[Histonet] Re: chemicals that are made in the lab

2011-03-23 Thread Nathan Jentsch
Michele,
I would use the expiration dates from the original alcohol bottles for
graded alcohols.  Alcohol won't expire any faster just because you dilute
it.  I use two years from the month of recycling for an expiration date for
recycled product.  In reality these chemicals won't expire for decades as
long as they're not contaminated, but a state inspector will want to see
reasonable numbers, and I know we will use the chemicals long before the two
year mark hits.
Nathan Jentsch
BS HT(ASCP)
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Re: [Histonet] B5

2011-03-23 Thread Lee & Peggy Wenk
We switched a few years ago. Hospital went mercury free, and we couldn't 
find any company in 6 states that would take waste mercury.


One common mistake when converting to a zinc formalin is to try to fix it 
the same time as the B5. Mercury binds/fixes very quickly, zinc is slower. 
It's chemistry, and there's not much you can do to make it go a whole lot 
faster. So, whatever time you fixed normally in B5, multiply it by 1.5 to 
2.0 (2 hour B5 fix will now require 3-4 hours fixation in a Zinc formalin). 
If you don't fix long enough in the zinc formalin, the tissue is going to 
have smudgy pale blue nuclei on the bone marrow. Been there, done that when 
one of the med techs insisted on fixing in the zinc formalin for the same 2 
hours as B5 because she didn't like her routine disrupted (B5 was 2 hours, 
so she insisted the zinc formalin should also be 2 hours). Once we showed 
her the difference in quality between 2 hours and 3 hours, and asked her 
which one she would like her daughter's bone marrow biopsy to look like, if 
we ever had to diagnose her for leukemia, she changed to 3 hours, and now 
the bone marrows look fine.


Peggy A. Wenk, HTL(ASCP)SLS
Beaumont Hospital
Royal Oak, MI 478073

--
From: "Pitts, Jaclyn S. (Jackie), HT(ASCP)" 
Sent: Tuesday, March 22, 2011 9:45 PM
To: 
Subject: [Histonet] B5


Hey all,
I was just curious how many of you out there still use B5 as a fixative
for bone marrows.
Thank

Jaclyn Pitts, HT(ASCP)
Histotechnician
Department of Laboratory Medicine and Pathology
Mayo Clinic Rochester, MN
E-mail: pitts.jac...@mayo.edu



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[Histonet] Re: Verhoeff/Masson's Stain

2011-03-23 Thread Robert Richmond
The comments on Verhoeff's hematoxylin should be sufficient to
trouble-shoot this cumbersome but beautiful old stain - I don't know a
stain I'd rather photograph, except maybe Ramón y Cajal's gold
sublimate.

Verhoeff's hematoxylin is a century old this year. The original paper
is in the JAMA, of all places - I think I had a photocopy once. (We
need a commemorative postage stamp!)

Frederick Herman Verhoeff (a.k.a. Freddy, 1874-1968 - I've always
heard it pronounced veer-hoff) was the founder of American
ophthalmologic pathology. Working solo in a little lab at the
Massachusetts Eye and Ear Infirmary, he published a great number of
papers in ophthalmology. He intended his stain to demonstrate myelin
sheaths in human autopsy optic nerve. It was in routine use for this
purpose at the Wilmer Eye Institute at Johns Hopkins when I was a
pathology resident there in the later 1960's, when Dick Green (died
last year at 76) was the chief of eye pathology.

Bob Richmond
Samurai Pathologist
Knoxville TN

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RE: [Histonet] RE: B5

2011-03-23 Thread Pitts, Jaclyn S. (Jackie), HT(ASCP)

 Thanks. I am not sure who disposes of the B5 for us but I do know that
it would be much easier if we changed to something else. 


Jaclyn Pitts, HT(ASCP)
Histotechnician
Department of Laboratory Medicine and Pathology
Mayo Clinic
E-mail: pitts.jac...@mayo.edu

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
jeffery.mil...@spectrum-health.org
Sent: Wednesday, March 23, 2011 7:56 AM
To: Pitts, Jaclyn S. (Jackie), HT(ASCP);
histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: B5 

We did until about 7 yrs ago when the hospital decided that all mercury
(thermometers and chemicals) would no longer be allowed which was fine
with us. We just went to 10% NBF since then.


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Pitts,
Jaclyn S. (Jackie), HT(ASCP)
Sent: Tuesday, March 22, 2011 9:46 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] B5 

Hey all, 
I was just curious how many of you out there still use B5 as a fixative
for bone marrows. 
Thank

Jaclyn Pitts, HT(ASCP)
Histotechnician 
Department of Laboratory Medicine and Pathology
Mayo Clinic Rochester, MN 
E-mail: pitts.jac...@mayo.edu



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[Histonet] RE: Stupid Rabbit Primary Antibodies

2011-03-23 Thread Goins, Tresa
You might try Background Sniper from Biocare or Background Buster from Innovex 
- we process animal tissues exclusively and we use several rabbit primary 
antibodies.


