[Histonet] RE: Recommendations for decal solution

2010-10-25 Thread Baldridge, Lee Ann
5% Formic Acid
Thanks
Lee Ann

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Lewis, Patrick
Sent: Friday, October 22, 2010 4:06 PM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] Recommendations for decal solution

Hi guys,

 

Can anyone recommend a good decal solution.  I have some bone marrow and
trachea tissues for paraffin sectioning and I want to decal them. 

Thanks

Patrick

 

 

Patrick Lewis

Research Associate II-Bench| Infections and Prematurity

Seattle Children's Research Institute

206-884-1115  OFFICE 

000-000-  PAGER

000-000-  CELL 

206-884-7311  FAX

patrick.le...@seattlechildrens.org

OFFICE  1900 9th Avenue Seattle, WA 98101

MAIL  M/S C9S-8, Seattle, WA 98101

WWW seattlechildrens.org http://seattlechildrens.org/ 

 



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[Histonet] Great position for an HT in Nashville, TN

2010-10-25 Thread Hale, Meredith
 

Great opportunity for a Histotechnician in a brand new laboratory!
Bellmeade Dermatology in Nashville, TN is looking for a certified HT or
HTL to run their newly constructed laboratory. Bellmeade Dermatology has
been in the dermatology business for 18 years with 3 physicians and 2
Nurse Practitioners' . Candidate must be ASCP certified and CLIA
certified to perform gross dissection, prior supervisory experience
preferred. The candidate will be responsible for the following: Creation
and maintenance of policies and procedures to CLIA standards, leading
lab through CLIA inspection, maintenance and quality control for
equipment, and routine histology duties. This is a part time  position
that offers a competitive salary and  the flexible hours allows you to
put your own personal stamp on the laboratory .  Interested applicants
should contact Meredith Hale phone 214-596-2219 or through email
mh...@carisls.com

 

 

Meredith Hale HT (ASCP) CM

Operations Liaison Director and Education Coordinator 

 

Caris Life Sciences

6655 North MacArthur Blvd, Irving Texas 75039

direct: 214-596-2219

cell: 469-648-8253

fax: 972-929-9966

mh...@carisls.com 

 

 

 

 

 

 

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RE: [Histonet] Wear gloves when handling / cutting paraffin blocks.

2010-10-25 Thread Bernice Frederick
We wear gloves we have to sterile section blocks for DNA/RNA extraction.
Keeps the slides free from contamination if we are placing sections on
slides, otherwise we are sticking them in a vial. All equipment associated
with the sterile sectioning is cleaned between each block (block holder,
blade holder, forceps etc) and gloves are changed.
Bernice


Bernice Frederick HTL (ASCP)
Northwestern University
Pathology Core Facility
ECOGPCO-RL 
710 N Fairbanks Court
Olson 8-421
Chicago,IL 60611
312-503-3723


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
tahs...@brain.net.pk
Sent: Saturday, October 23, 2010 8:26 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Wear gloves when handling / cutting paraffin blocks.

Dear All,
I am looking some kind of references out there that addresses that it is
not a requirement to wear gloves when handling / cutting paraffin blocks.
Any help would be greatly appreciated
Thank in advance,
Muhammad Tahseen
Senior Supervisor
Histology
SKMCHRC
Pakistan


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[Histonet] paraffin block mailers

2010-10-25 Thread Bartlett, Jeanine (CDC/OID/NCZVED)
Hi everyone,

Does anyone know of a source for packaging exclusive to mailing paraffin
blocks?  Vendors please feel free to reply as well.

Thanks!

Jeanine Bartlett, BS, HT(ASCP)QIHC
Centers for Disease Control and Prevention
Infectious Diseases Pathology Branch
1600 Clifton Road, MS/G-32
18/SB-114
Atlanta, GA  30333
(404) 639-3590 
jeanine.bartl...@cdc.hhs.gov


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[Histonet] RE: paraffin block mailers

2010-10-25 Thread Shirley A. Powell
Hi Jeanine, 

At the NSH vendors I got a sample of a neat clear plastic holder from Source 
Medical Products, www.sourcemp.com, 1866-735-9965, holds 4 maybe 8 blocks for 
mailing, depending upon the thickness.  

