RE: [Histonet] Microtome draft shield

2011-07-25 Thread Gomez, Milton
negative pressure will make the ribbons have a flying party.  is it feassible 
to built a room within the lab with no pressure for sectioning?

mg


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rathborne, Toni 
[trathbo...@somerset-healthcare.com]
Sent: Tuesday, July 19, 2011 9:11 AM
To: 'Keri Colwell'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Microtome draft shield

Haven't seen anything that specific, but you might want to look at the various 
biohazard splash guards. They are a clear Plexiglas, and they have a base to 
support them. You would be able to move them around (or have them mounted to 
the counter if desired), and they come in an assortment of angles and sizes.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Keri Colwell
Sent: Monday, July 18, 2011 5:21 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Microtome draft shield

Hi Everyone,

I work in a lab which is under negative pressure (air is continuously flowing 
in), and due to the layout of the rooms are microtomes are located next to two 
different doorways.  We are looking for some sort of draft shield to place 
around each microtome and water bath that will reduce the effects of the 
airflow and personnel movements on our ribbons.

Anyone have any suggestions as to who might sell such a thing?

Thanks in advance!




Keri Colwell
Laboratory Technologist | Technologiste de laboratoire TSE and Pathology 
Lethbridge Laboratory | Laboratoire de Lethbridge Canadian Food Inspection 
Agency | Agence candienne d'inspection des aliments Township Road 9-1 | Ch de 
Canton 9-1 Box 640  | CP 640 Lethbridge, AB T1J 3Z4 E-mail | Courriel: 
keri.colw...@inspection.gc.ca Telephone | Téléphone:  403-382-5500 Facsimile | 
Télécopieur: 403-382-5583 Government of Canada | Gouvernement du Canada

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[Histonet] HE protocol question

2011-07-25 Thread histot...@imagesbyhopper.com
Hi Histonetters!

I'm looking for thoughts on preferences/pros/cons between using a progressive 
and a regressive HE on routine daily work.

Which hematoxylins do you prefer (commercially prepared), which eosin?

Anyone have a tried and true protocol for each method?

Thanks!

Michelle

Sent from my iPhone
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[Histonet] Invitation to connect on LinkedIn

2011-07-25 Thread Thomas Huynh via LinkedIn
LinkedIn





Thomas Huynh requested to add you as a connection on LinkedIn:
  
--

David,

I'd like to add you to my professional network on LinkedIn.

- Thomas

Accept invitation from Thomas Huynh
http://www.linkedin.com/e/yvpgd1-gqjdaufb-1q/qXtGZ0-QiF70UPNqEunZRx9zbUTaXy-_ifnGa0-b4uheRh4MMF/blk/I136816395_13/1BpC5vrmRLoRZcjkkZt5YCpnlOt3RApnhMpmdzgmhxrSNBszYPclYRejcScjwScP59bQRLsDpOqkRVbP8QcjcOe3oRcPcLrCBxbOYWrSlI/EML_comm_afe/

View invitation from Thomas Huynh
http://www.linkedin.com/e/yvpgd1-gqjdaufb-1q/qXtGZ0-QiF70UPNqEunZRx9zbUTaXy-_ifnGa0-b4uheRh4MMF/blk/I136816395_13/3cNnPkVcPoNe3oPckALqnpPbOYWrSlI/svi/
 
--

DID YOU KNOW LinkedIn can help you find the right service providers using 
recommendations from your trusted network? Using LinkedIn Services, you can 
take the risky guesswork out of selecting service providers by reading the 
recommendations of credible, trustworthy members of your network. 
http://www.linkedin.com/e/yvpgd1-gqjdaufb-1q/svp/inv-25/
 
-- 
(c) 2011, LinkedIn Corporation
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[Histonet] Wax disposal

2011-07-25 Thread Denise Mattingly
Are the disposal issues over the
Used paraffin because of chemicals like xylene in the wax
Or is it the human tissue in the
Wax
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[Histonet] Tissue Processing: Blue Dye used to see small tissue

2011-07-25 Thread White, Lisa M.
We use Mucicarmine placed in a small dropper bottle, it does not wash
out in the processor and makes the tissues easy to see once embedded.

 

 

Lisa White, HT(ASCP)

Supervisory HT

James H. Quillen VAMC

PO Box 4000

Corner of Veterans Way and Lamont

PLMS 113

Mountain Home, TN 37684

423-979-3567

423-979-3401 fax

 

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[Histonet] Recycled alcohol

2011-07-25 Thread Webb, Dorothy L
You do not get 100% alcohol back from recycling, so it cannot be used as such 
in either the processor or stainer.  Basically, you have to use it as 95%.  
That may be your problem!!



  
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[Histonet] NBF Recycled Alc

2011-07-25 Thread Senn, Amy R
Hi all,

We dump everything (and I mean EVERYTHING) down the drain.  Formalin,
waste from Benchmark, etc.



We use 95% recycled alcohol for everything as well (stainer, making up
reagents, etc), but that's the only reagent (other than clear-rite) that
we use recycled. Our 100% alcohol is right from the bottle.

We check our 95 also, and if it's not a 'true' 95, it gets dumped.



Thanks



Amy R.

Holy Spirit Health System

503 N. 21st Street

Camp Hill, PA 17011

Phone: 717-763-2124

Fax: 717-763-2947

www.hsh.org









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[Histonet] PARAFFIN WASTE

2011-07-25 Thread Sara Baldwin/mhhcc.org
Our paraffin is also hauled off with hazardous waste
Thanks
Pathology Supervisor
S. Kathy Baldwin, SCT (ASCP)
Memorial Hospital and Health Care Center
sbald...@mhhcc.org
Ph 812-482-0210, 0216,  Fax 812-482-0232, 
Pager 812-481-0897, Cell 812-887-3357
Confidential information, Authorized use only.
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[Histonet] ki67/mart 1 double stain

2011-07-25 Thread Sara Baldwin/mhhcc.org
I  have  a protocol I will share from the benchmark lt  for dual stains if you 
want to e-mail me directly!
 
