Ventana Ultra
that is working for you? I would appreciate any info or support you could
give. We are using the AC-1A1 clone from Cell Marque for derms. Thanks!
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Could any Sunquest CoPath sales rep please contact me privately off the
list?
Thanks,
Drew Meyer
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I've been asked to get pricing for possible purchase of a good used/refurbished
Leica autostainer XL.
Gale Limron CT, HT (ASCP)
Histology Supervisor
This e-mail is intended only for the person or entity to which it is addressed
and may contain information that is privileged, confidential or
Does anyone know if you can just deparaffinize slides in the stainer.
Im just wondering if I also need a small stain line to dewax specials.
Thank you,
Nicole
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You can set up a just depar run.
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- Reply message -
From: Nicole Tatum nic...@dlcjax.com
To: histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
Subject: [Histonet] Leica autostainer XL
Date: Wed, Jan 26, 2011 9:48 am
Does anyone know if you can
Hi,
We run FactorX111a clone AC-1A1 on the Ultra, here is our protocol:
1. De-paraffinazation (selected)
2. Cell conditioning #1 20 minutes, then 36 minutes.
3. Antibody for 24 minutes
4. Ultra wash (selected)
5. Hematoxylin 4 minutes
6. Bluing 4 minutes.
Hope this helps.
Lisa V.
Children's
Happy hump day!
Does anyone have a good procedure for Oil Red O for FS on Muscle.
The procedure the lab I am working with is having a great deal of
problems with their muscle biopsy panel. I am trouble-shooting some
of the issues for the 1-Step Trichrome 3.4 pH, NADH, AT Pase, I am
Hi,
We use Oil Red O - but we don't do it on muscle. Our protocol is we filter the
whole bottle before we use it and then we apply it to unfixed slides for about
30 minutes. Rinse in tap water, counterstain with Hematoxylin and coverslip
with Aquamount. We use it for cytospins and occasionally
Allison
We make up our Oil Red O from scratch same day we use it, let it stand 10
minutes, and then filter with a Millipore Stericup 0.22µm, GP Express Plus
Membrane, 250ml Receiver Bottle, catalog number: SCGPU02RE under vacuum. That
seems to help a bit with the background and we are working
I have a run set up to bake the slides run them down to water ( for my
specials), another just to start at hematoxylin down to xylene etc. The
stainer allows for nearly any custom program you can think of. :o)
If you have any questions about how to set the program up, please let me know
I
I've done many of these stains and I get my ORO stain from Poly Scientific.
Actually I use the whole kit and I use Freida's protocol in the second edition.
That includes fixing in 37% formaldehyde. I filter the ORO just before use and
usually get nice clean slides. If there is a residue it
Certified Histotech needed in Santa Rosa, CA.
Part-time (25-30 hrs/wk) opportunity for an experienced and certified tech to
work in a brand new GI path lab. Competitive pay and wonderful working
environment. Send resumes to tja...@yahoo.com.
Kind Regards,
Timothy Jay
Pillar Consulting, LLC
Hello
I am looking for suggestions on the best chemical cleaner for glassware
that is used for special stains. Any ideas?
Thanks,
Nacaela Johnson
Histology Technician
KCCC Pathology
12000 110th St., Ste. 400
Overland Park, KS 66210
Office: 913-234-0576
Fax: 913-433-7639
Email:
Hello
I am really new to the field of histlogy. I wanted to get some opinions on
this
field vs. cytology. I am wondering which field is better for me. Any
suggestions
or thoughts are welcome. Thanks!!!
I remain yours truely,
Candice Camille
~ 90 mL 70% EtOH
~ 10 mL 25% HCl
Removed everything I ever had to deal with.
After that give your glassware a good wash in the dishwasher, then rinse
with plenty of demineralized water.
And wear protective gloves, but as we all do, I actually don't have to
remind any of the list members, right?
Go for HISTOLOGY!! Cytology requires a lot of Sitting in One Place
Staring into a Microscope (please! - no offense to cytotechs - really!).
With histology, your daily routine is varied and invigorating. And now
I'm probably on some Cytology Tech Blacklist... sigh...
Is there a chance to go and see a lab which does histology?
Hello
I am really new to the field of histlogy. I wanted to get some opinions on
this
field vs. cytology. I am wondering which field is better for me. Any
suggestions
or thoughts are welcome. Thanks!!!
I remain yours
Yes, I just started working in a histology lab. Thats y I was asking this
question. I heard about cytology and wanted to get some opinions as to who
offered what! Just trying to keep the options open. I doubt you are on any
blacklist. LOL!!
I remain yours truely,
Candice Camille
HISTOLOGY
UNIVERSAL WASHING INSTRUCTIONS FOR GLASSWARE
Alternative to Acid Cleaning Glassware
5% Clorox is a very inexpensive and readily available chemical
treatment solution, which is an alternative to acid cleaning. All
glassware used for special stains MUST be cleaned in the
Of course as most of us would say...histology rocks!! Most histotechs
also do cytology is most hospital settings. The only difference is that
cytotechs actually have to screen the slides that the histo people
prepare. I think that cytologists make slightly more money...but
histology is way more
Back in the day when I was trying to decide which school to pick for my
scholarship monies, I had a choice of the Med Tech program, the Cytology
program or the Histotechnology program. I had absolutely no idea what
Histology was but that is the program I choose. One of the best decisions I
ever
I just sort of fell into Histology some 40 plus years ago and never looked
back. I have left the field and always come back to it. I have done research
and clinical and still love it.
Pam Marcum
UAMS
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-Original Message-
From:
Hi histonetters,
I need suggestion and help with the TGFβ RII (D-2): sc-17799 Ab, which should
show a cytoplasmic staining. My problem is that I am getting a beautiful
nuclear staining only. How I can fix this problem? What to pay attention on and
what to change in the usual protocol? My AR is
Hello everyone,
I am working on a protocol for a dual fluorescent stain with two mouse
antibodies (one is IgG1 and the other is IgG2a). We started by
performing the two stains sequentially with a serum free protein
blocking step in between, tagging one antibody with a 488 FITC labeled
24 matches
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