Shirley


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Bartlett, 
Jeanine (CDC/OID/NCZVED)
Sent: Monday, October 25, 2010 9:50 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] paraffin block mailers

Hi everyone,

Does anyone know of a source for packaging exclusive to mailing paraffin
blocks?  Vendors please feel free to reply as well.

Thanks!

Jeanine Bartlett, BS, HT(ASCP)QIHC
Centers for Disease Control and Prevention
Infectious Diseases Pathology Branch
1600 Clifton Road, MS/G-32
18/SB-114
Atlanta, GA  30333
(404) 639-3590 
jeanine.bartl...@cdc.hhs.gov


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[Histonet] Microwave protocols

2010-10-25 Thread histotech
Hi Histonetters!

I am back with some questions on protocols for microwave processing.  We
have the Milestone processor.  For any of  you out there who use the
Milestone, do you find the pre-programmed processing runs reasonable for
your use or have you modified them?  If modified, would you be willing to
share your modifications?

Next thought, do you process your breast needle core
biopsies/lumpectomies/mastectomies etc in the microwave?  I understand that
they would have to properly fix in formalin for the minimum of 6 hours, but
do you then process conventionally or with the MW?  Does anyone have any
thoughts as to whether or not the microwave would compromise the Her2/ER/PR
results?

Does anyone have any other pitfalls/thoughts/concerns that I need to keep in
mind when using the microwave processors?

THANKS for your help!

Michelle


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[Histonet] Temporary Scientific Associate, Histology, spring 2011

2010-10-25 Thread James Watson


GNF is currently seeking a temporary Scientific Associate to join the Histology 
group, for the beginning of March 2011 through the end of July 2011. Perform 
necropsies, tissue processing, slide sectioning, routine staining, special 
staining, immunohistochemical staining and complex procedures necessary in 
preparing specimens of animal tissue in a research environment.
Qualifications:
Associate's or B.S. degree in a biological science or completion of a NAACLS 
accredited School of Histotechnology is required.  American Society of Clinical 
Pathologist (ASCP) certification as a HT or HTL is required. Applicants must 
demonstrate the potential ability to perform the essential functions of the job 
as outlined in the position description. The employee must have 2-5 years of 
experience in the Histology lab performing animal techniques, a wide variety of 
manual histochemical and enzymatic staining, automated and manual 
immunohistochemistry, and automated and manual in-situ hybridization.
Essential Functions:
1. Identifies significant tissue elements microscopically to determine quality 
of staining.
2. Necropsy, fix, trim, process, and embed animal tissue for paraffin and 
frozen sections.
3. Performs Microtomy on rotary microtome, cryostat, and be able to use a 
sliding microtome.
4. Prepares dyes and solutions in order to perform routine, special, and 
complex procedures.
5. Have experience in histochemical stains and enzymatic histochemical stains. 
Be able to trouble shoot and correct problems with histochemical stains.  Have 
experience in Immunohistochemical staining and other advanced histological 
procedures.
6. Maintains lab work area by performing preventative maintenance on 
instruments and equipment and keeping the work area clean and orderly.
7. Operate Slide scanning Instrumentation.
Interested candidates please send a copy of your CV with a summary of research 
experience, and three references.

Job Code: JW10-013

Contact:E-mail: j...@gnf.orgmailto:j...@gnf.org



James Watson HT  ASCP
Facilities Manager of Histology
GNF  Genomics Institute of the Novartis Research Foundation
Tel858-332-4647
Fax   858-812-1915mailto:858-812-1915jwat...@gnf.org
jwat...@gnf.org

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[Histonet] FW: Saponin Technique

2010-10-25 Thread Hannen, Valerie
 



From: Hannen, Valerie 
Sent: Monday, October 25, 2010 11:39 AM
To: 'histo...@list.utsouthwestern.edu'
Subject: Saponin Technique


Hi folks..
I am hoping someone out there in Histo-land can help. One of our
Pathologists is asking us to check into doing the Saponin Technique to
lyse the red cells in some of our cytology specimens. She gave a copy of
one of the pages from one of her manuals, and it shows that in order for
us to do this we would need to buy alot of reagents that we currently do
not have. Being that we would probably not be doing this technique very
often, and not sure how cost effective it will be for us to buy the
reagents, we are wondering if  anyone knows of a commercial product that
we can buy that would be a cheaper way out.
 