Thanks
Pathology Supervisor
S. Kathy Baldwin, SCT (ASCP)
Memorial Hospital and Health Care Center
sbald...@mhhcc.org
Ph 812-482-0210, 0216,  Fax 812-482-0232, 
Pager 812-481-0897, Cell 812-887-3357
Confidential information, Authorized use only.
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[Histonet] Frozen eye problems

2011-07-25 Thread Boyce, Bobbie
Hello Histoneters,

I'm having problems getting a good section on paraformaldyehyde fixed
adult mouse eyes frozen in TBS tissue freezing medium. One of the
problems was the orentation of them. They were too close to the edge. I
also, wanted to try a harder freezing medium, so I corrected oriented
and used an OCT equivalent tissue freezing medium.  They looked better,
but still not as nice as I think they should be.

My eye contact tells me that they should be cut at -20 for adult and -14
for neonatal. They have me set the knife angle at 0 to -2.5. 

I also tried cutting these as I would cut any other frozen issue, but
I'm just pulling my hair out.

Does anyone have any other suggestions that I might try? Your help would
be greatly appreciated.

Bobbie Boyce
Histology Specialist III
duPont Hospital for Children
Wilmington, DE
302-651-6771 (Lab)
302-651-5010 (Fax)





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[Histonet] RE: Frozen eye problems

2011-07-25 Thread Anatoli Gleiberman
Try Neg-50 (Fisher, cat#22-110-617) instead of OCT, we don't have any problem 
with fresh-frozen mouse eyes.

Anatoli Gleiberman, PhD
Director of Histopathology
Cleveland Biolabs, Inc
73 High Street
Buffalo, NY 14203
phone:716-849-6810 ext.354
fax:716-849-6817
e-mail: agleiber...@cbiolabs.com

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Boyce, Bobbie
Sent: Monday, July 25, 2011 10:31 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Frozen eye problems

Hello Histoneters,

I'm having problems getting a good section on paraformaldyehyde fixed
adult mouse eyes frozen in TBS tissue freezing medium. One of the
problems was the orentation of them. They were too close to the edge. I
also, wanted to try a harder freezing medium, so I corrected oriented
and used an OCT equivalent tissue freezing medium.  They looked better,
but still not as nice as I think they should be.

My eye contact tells me that they should be cut at -20 for adult and -14
for neonatal. They have me set the knife angle at 0 to -2.5. 

I also tried cutting these as I would cut any other frozen issue, but
I'm just pulling my hair out.

Does anyone have any other suggestions that I might try? Your help would
be greatly appreciated.

Bobbie Boyce
Histology Specialist III
duPont Hospital for Children
Wilmington, DE
302-651-6771 (Lab)
302-651-5010 (Fax)





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Re: [Histonet] HE protocol question

2011-07-25 Thread Rene J Buesa
Progressive hematoxylins usually take more time to stain  and for routine work 
the schedule has to be very fine tuned because otherwise obtaining the ideal 
staining is quite difficult with a frequent tendency to the under staining.
Regressive hematoxylins on the other hand, always over stain and then you can 
obtain the ideal staining by removing the hematoxylin with acid or aqueous 
solutions. They are faster and the results are more easy to control.
For many years I always prepared my hematoxylins, but now there are commercial 
solutions of great quality and consistent results so it is better (although no 
more cost effective) to buy a reputable brand, develop a good protocol and 
stick to it. At the end I relied on Richard Allen hematoxylins.
Eosin, on the other hand, are so easy to prepare that I always prepared mine.
René J.

--- On Mon, 7/25/11, histot...@imagesbyhopper.com 
histot...@imagesbyhopper.com wrote:


From: histot...@imagesbyhopper.com histot...@imagesbyhopper.com
Subject: [Histonet] HE protocol question
To: Histonet@Lists. Utsouthwestern. Edu histonet@lists.utsouthwestern.edu
Date: Monday, July 25, 2011, 7:29 AM


Hi Histonetters!

I'm looking for thoughts on preferences/pros/cons between using a progressive 
and a regressive HE on routine daily work.

Which hematoxylins do you prefer (commercially prepared), which eosin?

Anyone have a tried and true protocol for each method?

Thanks!

Michelle

Sent from my iPhone
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[Histonet] DS MART 1/ KI 67

2011-07-25 Thread Sara Baldwin/mhhcc.org
  
FOR
BENNCHMARK LT
Procedure  XT IHC DS UDAB-URED
Depar
Cell condition short 8 min
37 degrees/default
Mart 1 32 min
Amplify
ultrawash
aby denaturation
90 deg C  4 min
37 degrees/default 
Ki67  4min
DS ultra wash 
counterstain Heme (we do 20 min on this our Path likes it dark)
usually Heme is 4  min



Thanks
Pathology Supervisor
S. Kathy Baldwin, SCT (ASCP)
Memorial Hospital and Health Care Center
sbald...@mhhcc.org
Ph 812-482-0210, 0216,  Fax 812-482-0232, 
Pager 812-481-0897, Cell 812-887-3357
Confidential information, Authorized use only.
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[Histonet] Working Ventana Probe Protocols (EBER)

2011-07-25 Thread Sebree Linda A
Hi Marc and Histonetters (especially those using XTs),
 
 
I've been trying to work up VMS's new EBER probe with less than stellar
results.
 
I have some questions about the protocols you sent via Histonet back in
early June.  My questions/protocols are in red.
 
You state the following:
 
Depar 16 min  We can only select depar without an incubation
timedoes your instrument allow you to select a time?  We are doing
this on an XT, is this an instrument difference?  What instrument are
you running your ISH onUltra by chance?
 
Enzyme Protease 2 for 4 min. We are using ISH Protease 2 / 12 mins. as
that was our protocol with the old stuff.
 
ISH (EBER) probe 4 min. Same
 
Denature @ 85 degrees for 12 min. Same
 
Hybe 1 hour What temperature are you hybridizing at? 
 
3 stringency washes for 8 minutes each At what temperature?
 
Blue detection for 20 minutes Same
 
Counterstain for 4 min We use Nuclear Fast Red for 8 mins.
 