Tresa Goins, Ph.D.
Histopathology Supervisor
Department of Livestock
Bozeman, Montana



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
sgoe...@mirnarx.com
Sent: Tuesday, March 22, 2011 3:04 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Stupid Rabbit primaries!

So I haven't had to deal with rabbit polyclonal primaries in a long time
because I remember how much the background sucks with them.
Unfortunately the only available antibody is a rabbit polyclonal.  Does
anyone have any suggestions for how to eliminate the background?  I have
diluted almost to the point of the antigens not showing!  Thanks guys
and gals!!

 

Sarah Goebel, BA, HT(ASCP)

Histotechnologist

Mirna Therapeutics

2150 Woodward Street

Suite 100

Austin, Texas  78744

(512)901-0900 ext. 6912

 

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RE: [Histonet] Underfixation of breast tissue may lead to falseresults?

2011-03-23 Thread Troyer, Dean A.
Just wanted to qualify somewhat the observation that alcohol is a poor 
fixative.  Alcohol can be very effective as a primary fixative.  
 
I agree formalin isn't likely to be displaced in this country soon, but aqueous 
ethanol or methanol is a viable alternative that has merits worth considering. 
 
Dean Troyer
Eastern Virginia Medical School



From: histonet-boun...@lists.utsouthwestern.edu on behalf of Bryan Llewellyn
Sent: Wed 3/23/2011 1:28 PM
To: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Underfixation of breast tissue may lead to falseresults?



This has been commented on several times by old fogey histotechs in the
past.

Any formalin variant takes some time to actually chemically alter (fix)
the tissue.  Usually this is a minimum of 24 hours for a 3-4 mm thick
piece.  In modern labs there is a focus on 24 hour or less turnaround
time, so formalin fixation is usually minimalist and may be inadequate,
as in this case.  After all, the universe will not change itself for our
benefit just because we want fast results.

This means that underfixed tissues with just a few hours in formalin are
processed.  The unfixed components are exposed to ethanol during this
process.  Remember that ethanol is also a (very poor) fixing agent, so
the inadequatly fixed tissue is fixed by it, with all the
characteristics ethanol fixation gives, shattering, hardening,
distortion, etc. This is frequently referred to as "overprocessing", but
it is just poor fixation from ethanol. For most tissues, wetting the
block surface allows reasonable sections to be cut, but that is only a
quick fix.

Procedures which require tissues to be properly fixed may not be
successful as a consequence.

Bryan Llewellyn


Goodwin, Diana wrote:
> Dear Histonetters:
>
> I recently read the following in an article on Medscape:
>
> "Underfixation of breast tissue may lead to false negative ER results and 
> false-positive HER2 results.  In these situations, the tissue is actually 
> fixed in 100% ethanol, which is used to dehydrate the specimens after 
> fixation."
>
> Can anyone explain?
>
> Diana Goodwin
> Supervisor, Histology Laboratory
> xt. 6996
>
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Re: [Histonet] Underfixation of breast tissue may lead to false results?

2011-03-23 Thread Bryan Llewellyn
This has been commented on several times by old fogey histotechs in the 
past.


Any formalin variant takes some time to actually chemically alter (fix) 
the tissue.  Usually this is a minimum of 24 hours for a 3-4 mm thick 
piece.  In modern labs there is a focus on 24 hour or less turnaround 
time, so formalin fixation is usually minimalist and may be inadequate, 
as in this case.  After all, the universe will not change itself for our 
benefit just because we want fast results.


This means that underfixed tissues with just a few hours in formalin are 
processed.  The unfixed components are exposed to ethanol during this 
process.  Remember that ethanol is also a (very poor) fixing agent, so 
the inadequatly fixed tissue is fixed by it, with all the 
characteristics ethanol fixation gives, shattering, hardening, 
distortion, etc. This is frequently referred to as "overprocessing", but 
it is just poor fixation from ethanol. For most tissues, wetting the 
block surface allows reasonable sections to be cut, but that is only a 
quick fix.


Procedures which require tissues to be properly fixed may not be 
successful as a consequence.


Bryan Llewellyn


Goodwin, Diana wrote:

Dear Histonetters:

I recently read the following in an article on Medscape:

"Underfixation of breast tissue may lead to false negative ER results and 
false-positive HER2 results.  In these situations, the tissue is actually fixed in 100% 
ethanol, which is used to dehydrate the specimens after fixation."