Thanks in advance!!
Valerie Hannen, Histotechnologist
Parrish Medical Center
Titusville,Florida


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[Histonet] RE: Saponin Technique

2010-10-25 Thread McMahon, Loralee A
It's been a while but I think that we used to add a little diluted glacial 
acetic acid to our cytology specimens to lyse the red cells. 
Not sure on the dilution, but maybe someone else knows. 



Loralee McMahon, HTL (ASCP)
Immunohistochemistry Supervisor
Strong Memorial Hospital
Department of Surgical Pathology
(585) 275-7210

From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Hannen, Valerie 
[valerie.han...@parrishmed.com]
Sent: Monday, October 25, 2010 11:39 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] FW: Saponin Technique



From: Hannen, Valerie
Sent: Monday, October 25, 2010 11:39 AM
To: 'histo...@list.utsouthwestern.edu'
Subject: Saponin Technique


Hi folks..
I am hoping someone out there in Histo-land can help. One of our
Pathologists is asking us to check into doing the Saponin Technique to
lyse the red cells in some of our cytology specimens. She gave a copy of
one of the pages from one of her manuals, and it shows that in order for
us to do this we would need to buy alot of reagents that we currently do
not have. Being that we would probably not be doing this technique very
often, and not sure how cost effective it will be for us to buy the
reagents, we are wondering if  anyone knows of a commercial product that
we can buy that would be a cheaper way out.

Thanks in advance!!
Valerie Hannen, Histotechnologist
Parrish Medical Center
Titusville,Florida


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delivering the message to the intended recipient, you are
hereby notified that any dissemination, distribution, or
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[Histonet] RE: Saponin Technique

2010-10-25 Thread Tom McNemar
I don't know about the procedure you have but ours only uses a 1% solution of 
saponin, a 3% solution of calcium gluconate, and a balanced salt solution.   We 
get the balanced salt solution from our pharmacy.


Tom McNemar, HT(ASCP)
Histology Co-ordinator
Licking Memorial Health Systems
(740) 348-4163
(740) 348-4166
tmcne...@lmhealth.org
www.LMHealth.org


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Hannen, Valerie
Sent: Monday, October 25, 2010 11:40 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] FW: Saponin Technique





From: Hannen, Valerie
Sent: Monday, October 25, 2010 11:39 AM
To: 'histo...@list.utsouthwestern.edu'
Subject: Saponin Technique


Hi folks..
I am hoping someone out there in Histo-land can help. One of our
Pathologists is asking us to check into doing the Saponin Technique to
lyse the red cells in some of our cytology specimens. She gave a copy of
one of the pages from one of her manuals, and it shows that in order for
us to do this we would need to buy alot of reagents that we currently do
not have. Being that we would probably not be doing this technique very
often, and not sure how cost effective it will be for us to buy the
reagents, we are wondering if  anyone knows of a commercial product that
we can buy that would be a cheaper way out.

Thanks in advance!!
Valerie Hannen, Histotechnologist
Parrish Medical Center
Titusville,Florida


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[Histonet] Saponin

2010-10-25 Thread Tench, Bill
Lots of blood can be a problem in cyto specimens, especially smears.  If
you are making smears from fresh specimens in particular you may elute
the obscuring hemoglobin by dipping the smear directly in acid alcohol
(i think 5% hcl-95% etoh).  We do this frequently for CT guided FNA's
(particularly of the liver and thyroid, which tend to be bloody).  We
also do this post facto on those smears even when they have already
been stained with H and E.  The red cell stroma disappears into the
background).  Just lift the coverslip and back up to 95%, use acid
alcohol ( i think it is sold on the commercial market as
differentiating agent), and then start staining process all over.
With fresh specimens you can see the hemoglobin elute from the surface
while you dip the slide.  We typically go back into regular 95% Etoh
just to get rid of the acid background (effects the blueing down the
line).
 
Bill Tench
Associate Dir. Laboratory Services
Chief, Cytology Services
Palomar Medical Center
555 E. Valley Parkway
Escondido, California  92025
bill.te...@pph.org
Voice: 760- 739-3037
Fax: 760-739-2604
 

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[Histonet] A Good Human Brain Control

2010-10-25 Thread Candice Smoots
Hi Histonetters,


I was wondering if any one could tell me where can I find a human brain amyloid 
control. I just need some suggestions  on where to order them ( control slides) 
from. Please feel free to list  any suggestions.
 