Marc, are you using HybReady?
 
Anyone else having had some success with the new EBER probe, reagents
and software, feel free to comment.  Of the 3 specimens I've run, known
positive soft tissue, bm bx and cell block, the soft tissue and bm bx
had some positivity with the EBER DNP and U6 DNP but the cell block was
negative with both.  There was also lots of blue smearing and haze over
the slides.  I'm afraid this optimization/validation could end up being
very expensive even with our 3 control tissues picked up together on
single slides.
 
Thanks for everyone's help,
 
Linda
 

Linda A. Sebree 
University of Wisconsin Hospital  Clinics 
IHC/ISH Laboratory 
DB1-223 VAH 
600 Highland Ave. 
Madison, WI 53792 
(608)265-6596 

 
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Re: [Histonet] Working Ventana Probe Protocols (EBER)

2011-07-25 Thread Mark Tarango
Hi Linda,

I had simliar trouble before I bought and added the extra HybReady to the
protocol (there is one that comes with the detection kit, but you need two
for good staining).  It will clean up your stain and A LOT and remove those
blue splotches that show up when you don't use it.

Mark

On Mon, Jul 25, 2011 at 9:39 AM, Sebree Linda A lseb...@uwhealth.orgwrote:

 Hi Marc and Histonetters (especially those using XTs),


 I've been trying to work up VMS's new EBER probe with less than stellar
 results.

 I have some questions about the protocols you sent via Histonet back in
 early June.  My questions/protocols are in red.

 You state the following:

 Depar 16 min  We can only select depar without an incubation
 timedoes your instrument allow you to select a time?  We are doing
 this on an XT, is this an instrument difference?  What instrument are
 you running your ISH onUltra by chance?

 Enzyme Protease 2 for 4 min. We are using ISH Protease 2 / 12 mins. as
 that was our protocol with the old stuff.

 ISH (EBER) probe 4 min. Same

 Denature @ 85 degrees for 12 min. Same

 Hybe 1 hour What temperature are you hybridizing at?

 3 stringency washes for 8 minutes each At what temperature?

 Blue detection for 20 minutes Same

 Counterstain for 4 min We use Nuclear Fast Red for 8 mins.

 Marc, are you using HybReady?

 Anyone else having had some success with the new EBER probe, reagents
 and software, feel free to comment.  Of the 3 specimens I've run, known
 positive soft tissue, bm bx and cell block, the soft tissue and bm bx
 had some positivity with the EBER DNP and U6 DNP but the cell block was
 negative with both.  There was also lots of blue smearing and haze over
 the slides.  I'm afraid this optimization/validation could end up being
 very expensive even with our 3 control tissues picked up together on
 single slides.

 Thanks for everyone's help,

 Linda


 Linda A. Sebree
 University of Wisconsin Hospital  Clinics
 IHC/ISH Laboratory
 DB1-223 VAH
 600 Highland Ave.
 Madison, WI 53792
 (608)265-6596


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[Histonet] Job opening Prescott Arizona

2011-07-25 Thread Howery, Jeffrey
Just wanted to add a few details.
We are currently searching for a Cana date for our opening. We are
located in Northern Arizona in the pines. We have two Campuses with the
main campus in Prescott with the second campus located in Prescott
Valley. We are a total of Approx. 187 beds combined. Please Check out
our web site at YRMC.org to see our job opening and information about
our Hospital. Prescott Az on the web to check out the area Arizona is
full of history. We are located 1 1/2 hours north of Phoenix and the
same to Flagstaff. Sedona is about 45 mins away and the Grand Canyon 3
hours. Contact me here  for any questions and if interested fill out an
application on the YRMC web site.  Thanks for your time. Jeff

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[Histonet] Cutting frozen decalcified mouse bones

2011-07-25 Thread Adam .
Hi all,

I had a very difficult time cutting my very precious triple transgenic
frozen decalcified mouse bones this morning. As I cut into them, the
sections scrunched up into a mess of OCT pretty much as soon as the blades
hit the block. These were 4% PFA perfused and post-fixed for 24 hours,
decalcified with 14% EDTA using weight loss/weight gain as an endpoint,
cryoprotected overnight in 30% sucrose, embedded in OCT using liquid
nitrogen cooled isopentane vertically (i.e. I was cutting from one growth
plate to the other), and cut at 7 uM. Changing to a new blade didn't help.
Changing the cutting temperature from -10C to -15C didn't help. Changing the
cutting speed didn't help. I can't change the cutting angle without a
special tool, and this isn't my device so I don't want to mess with it.

The only way I could get reasonable sections was to use a tape transfer
system, which seemed like overkill to me, but I need these sections ASAP.
Ideas? I have a whole bunch more bones I need to cut over the next few
weeks...

Thanks,
Adam
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[Histonet] blurry tissue

2011-07-25 Thread Carol Bryant
I would like some thoughts on how to resolve some blurry looking tissue.  We 
have had occasional tissue that looks blurry and not crisp for several weeks 
now.  It is not all the cases only random tissues.  The tissue is not on the 
same tissue processor either. We have 2 processors.  The latest cases were a 
breast, some skins, and a prostate.  I am not certain if this is happening on 
the tissue processor or in the stainer.  It has been very humid in our lab so I 
have started running a dehumidifier in case there is water in the xylene.  It 
is so hit and miss that I am puzzled.   Any suggestions would be greatly 
appreciated.
Thank you in advance for your thoughts.

Carol Bryant, CT (ASCP)
Cytology/Histology Manager
Pathology Services
Lexington Clinic
Phone (859) 258-4082
Fax (859) 258-4081
cb...@lexclin.com



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[Histonet] Biogenex Xmatrx Infinity Stainer

2011-07-25 Thread Hughes, Anna
Hi Everyone!

I was wondering if anyone out there had and was using the Biogenex Xmatrx 
Infinity Stainer from Biogenex.  We are considering buying one to do ISH and 
FISH on, but was wondering what other people had to say about it.   Any 
feedback would be greatly appreciated!

Thanks!
Anna Hughes

Merck  Co., Inc.
West Point, PA
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[Histonet] Formalin down the drain??