Can anyone explain?

Diana Goodwin
Supervisor, Histology Laboratory
xt. 6996

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[Histonet] RELIA Histology Careers Bulletin 3/23/2011 March Madness is Here!!

2011-03-23 Thread Pam Barker
Hi Histonetters!
I hope you had a fun and lucky St. Patricks Day.   
March Madness has started and in addition to some great College
Basketball.  I have been experiencing the madness as well.  My phone has
literally been ringing off the hook with some great new opportunities.
All of these positions are permanent full time positions and my clients
offer excellent compensation, benefits and relocation assistance.  Best
of all these clients are motivated to hire and eager to meet you!
 
Here is a list of my current openings:
 
HISTOLOGY/PATHOLOGY  MANAGEMENT
ME – Portland Histology Lab Supervisor (Night shift)
NC – Asheville Histology Lab Manager
FL – Sarasota Histology Supervisor/Lead Tech
CA – Modesto – Histology Lab Manager
NH – Manchester Cytology/Histology Supervisor
LA – Baton Rouge Early Morning Histology Supervisor
 
HISTOTECHS
NC – Charlotte Mohs Histotech
TX – Dallas Night Shift Histotech
TX – Tyler Dermpath Histotech – New grads welcome!
LA – Lafayette Night Shift Lead Tech
OR – Portland Night Shift Histotech
MA – Cape Cod Histotech
MA – Peabody Night Shift Histotech
FL – Fort Myers  Mohs Histotech
FL – Sarasota Dermpath histotech
 
If you or anyone you know might be interested in any of these positions
or want help with a job search in another area please contact me.  I can
be reached at 866-607-3542 or rel...@earthlink.net.
 
Thank You!
 
Pam Barker
President
RELIA Solutions
Specialists in Allied Healthcare Recruiting
5703 Red Bug Lake Road #330
Winter Springs, FL 32708-4969
Phone: (407)657-2027
Cell: (407)353-5070
Toll Free: (866)607-3542
FAX: (407)678-2788
E-mail: rel...@earthlink.net 
www.facebook.com  search Pam Barker RELIA
www.linkedin.com/reliasolutions
www.myspace.com/pamatrelia
www.twitter.com/pamatrelia
 
 

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RE: [Histonet] B5

2011-03-23 Thread Weems, Joyce
Who do you get to discard it? Do you pay a fortune? j 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Laurie Colbert
Sent: Wednesday, March 23, 2011 10:23
To: Pitts, Jaclyn S. (Jackie), HT(ASCP); histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] B5 

We do! Our pathologists aren't interested in using any other fixative.
Laurie Colbert

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Pitts, Jaclyn 
S. (Jackie), HT(ASCP)
Sent: Tuesday, March 22, 2011 6:46 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] B5 

Hey all,
I was just curious how many of you out there still use B5 as a fixative for 
bone marrows. 
Thank

Jaclyn Pitts, HT(ASCP)
Histotechnician
Department of Laboratory Medicine and Pathology Mayo Clinic Rochester, MN
E-mail: pitts.jac...@mayo.edu



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RE: [Histonet] B5

2011-03-23 Thread Laurie Colbert
We do! Our pathologists aren't interested in using any other fixative.
Laurie Colbert

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Pitts,
Jaclyn S. (Jackie), HT(ASCP)
Sent: Tuesday, March 22, 2011 6:46 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] B5 

Hey all, 
I was just curious how many of you out there still use B5 as a fixative
for bone marrows. 
Thank

Jaclyn Pitts, HT(ASCP)
Histotechnician 
Department of Laboratory Medicine and Pathology
Mayo Clinic Rochester, MN 
E-mail: pitts.jac...@mayo.edu



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[Histonet] Underfixation of breast tissue may lead to false results?

2011-03-23 Thread Goodwin, Diana
Dear Histonetters:

I recently read the following in an article on Medscape:

"Underfixation of breast tissue may lead to false negative ER results and 
false-positive HER2 results.  In these situations, the tissue is actually fixed 
in 100% ethanol, which is used to dehydrate the specimens after fixation."

Can anyone explain?

Diana Goodwin
Supervisor, Histology Laboratory
xt. 6996

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[Histonet] Re: vytec formalin neutralizer

2011-03-23 Thread Matthew Lunetta
Nirmala
We Use Vytec and after consulting with the city's public utility it is ok for 
us to dispose of the waste with copious amounts of water down the drain. So, I 
would contact you local water authority and see if you can do the same. 
Regards,
Matt Lunetta BS HT(ASCP)cm
Longmont United Hospital
Longmont, Colorado



Message: 4
Date: Tue, 22 Mar 2011 10:33:12 -0700
From: sris...@mail.holyname.org
Subject: [Histonet] vytec formalin neutralizer
To: histonet-boun...@lists.utsouthwestern.edu,

Message-ID:


Content-Type: text/plain; charset="US-ASCII"

Hi Everyone,

Is there any one out there who is neutralizing the 10% formalin with 
Vytec neutralizer? How are you disposing the formalin after 
neutralization? Need some information regarding this.