Thanks



  
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Fwd: [Histonet] FW: Saponin Technique

2010-10-25 Thread Brandi Higgins
-- Forwarded message --
From: Brandi Higgins brandihigg...@gmail.com
Date: Mon, Oct 25, 2010 at 12:08 PM
Subject: Re: [Histonet] FW: Saponin Technique
To: Hannen, Valerie valerie.han...@parrishmed.com


We use Carnoy's to lyse the red blood cells.  We get thyroid and lymph node
FNA's regularly and we always process the slides through the Carnoy's.  The
solution we use is 120 ml 95% alcohol, 60 ml chloroform, and 20 ml glacial
acetic acid.  This 200 ml solution is good for the regular sized container
for a full rack of slides, but if you only have a few slides and not a whole
rack you can use 12 ml, 6 ml, 2ml (or any ratio you want obviously) so as
not to waste solution.  We place slides in Carnoy's for 5 minutes.  The
literature says 3-5 minutes, and not to exceed 15 minutes and you may
require more time in the hematoxlin following this procedure, although we
have not found that to be necessary.  Also please note that the solution
must be prepared fresh before use.  We already had glacal acetic acid on
hand when we started using Carnoy's so we just had to order chloroform.

Brandi Higgins, BS, H(ASCP)



On Mon, Oct 25, 2010 at 11:39 AM, Hannen, Valerie 
valerie.han...@parrishmed.com wrote:



 

 From: Hannen, Valerie
 Sent: Monday, October 25, 2010 11:39 AM
 To: 'histo...@list.utsouthwestern.edu'
 Subject: Saponin Technique


 Hi folks..
 I am hoping someone out there in Histo-land can help. One of our
 Pathologists is asking us to check into doing the Saponin Technique to
 lyse the red cells in some of our cytology specimens. She gave a copy of
 one of the pages from one of her manuals, and it shows that in order for
 us to do this we would need to buy alot of reagents that we currently do
 not have. Being that we would probably not be doing this technique very
 often, and not sure how cost effective it will be for us to buy the
 reagents, we are wondering if  anyone knows of a commercial product that
 we can buy that would be a cheaper way out.

 Thanks in advance!!
 Valerie Hannen, Histotechnologist
 Parrish Medical Center
 Titusville,Florida


 **
 This email is intended solely for the use of the individual to
 whom it is addressed and may contain information that is
 privileged, confidential or otherwise exempt from disclosure
 under applicable law. If the reader of this email is not the
 intended recipient or the employee or agent responsible for
 delivering the message to the intended recipient, you are
 hereby notified that any dissemination, distribution, or
 copying of this communication is strictly prohibited. If you
 have received this communication in error, please immediately
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[Histonet] RE: Saponin

2010-10-25 Thread Sharon . Davis-Devine
Why use Saponin when you can get a commercially prepared solution such as 
Lysing 1000, which was specifically designed to remove rbc's from Cytology 
specimens.  Lysing 1000 not only lyses the rbc's but gives you exceptionally 
preserved cellular material which is amiable with IHC staining. Lysing 1000 is 
available from Obiter Research, LLC (www.obires.com) and only costs $25 per 
gallon. We have used it on all of our non-Gyn and FNA specimens for over 12 
years now. We use it instead of 95% alcohol for our FNA smears. We prepare a 
smear, air dry one for a diff quik stain and immediately immerse the other on 
in a Coplin jar of Lysing 1000.  It removes the rbc's while immediately fixing 
the cells present on the slide. I recommend using plus slides so the cells 
don't fall off.  We then rinse the needle in a container of Lysing 1000 which 
lyses the rbc's and leaves you with a very cellular specimen for a cell block.  
We have valildated it's use with IHC staining using our Ventana Benchmarks and 
seem to get consistently excellent staining results on our cell blocks. I 
highly recommend it over Carnoys and Saponin.  Let me know if you have any 
questions.