2011-07-25 Thread mtitford


I was a little distressed to read the message from Amy in Camp Hill, 
Pennsylvania declaring she dumps everything (and I mean everything) from her 
histology lab down the drain. There are a bunch of Federal Laws governing 
handling and disposal of chemicals used in the histology laboratory and she 
appears to be breaking several. The wastewater law limits how much formalin you 
can discard down the sink (and you cannot dilute as you go). The same law 
forbids disposal of organic solvents like xylene, or solutions containing 
organic solvents. Local laws in Pennsylvania may be more strict.

I recommend to Amy that she purchases a book like, Hazardous materials in the 
histopathology laboratory by Janet  Richard Dapson and read the whole thing 
cover to cover!

Michael Titford
Pathology USA
Mobile AL USA

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[Histonet] Antibody suggestions for dog and cat

2011-07-25 Thread Mark Tarango
Could anyone suggest suituble antibodies for the following markers in dog
and cat tissue:

Vimentin, Pankeratin, CD3 and CD20, CD18, MelanA, Factor VIII

Also could use a suggestion for C-kit in Dog tissue only.

thanks

Mark
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[Histonet] Cerner CoPath Plus

2011-07-25 Thread Weems, Joyce
Anyone using this system, would you please contact me off line? I have 
questions regarding the PicsPlus component as well as I'm curious to see how 
everyone likes it.

Thanks! j


Joyce Weems
Pathology Manager
Saint Joseph's Hospital
5665 Peachtree Dunwoody Rd NE
Atlanta, GA 30342
678-843-7376 - Phone
678-843-7831 - Fax


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Re: [Histonet] Antibody suggestions for dog and cat

2011-07-25 Thread Jan Shivers

Hi Mark,

Vimentin - Dako; M0725, clone V9
Pankeratin - Dako; M0821; clone MNF116
CD3 - LabVision; RB-9039; rabbit polyclonal
CD20 - LabVision; RB-9013; rabbit polyclonal
CD18 (canine) - Leukocyte Antigen Biology Lab (UC-Davis; Dr. Peter Moore); 
clone CA16.3C10
CD18 (feline) - Leukocyte Antigen Biology Lab (UC-Davis; Dr. Peter Moore); 
clone FE3.9F2

Melan A - Dako; M7195; clone A103
Factor VIII - Dako; A0082; rabbit polyclonal

CD117 - Dako; A4502; rabbit polyclonal (not specific for dogs; tested 
successfully on cow and horse, also)


Let me know if you need information on any other antibodies in question.  I 
species-validate all of my  IHC tests (100+).


Jan Shivers
Senior Scientist
Histology/IHC/EM Section Head
Pathology Teaching Program
University of Minnesota
Veterinary Diagnostic Laboratory
1333 Gortner Ave.
St. Paul, MN  55108
612-624-7297
shive...@umn.edu

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- Original Message - 
From: Mark Tarango marktara...@gmail.com

To: histonet@lists.utsouthwestern.edu Histonet@lists.utsouthwestern.edu
Sent: Monday, July 25, 2011 1:33 PM
Subject: [Histonet] Antibody suggestions for dog and cat



Could anyone suggest suituble antibodies for the following markers in dog
and cat tissue:

Vimentin, Pankeratin, CD3 and CD20, CD18, MelanA, Factor VIII

Also could use a suggestion for C-kit in Dog tissue only.

thanks

Mark
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RE: [Histonet] blurry tissue

2011-07-25 Thread Johnson, Nacaela
What is the staining intensity like? 


Thanks,
 
Nacaela Johnson, B.S. HTL (ASCP)CM
Histotechnologist
KCCC Pathology
12000 110th St., Ste. 400
Overland Park, KS 66210
Office:  913-234-0576
Fax:  913-433-7639
Email:  nacaela.john...@usoncology.com

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Carol
Bryant
Sent: Monday, July 25, 2011 12:42 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] blurry tissue 

I would like some thoughts on how to resolve some blurry looking
tissue.  We have had occasional tissue that looks blurry and not crisp
for several weeks now.  It is not all the cases only random tissues.
The tissue is not on the same tissue processor either. We have 2
processors.  The latest cases were a breast, some skins, and a prostate.
I am not certain if this is happening on the tissue processor or in the
stainer.  It has been very humid in our lab so I have started running a
dehumidifier in case there is water in the xylene.  It is so hit and
miss that I am puzzled.   Any suggestions would be greatly appreciated.
Thank you in advance for your thoughts.

Carol Bryant, CT (ASCP)
Cytology/Histology Manager
Pathology Services
Lexington Clinic
Phone (859) 258-4082
Fax (859) 258-4081
cb...@lexclin.com



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Re: [Histonet] Antibody suggestions for dog and cat

2011-07-25 Thread Kathleen Jones
Hello Mark
 
We use the Ventana Benchmark for most of our IHC. We don't use all of
the markers you listed, but and for our canine and feline tissue we do
have great results with the following:
Vimentin-Ventana
Cytokeratin-Dako
CD18-UC-Davis (Dr. Peter Moore)
C-kit-Dako
 
We worked hard to get the Melan A (Dako) working but had trouble with
using a DAB detection kit..perhaps a red kit would be better.
 
If you would like more info, feel free to contact me directly.
 
Kathy
 
Kathleen Jones
Research Technologist
Pathology/Microbiology
AVC - UPEI
(902)566-0595


 Mark Tarango marktara...@gmail.com 25/07/2011 3:33 PM 
Could anyone suggest suituble antibodies for the following markers in
dog
and cat tissue:

Vimentin, Pankeratin, CD3 and CD20, CD18, MelanA, Factor VIII

Also could use a suggestion for C-kit in Dog tissue only.

thanks

Mark
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[Histonet] Looking for assistance in Southeast part of the country-

2011-07-25 Thread Jon Arnold
Hello-
Is there anyone in the southeast part of the country with familiarity with the:

Shandon Hypercenter XP tissue processor?
Leica ST5050 IHC stainer (Jung Immunostainer)?