Thanks in advance

Nirmala
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Re: [Histonet] please remove me from list. Thank you.

2011-03-23 Thread Emily Sours
No.

And you're not welcome.

It has become almost a cliche to remark that nobody boasts of ignorance of
literature, but it is socially acceptable to boast ignorance of science and
proudly claim incompetence in mathematics.
-Richard Dawkins



On Tue, Mar 22, 2011 at 9:34 PM,  wrote:

>
>
> Please remove me from list. Thank you.
> Dannie Blake
>
>
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RE: [Histonet] Ventilated Specimen Storage

2011-03-23 Thread Gill, Caula A.
We have one in our gross room.
Caula Gill(HT)ASCP
 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Amy Self
Sent: Tuesday, March 22, 2011 11:35 AM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] Ventilated Specimen Storage

Hello Histonetters,

How many of you have ventilated storage cabinets for storage of
specimens?

Thanks in advance for all your help,

Amy
GHS
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[Histonet] Pax 2

2011-03-23 Thread aobrien88


Is anyone using the Pax 2 antibody?  Who is your vendor and could you share 
some information about your procedure? 



Thank you, 

Andrea O'Brien 

UroPartners 
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[Histonet] RE: B5

2011-03-23 Thread Jeffery.Miller
We did until about 7 yrs ago when the hospital decided that all mercury 
(thermometers and chemicals) would no longer be allowed which was fine with us. 
We just went to 10% NBF since then.


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Pitts, Jaclyn 
S. (Jackie), HT(ASCP)
Sent: Tuesday, March 22, 2011 9:46 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] B5 

Hey all, 
I was just curious how many of you out there still use B5 as a fixative
for bone marrows. 
Thank

Jaclyn Pitts, HT(ASCP)
Histotechnician 
Department of Laboratory Medicine and Pathology
Mayo Clinic Rochester, MN 
E-mail: pitts.jac...@mayo.edu



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RE: [Histonet] B5

2011-03-23 Thread Rathborne, Toni
We do not.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu]On Behalf Of Pitts,
Jaclyn S. (Jackie), HT(ASCP)
Sent: Tuesday, March 22, 2011 9:46 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] B5 


Hey all, 
I was just curious how many of you out there still use B5 as a fixative
for bone marrows. 
Thank

Jaclyn Pitts, HT(ASCP)
Histotechnician 
Department of Laboratory Medicine and Pathology
Mayo Clinic Rochester, MN 
E-mail: pitts.jac...@mayo.edu



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[Histonet] Rabbit Anti-NeuN

2011-03-23 Thread Sohail Ejaz
Dear All 
I am looking for Rabbit Anti- NeuN antiboy to use it with anti-mouse OX42 for 
double immuno staining.
Is there any one who have used any Rabbit Anti- NeuN?
Please let me know.
Thanks
Sohail




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RE: [Histonet] Stupid Rabbit primaries!

2011-03-23 Thread Margaret Blount
Having read all the other comments, here's my 2.5 pence worth! Have you
tried a background reducing antibody diluent? You can get these from
DAKO or Menarini Diagnostics:
http://www.dako.com/uk/ar38/p107410/prod_products.htm.

Or MP-905-25 / MP-905-100, depending on the volume you require, from
Menarini Diagnostics, website
http://www.dako.com/uk/ar38/p107410/prod_products.htm.

I found these useful for rabbit polyclonals.

Good luck

Margaret

Miss Margaret Blount
Histology Manager
Metabolic Research Laboratories
Level 4 Institute of Metabolic Science
Box 289, Addenbrooke's Hospital
Hills Road, Cambridge, CB2 0QQ

Tel 01223 769061/336079

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
sgoe...@mirnarx.com
Sent: 22 March 2011 21:04
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Stupid Rabbit primaries!

So I haven't had to deal with rabbit polyclonal primaries in a long time
because I remember how much the background sucks with them.
Unfortunately the only available antibody is a rabbit polyclonal.  Does
anyone have any suggestions for how to eliminate the background?  I have
diluted almost to the point of the antigens not showing!  Thanks guys
and gals!!

 

Sarah Goebel, BA, HT(ASCP)

Histotechnologist

Mirna Therapeutics

2150 Woodward Street

Suite 100

Austin, Texas  78744

(512)901-0900 ext. 6912

 

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