Sharon Davis-Devine, CT (ASCP)
Cytology-Histology  Supervisor
Carle Foundation Hospital
Laboratory and Pathology Services
611 West Park Street
Urbana, Illinois 61801
217-383-3572
sharon.davis-dev...@carle.com
 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tench, Bill
Sent: Monday, October 25, 2010 10:56 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Saponin

Lots of blood can be a problem in cyto specimens, especially smears.  If
you are making smears from fresh specimens in particular you may elute
the obscuring hemoglobin by dipping the smear directly in acid alcohol
(i think 5% hcl-95% etoh).  We do this frequently for CT guided FNA's
(particularly of the liver and thyroid, which tend to be bloody).  We
also do this post facto on those smears even when they have already
been stained with H and E.  The red cell stroma disappears into the
background).  Just lift the coverslip and back up to 95%, use acid
alcohol ( i think it is sold on the commercial market as
differentiating agent), and then start staining process all over.
With fresh specimens you can see the hemoglobin elute from the surface
while you dip the slide.  We typically go back into regular 95% Etoh
just to get rid of the acid background (effects the blueing down the
line).
 
Bill Tench
Associate Dir. Laboratory Services
Chief, Cytology Services
Palomar Medical Center
555 E. Valley Parkway
Escondido, California  92025
bill.te...@pph.org
Voice: 760- 739-3037
Fax: 760-739-2604
 

[None] made the following annotations
-
Confidential E-Mail: 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 otherwise protected from disclosure. Dissemination, 
distribution, or copying of this e-mail or the information herein by anyone 
other than the intended recipient is prohibited. If you have received this 
e-mail in error, please notify the sender by reply e-mail, and destroy the 
original message and all copies. 
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RE: [Histonet] A Good Human Brain Control

2010-10-25 Thread sgoebel
American Matertech


Sarah Goebel, B.A., HT (ASCP)

Histotechnician


XBiotech USA Inc.

8201 East Riverside Dr. Bldg 4 Suite 100

Austin, Texas  78744

(512)386-2907




 Original Message 
Subject: [Histonet] A Good Human Brain Control
From: Candice Smoots candice_cami...@yahoo.com
Date: Mon, October 25, 2010 9:08 am
To: histonet@lists.utsouthwestern.edu

Hi Histonetters,


I was wondering if any one could tell me where can I find a human brain
amyloid 
control. I just need some suggestions on where to order them ( control
slides) 
from. Please feel free to list any suggestions.
 

Thanks



 
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[Histonet] Thanks everyone!

2010-10-25 Thread Kendall Neely
Thank you to everyone who provided input on preferences for HE stainers last 
week. You were all very helpful!

Kendall A. Neely
Histology Technical Specialist
Shands Rocky Point Laboratories
(352) 265-0111, x72113


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[Histonet] Director of Clinical Lab needed can you help?

2010-10-25 Thread Pam Barker
Hi Histonetters!
I hope everyone is having a great day.   I just got a new position that
I want to tell you about .  The position is Clinical Lab Director.  The
position is with a hospital system and you would have the lab managers
from the 5 affiliated labs reporting to you.  The position is in AR.
Please let me know if you would be interested or know of someone who
might be interested.  Thanks-Pam


Thank You!
 
 
Pam Barker
President
RELIA 
Specialists in Allied Healthcare Recruiting
5703 Red Bug Lake Road #330
Winter Springs, FL 32708-4969
Phone: (407)657-2027
Cell: (407)353-5070
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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[Histonet] Pouring Chemicals in Stainer

2010-10-25 Thread Vanessa Avalos
I was  curious about any tricks out there for avoiding spills when setting
up the stainer. We will be receiving a new stainer soon which will be taller
and larger than our current one.  I'm just worried I will spill chemical
into the surrounding dishes. Would using wash bottles work or are there any
other ideas out there?

 

V.Avalos

ADS, INC

Fax:602-277-2134

 

 

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[Histonet] Xylene Substitute

2010-10-25 Thread Sheila Haas
Hi all!
I'm looking for recommendations for a xylene substitute for our processing and 
staining. We have two VIP's and a Leica stainer. We use Permount for 
coverslipping (manually with glass). Does anyone use a xylene substitute 
that you would recommend for this combination?
Thank you!

 
Sheila Haas
Laboratory Supervisor
MicroPath Laboratories, Inc.



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RE: [Histonet] Xylene Substitute

2010-10-25 Thread histotech
Sheila,

You might want to talk to the Leica rep.  My guy was here a couple of weeks
ago and they have a xylene sub and a mouting media that plays nicely with
it.  I don't recall the name of the product, but it might be worth talking
to him about it.

Good Luck!