I was looking for someone with experience with either of these that may be 
interested and able to pass along some knowledge to 'new' users of the 
instruments.

Thank you in advance-

Regards-

Jon Arnold
T: 1-800-745-2710 | F: 763-712-8724


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RE: [Histonet] Formalin down the drain??

2011-07-25 Thread Rathborne, Toni
Michael,
Since this seems to come up somewhat regularly, if you do have a link to the 
federal laws which govern this, maybe you could share. I'm sure this would help 
labs get the support they need for proper disposal.
Toni

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of mtitf...@aol.com
Sent: Monday, July 25, 2011 1:59 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Formalin down the drain??



I was a little distressed to read the message from Amy in Camp Hill, 
Pennsylvania declaring she dumps everything (and I mean everything) from her 
histology lab down the drain. There are a bunch of Federal Laws governing 
handling and disposal of chemicals used in the histology laboratory and she 
appears to be breaking several. The wastewater law limits how much formalin you 
can discard down the sink (and you cannot dilute as you go). The same law 
forbids disposal of organic solvents like xylene, or solutions containing 
organic solvents. Local laws in Pennsylvania may be more strict.

I recommend to Amy that she purchases a book like, Hazardous materials in the 
histopathology laboratory by Janet  Richard Dapson and read the whole thing 
cover to cover!

Michael Titford
Pathology USA
Mobile AL USA

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[Histonet] Need a protocol for CD24 and CD133

2011-07-25 Thread dusko trajkovic




Hi.
Does anyone out there have a protocol for CD24 and CD133 that will work on 
mouse 
Xenograft tumors? Preferably a protocol that will work on Leica Bond, but any 
working protocol will do at this point.
Thank you and have a good day.
Dusko
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[Histonet] Biocare decloaker

2011-07-25 Thread Diana McCaig
We are trying to validate a Biocare decloaker and have found when we use
122 degrees for 30 seconds we get great signal, but distorted
morphology.

 

If we reduce to 90 degrees for  45 minutes, the signal is significantly
decreased but the morphology is good.

 

What protocols are you using?

 

Diana

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RE: [Histonet] Formalin down the drain??

2011-07-25 Thread O'Donnell, Bill
One should not automtically assume that laws are broken here. 

(Rant begins here)

First of all, it is the States that set the limits of what can and
cannot be dumped. All States must meet Federal standards,but States are
free to determine how they do that. (It's one of the benefits of the
American Revolution) Some states are more heavily regulated than others.
California and Colorado come to mind immediately.

Different organizations, locations and circumstances may allow for
disposal of products that may be diluted to such a degree as to be
negligable in the waste stream. Our institution generates 65,000 gallons
of waste water daily, which allows us to make the dilution limits of
anything that our histo lab could produce in a day. 

No laws are broken if I should pour xylene, formalin, alcohols or other
common compounds that we might generate on even our busiest days into
the waste stream. 

HOWEVER, while we may be allowed to do so by state and local
regulations, we have decided it is not prudent to do so and so we
collect, ship, neutralize or recycle most all that the histo lab
generates. We do this at the lab level, with lab funding. It is the
responsible thing to do, and we are morally and ethically bound to do
so, but we are not outside the law if we do not.

If your local municipal waste systems people give you the green light on
dumping formalin down the drain. you are not breaking the law,
federal or otherwise, in doing so. 

It is true that if you wish to affect things globally, one has to be
responsible locally.

Here is what my rant comes down to Make certain that you are meeting
local standards for your chemical disposal or you may well be breaking
the law. And a big thank you (from myself, my children, grandchildren
and great-grand children and that lady who sells me the slurpee at the
local convenience store) for anything anyone is doing above and beyond
that. 

:)Rant is over... Have a nice day :)  

You cannot Like this rant on Facebook or follow this rant on Twitter. 

Bill


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
mtitf...@aol.com
Sent: Monday, July 25, 2011 12:59 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Formalin down the drain??



I was a little distressed to read the message from Amy in Camp Hill,
Pennsylvania declaring she dumps everything (and I mean everything)
from her histology lab down the drain. There are a bunch of Federal Laws
governing handling and disposal of chemicals used in the histology
laboratory and she appears to be breaking several. The wastewater law
limits how much formalin you can discard down the sink (and you cannot
dilute as you go). The same law forbids disposal of organic solvents
like xylene, or solutions containing organic solvents. Local laws in
Pennsylvania may be more strict.

I recommend to Amy that she purchases a book like, Hazardous materials
in the histopathology laboratory by Janet  Richard Dapson and read the
whole thing cover to cover!

Michael Titford
Pathology USA
Mobile AL USA

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RE: [Histonet] Formalin down the drain??

2011-07-25 Thread Blazek, Linda
I may not be able to Like Bill's rant, but I second it.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of O'Donnell, Bill
Sent: Monday, July 25, 2011 4:20 PM
To: mtitf...@aol.com; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Formalin down the drain??

One should not automtically assume that laws are broken here. 

(Rant begins here)

First of all, it is the States that set the limits of what can and
cannot be dumped. All States must meet Federal standards,but States are
free to determine how they do that. (It's one of the benefits of the
American Revolution) Some states are more heavily regulated than others.
California and Colorado come to mind immediately.

Different organizations, locations and circumstances may allow for
disposal of products that may be diluted to such a degree as to be
negligable in the waste stream. Our institution generates 65,000 gallons
of waste water daily, which allows us to make the dilution limits of
anything that our histo lab could produce in a day. 

No laws are broken if I should pour xylene, formalin, alcohols or other
common compounds that we might generate on even our busiest days into
the waste stream. 

HOWEVER, while we may be allowed to do so by state and local
regulations, we have decided it is not prudent to do so and so we
collect, ship, neutralize or recycle most all that the histo lab
generates. We do this at the lab level, with lab funding. It is the
responsible thing to do, and we are morally and ethically bound to do
so, but we are not outside the law if we do not.

If your local municipal waste systems people give you the green light on
dumping formalin down the drain. you are not breaking the law,
federal or otherwise, in doing so. 

It is true that if you wish to affect things globally, one has to be
responsible locally.

Here is what my rant comes down to Make certain that you are meeting
local standards for your chemical disposal or you may well be breaking
the law. And a big thank you (from myself, my children, grandchildren
and great-grand children and that lady who sells me the slurpee at the
local convenience store) for anything anyone is doing above and beyond
that. 

:)Rant is over... Have a nice day :)  

You cannot Like this rant on Facebook or follow this rant on Twitter. 

Bill


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
mtitf...@aol.com
Sent: Monday, July 25, 2011 12:59 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Formalin down the drain??



I was a little distressed to read the message from Amy in Camp Hill,
Pennsylvania declaring she dumps everything (and I mean everything)
from her histology lab down the drain. There are a bunch of Federal Laws
governing handling and disposal of chemicals used in the histology
laboratory and she appears to be breaking several. The wastewater law
limits how much formalin you can discard down the sink (and you cannot
dilute as you go). The same law forbids disposal of organic solvents
like xylene, or solutions containing organic solvents. Local laws in
Pennsylvania may be more strict.

I recommend to Amy that she purchases a book like, Hazardous materials
in the histopathology laboratory by Janet  Richard Dapson and read the
whole thing cover to cover!

Michael Titford
Pathology USA
Mobile AL USA

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[Histonet] Where Can I Buy Pneumo Control Slides

2011-07-25 Thread Wanda.Smith
Good Afternoon to All,
I am getting pretty desperate to find a source for Pneumo control slides.  I 
know they are hard to come by, but my favorite source Newcomer Supply does not 
have any and I ordered some from Sigma-Aldrich and now they are discontinued.  
Please Help!
Thanks,
Wanda

WANDA G. SMITH, HTL(ASCP)HT
Pathology Supervisor
TRIDENT MEDICAL CENTER
9330 Medical Plaza Drive
Charleston, SC  29406
843-847-4586
843-847-4296 fax


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RE: [Histonet] Biocare decloaker

2011-07-25 Thread Mike Pence
There is a huge difference between 122 degrees for 30 seconds and 90
degrees for 45 minutes. I would say you need to look at something here!

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Diana
McCaig
Sent: Monday, July 25, 2011 2:45 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Biocare decloaker


We are trying to validate a Biocare decloaker and have found when we use
122 degrees for 30 seconds we get great signal, but distorted
morphology.

 

If we reduce to 90 degrees for  45 minutes, the signal is significantly
decreased but the morphology is good.

 

What protocols are you using?

 

Diana

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Re: [Histonet] Biocare decloaker

2011-07-25 Thread William
As to the efficacy of retrieval, there is actually not that big of a 
difference. Biocare publishes that 90 degrees for 60 mins is roughly equivalent 
to 125 degrees for 30 seconds. 

My guess, based on limited information in the original email is that Diana 
needs a new gasket. Those should be replaced every 6 months. 

Will Chappell

Sent from my iPhone

On Jul 25, 2011, at 1:34 PM, Mike Pence mpe...@grhs.net wrote:

 There is a huge difference between 122 degrees for 30 seconds and 90
 degrees for 45 minutes. I would say you need to look at something here!
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Diana
 McCaig
 Sent: Monday, July 25, 2011 2:45 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Biocare decloaker
 
 
 We are trying to validate a Biocare decloaker and have found when we use
 122 degrees for 30 seconds we get great signal, but distorted
 morphology.
 
 
 
 If we reduce to 90 degrees for  45 minutes, the signal is significantly
 decreased but the morphology is good.
 
 
 
 What protocols are you using?
 
 
 
 Diana
 
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 Histonet@lists.utsouthwestern.edu
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RE: [Histonet] Biocare decloaker

2011-07-25 Thread Weems, Joyce
I wonder if a new gasket would help me.. I keep blowing mine! :) 


Joyce Weems 
Pathology Manager 
Saint Joseph's Hospital 
5665 Peachtree Dunwoody Rd NE 
Atlanta, GA 30342 
678-843-7376 - Phone 
678-843-7831 - Fax 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of William
Sent: Monday, July 25, 2011 16:40
To: Mike Pence
Cc: histonet@lists.utsouthwestern.edu; Diana McCaig
Subject: Re: [Histonet] Biocare decloaker

As to the efficacy of retrieval, there is actually not that big of a 
difference. Biocare publishes that 90 degrees for 60 mins is roughly equivalent 
to 125 degrees for 30 seconds. 

My guess, based on limited information in the original email is that Diana 
needs a new gasket. Those should be replaced every 6 months. 

Will Chappell

Sent from my iPhone

On Jul 25, 2011, at 1:34 PM, Mike Pence mpe...@grhs.net wrote:

 There is a huge difference between 122 degrees for 30 seconds and 90 
 degrees for 45 minutes. I would say you need to look at something here!
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Diana 
 McCaig
 Sent: Monday, July 25, 2011 2:45 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Biocare decloaker
 
 
 We are trying to validate a Biocare decloaker and have found when we 
 use
 122 degrees for 30 seconds we get great signal, but distorted 
 morphology.
 
 
 
 If we reduce to 90 degrees for  45 minutes, the signal is 
 significantly decreased but the morphology is good.
 
 
 
 What protocols are you using?
 
 
 
 Diana
 
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 Histonet@lists.utsouthwestern.edu
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Confidentiality Notice:
This e-mail, including any attachments is the 
property of Catholic Health East and is intended 
for the sole use of the intended recipient(s).  
It may contain information that is privileged and 
confidential.  Any unauthorized review, use,
disclosure, or distribution is prohibited. If you are 
not the intended recipient, please delete this message, and 
reply to the sender regarding the error in a separate email. 
 


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Re: [Histonet] blurry tissue

2011-07-25 Thread Rene J Buesa
You just pointed out to the most likely causes: happening during staining, high 
humidity and water in the xylene. Try to take care of these issues and you will 
resolve the problem.
René J.