Michelle

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sheila Haas
Sent: Monday, October 25, 2010 3:07 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Xylene Substitute


Hi all!
I'm looking for recommendations for a xylene substitute for our processing
and 
staining. We have two VIP's and a Leica stainer. We use Permount for 
coverslipping (manually with glass). Does anyone use a xylene substitute 
that you would recommend for this combination?
Thank you!

 
Sheila Haas
Laboratory Supervisor
MicroPath Laboratories, Inc.


  
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[Histonet] Rubber cutting mats with adhesive backs

2010-10-25 Thread Bruce W Brodersen

Why did they quit making them and what are others using as a replacement?

Bruce W. Brodersen, DVM, PhD
University of Nebraska Veterinary Diagnostic Center
1900 N. 42nd Street
Lincoln, NE  68583-0907

voice (402) 472-1434
FAX (402 472-3094
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RE: [Histonet] Xylene Substitute

2010-10-25 Thread Goins, Tresa
We use Clear-Rite 3 (Richard Allan Scientific 6901) from Fisher Scientific in 
our VIP processor and for staining.  I am not familiar with Permount, but we 
use Richard-Allan Mounting Medium (4111; also available from Fisher Scientific) 
that is toluene based - works great in combination with Clear-Rite 3.


Tresa Goins
Veterinary Diagnostic Lab
Department of Livestock
Bozeman, Montana

  

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sheila Haas
Sent: Monday, October 25, 2010 1:07 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Xylene Substitute

Hi all!
I'm looking for recommendations for a xylene substitute for our processing and 
staining. We have two VIP's and a Leica stainer. We use Permount for 
coverslipping (manually with glass). Does anyone use a xylene substitute 
that you would recommend for this combination?
Thank you!

 
Sheila Haas
Laboratory Supervisor
MicroPath Laboratories, Inc.


  
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RE: [Histonet] RE: Saponin Technique

2010-10-25 Thread Tony Henwood
The following has been found useful in my hands:

Removal of Excess Blood 
Haemolysing haemorrhagic specimens cause fewer problems in identifying
individual cells. The removal of red blood cells can be achieved using
Ficoll-Hypaque gradient separation or using a lysis solution such as
isotonic ammonium chloride (Kuenen-Boumiester etal (1996) Acta Cytolog
40:475-479.):

SOLUTIONS:
1.  Lysis solution
Ammonium Chloride4.5g
Potassium carbonate  0.5g
EDTA 0.0186g
Distilled water  500mls
2.  Hanks medium
METHOD:
1.  Centrifuge bloody fluid.
2.  Remove supernatant and add equal volume of lysis solution.
3.  Resuspend and incubate for 5 minutes at 4oC.
4.  Centrifuge, if blood still remains, then repeat from step 2.
5.  Resuspend pellet in Hanks.

Regards

Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager  Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead 
Cnr Hawkesbury Road and Hainsworth Street, Westmead 
Locked Bag 4001, Westmead NSW 2145, AUSTRALIA 




-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of McMahon,
Loralee A
Sent: Tuesday, 26 October 2010 2:51 AM
To: Hannen, Valerie; histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: Saponin Technique


It's been a while but I think that we used to add a little diluted
glacial acetic acid to our cytology specimens to lyse the red cells. 
Not sure on the dilution, but maybe someone else knows. 



Loralee McMahon, HTL (ASCP)
Immunohistochemistry Supervisor
Strong Memorial Hospital
Department of Surgical Pathology
(585) 275-7210

From: histonet-boun...@lists.utsouthwestern.edu
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Hannen, Valerie
[valerie.han...@parrishmed.com]
Sent: Monday, October 25, 2010 11:39 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] FW: Saponin Technique



From: Hannen, Valerie
Sent: Monday, October 25, 2010 11:39 AM
To: 'histo...@list.utsouthwestern.edu'
Subject: Saponin Technique


Hi folks..
I am hoping someone out there in Histo-land can help. One of our
Pathologists is asking us to check into doing the Saponin Technique to
lyse the red cells in some of our cytology specimens. She gave a copy of
one of the pages from one of her manuals, and it shows that in order for
us to do this we would need to buy alot of reagents that we currently do
not have. Being that we would probably not be doing this technique very
often, and not sure how cost effective it will be for us to buy the
reagents, we are wondering if  anyone knows of a commercial product that
we can buy that would be a cheaper way out.

Thanks in advance!!
Valerie Hannen, Histotechnologist
Parrish Medical Center
Titusville,Florida


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