--- On Mon, 7/25/11, Carol Bryant cb...@lexclin.com wrote:


From: Carol Bryant cb...@lexclin.com
Subject: [Histonet] blurry tissue
To: histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
Date: Monday, July 25, 2011, 1:42 PM


I would like some thoughts on how to resolve some blurry looking tissue.  We 
have had occasional tissue that looks blurry and not crisp for several weeks 
now.  It is not all the cases only random tissues.  The tissue is not on the 
same tissue processor either. We have 2 processors.  The latest cases were a 
breast, some skins, and a prostate.  I am not certain if this is happening on 
the tissue processor or in the stainer.  It has been very humid in our lab so I 
have started running a dehumidifier in case there is water in the xylene.  It 
is so hit and miss that I am puzzled.   Any suggestions would be greatly 
appreciated.
Thank you in advance for your thoughts.

Carol Bryant, CT (ASCP)
Cytology/Histology Manager
Pathology Services
Lexington Clinic
Phone (859) 258-4082
Fax (859) 258-4081
cb...@lexclin.com



NOTICE OF CONFIDENTIALITY

This message, including any attachments, is intended only for the sole use of 
the addressee and may contain confidential or privileged information that is 
protected by the State of Kentucky and/or Federal regulations.  If you are not 
the intended recipient, do not read, copy, retain or disseminate this message 
or any attachment. If you have received this message in error, please call the 
sender immediately at (859)258-4000 and delete all copies of this message and 
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or any attachment, nor any error in transmission or misdelivery shall 
constitute waiver of any applicable legal privilege. 
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Re: [Histonet] Biocare decloaker

2011-07-25 Thread William
Ok that is a bigger problem and a very clear answer to your staining issue. 
Your decloaker should never blow a gasket. Something is wrong and you 
probably need service or a replacement. Your decloaker is probably getting too 
hot and over retrieving tissue.  I suggest immediately calling Biocare 
technical support. 

You need this fixed!

Will Chappell


Sent from my iPhone

On Jul 25, 2011, at 1:42 PM, Weems, Joyce jwe...@sjha.org wrote:

 I wonder if a new gasket would help me.. I keep blowing mine! :) 
 
 
 Joyce Weems 
 Pathology Manager 
 Saint Joseph's Hospital 
 5665 Peachtree Dunwoody Rd NE 
 Atlanta, GA 30342 
 678-843-7376 - Phone 
 678-843-7831 - Fax 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of William
 Sent: Monday, July 25, 2011 16:40
 To: Mike Pence
 Cc: histonet@lists.utsouthwestern.edu; Diana McCaig
 Subject: Re: [Histonet] Biocare decloaker
 
 As to the efficacy of retrieval, there is actually not that big of a 
 difference. Biocare publishes that 90 degrees for 60 mins is roughly 
 equivalent to 125 degrees for 30 seconds. 
 
 My guess, based on limited information in the original email is that Diana 
 needs a new gasket. Those should be replaced every 6 months. 
 
 Will Chappell
 
 Sent from my iPhone
 
 On Jul 25, 2011, at 1:34 PM, Mike Pence mpe...@grhs.net wrote:
 
 There is a huge difference between 122 degrees for 30 seconds and 90 
 degrees for 45 minutes. I would say you need to look at something here!
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Diana 
 McCaig
 Sent: Monday, July 25, 2011 2:45 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Biocare decloaker
 
 
 We are trying to validate a Biocare decloaker and have found when we 
 use
 122 degrees for 30 seconds we get great signal, but distorted 
 morphology.
 
 
 
 If we reduce to 90 degrees for  45 minutes, the signal is 
 significantly decreased but the morphology is good.
 
 
 
 What protocols are you using?
 
 
 
 Diana
 
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RE: [Histonet] Formalin down the drain??

2011-07-25 Thread Rene J Buesa
Your rant is interesting but wrong.
OSHA (which is a FEDERAL agency) prohibits dumping ANY type of hazardous 
materials down the drain. 
I was also taken aback by Amy's posting.
No, regardless of what your state law may or may not permit you to dump in the 
drain, you should not put some $avings over the well being of the environment 
and the drinking water of people.
Formaldehyde is toxic and recently officially declared carcinogen.
In the same way that frackting methods to obtain gas from shale has been 
deemed dangerous, equally dumping formaldehyde, xylene and any other chemical 
ought to be the source of concern. This in my rant!
René J.

--- On Mon, 7/25/11, O'Donnell, Bill billodonn...@catholichealth.net wrote:


From: O'Donnell, Bill billodonn...@catholichealth.net
Subject: RE: [Histonet] Formalin down the drain??
To: mtitf...@aol.com, histonet@lists.utsouthwestern.edu
Date: Monday, July 25, 2011, 4:19 PM


One should not automtically assume that laws are broken here. 

(Rant begins here)

First of all, it is the States that set the limits of what can and
cannot be dumped. All States must meet Federal standards,but States are
free to determine how they do that. (It's one of the benefits of the
American Revolution) Some states are more heavily regulated than others.
California and Colorado come to mind immediately.

Different organizations, locations and circumstances may allow for
disposal of products that may be diluted to such a degree as to be
negligable in the waste stream. Our institution generates 65,000 gallons
of waste water daily, which allows us to make the dilution limits of
anything that our histo lab could produce in a day. 

No laws are broken if I should pour xylene, formalin, alcohols or other
common compounds that we might generate on even our busiest days into
the waste stream. 

HOWEVER, while we may be allowed to do so by state and local
regulations, we have decided it is not prudent to do so and so we
collect, ship, neutralize or recycle most all that the histo lab
generates. We do this at the lab level, with lab funding. It is the
responsible thing to do, and we are morally and ethically bound to do
so, but we are not outside the law if we do not.

If your local municipal waste systems people give you the green light on
dumping formalin down the drain. you are not breaking the law,
federal or otherwise, in doing so. 

It is true that if you wish to affect things globally, one has to be
responsible locally.

Here is what my rant comes down to Make certain that you are meeting
local standards for your chemical disposal or you may well be breaking
the law. And a big thank you (from myself, my children, grandchildren
and great-grand children and that lady who sells me the slurpee at the
local convenience store) for anything anyone is doing above and beyond
that. 

:)Rant is over... Have a nice day :)  

You cannot Like this rant on Facebook or follow this rant on Twitter. 

Bill


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
mtitf...@aol.com
Sent: Monday, July 25, 2011 12:59 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Formalin down the drain??



I was a little distressed to read the message from Amy in Camp Hill,
Pennsylvania declaring she dumps everything (and I mean everything)
from her histology lab down the drain. There are a bunch of Federal Laws
governing handling and disposal of chemicals used in the histology
laboratory and she appears to be breaking several. The wastewater law
limits how much formalin you can discard down the sink (and you cannot
dilute as you go). The same law forbids disposal of organic solvents
like xylene, or solutions containing organic solvents. Local laws in
Pennsylvania may be more strict.

I recommend to Amy that she purchases a book like, Hazardous materials
in the histopathology laboratory by Janet  Richard Dapson and read the
whole thing cover to cover!

Michael Titford
Pathology USA
Mobile AL USA

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RE: [Histonet] Formalin down the drain??

2011-07-25 Thread Bea DeBrosse-Serra
I totally agree, under any circumstances, whatever the State law defines, we 
should not dump formalin, xylene or alcohols down the drain. And even though 
California has very strict rules, it even seems to differ from county to 
county. In one of my past jobs we were allowed to dump the formalin down the 
drain (Orange County of all places), whereas in San Diego, that was absolutely 
prohibited.

Beatrice DeBrosse-Serra HT(ASCP)QIHC
Isis Pharmaceuticals
Antisense Drug Discovery
1896 Rutherford Road
Carlsbad, CA 92008
760-603-2371




-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of O'Donnell, Bill
Sent: Monday, July 25, 2011 1:20 PM
To: mtitf...@aol.com; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Formalin down the drain??

One should not automtically assume that laws are broken here. 

(Rant begins here)

First of all, it is the States that set the limits of what can and
cannot be dumped. All States must meet Federal standards,but States are
free to determine how they do that. (It's one of the benefits of the
American Revolution) Some states are more heavily regulated than others.
California and Colorado come to mind immediately.

Different organizations, locations and circumstances may allow for
disposal of products that may be diluted to such a degree as to be
negligable in the waste stream. Our institution generates 65,000 gallons
of waste water daily, which allows us to make the dilution limits of
anything that our histo lab could produce in a day. 

No laws are broken if I should pour xylene, formalin, alcohols or other
common compounds that we might generate on even our busiest days into
the waste stream. 

HOWEVER, while we may be allowed to do so by state and local
regulations, we have decided it is not prudent to do so and so we
collect, ship, neutralize or recycle most all that the histo lab
generates. We do this at the lab level, with lab funding. It is the
responsible thing to do, and we are morally and ethically bound to do
so, but we are not outside the law if we do not.

If your local municipal waste systems people give you the green light on
dumping formalin down the drain. you are not breaking the law,
federal or otherwise, in doing so. 

It is true that if you wish to affect things globally, one has to be
responsible locally.

Here is what my rant comes down to Make certain that you are meeting
local standards for your chemical disposal or you may well be breaking
the law. And a big thank you (from myself, my children, grandchildren
and great-grand children and that lady who sells me the slurpee at the
local convenience store) for anything anyone is doing above and beyond
that. 

:)Rant is over... Have a nice day :)  

You cannot Like this rant on Facebook or follow this rant on Twitter. 

Bill


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
mtitf...@aol.com
Sent: Monday, July 25, 2011 12:59 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Formalin down the drain??



I was a little distressed to read the message from Amy in Camp Hill,
Pennsylvania declaring she dumps everything (and I mean everything)
from her histology lab down the drain. There are a bunch of Federal Laws
governing handling and disposal of chemicals used in the histology
laboratory and she appears to be breaking several. The wastewater law
limits how much formalin you can discard down the sink (and you cannot
dilute as you go). The same law forbids disposal of organic solvents
like xylene, or solutions containing organic solvents. Local laws in
Pennsylvania may be more strict.

I recommend to Amy that she purchases a book like, Hazardous materials
in the histopathology laboratory by Janet  Richard Dapson and read the
whole thing cover to cover!

Michael Titford
Pathology USA
Mobile AL USA

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RE: [Histonet] Where Can I Buy Pneumo Control Slides

2011-07-25 Thread Michele Wich
American MasterTech sells them:

http://www.americanmastertech.com/store/main.aspx?p=ItemDetailStylesite
m=CSP015P


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
wanda.sm...@hcahealthcare.com
Sent: Monday, July 25, 2011 3:26 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Where Can I Buy Pneumo Control Slides

Good Afternoon to All,
I am getting pretty desperate to find a source for Pneumo control
slides.  I know they are hard to come by, but my favorite source
Newcomer Supply does not have any and I ordered some from Sigma-Aldrich
and now they are discontinued.  Please Help!
Thanks,
Wanda

WANDA G. SMITH, HTL(ASCP)HT
Pathology Supervisor
TRIDENT MEDICAL CENTER
9330 Medical Plaza Drive
Charleston, SC  29406
843-847-4586
843-847-4296 fax


This email and any files transmitted with it may contain PRIVILEGED or
CONFIDENTIAL information and may be read or used only by the intended
recipient. If you are not the intended recipient of the email or any of
its attachments, please be advised that you have received this email in
error and that any use, dissemination, distribution, forwarding,
printing, or copying of this email or any attached files is strictly
prohibited. If you have received this email in error, please immediately
purge it and all attachments and notify the sender by reply email or
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RE: [Histonet] Formalin down the drain??

2011-07-25 Thread Galbraith, Joe
Indeed not only county to county but your local municipality can have specific 
regulations related to hazardous waste discard in the sewer since it is their 
waste treatment plant that takes the hit so to speak.  Most small 
municipalities will adopt state or county regulations (whichever is stricter) 
but they can always write even stricter rules if they wish and that may well be 
the case in some larger metro areas.  Good luck.  Joe University of Iowa

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Bea 
DeBrosse-Serra
Sent: Monday, July 25, 2011 3:56 PM
To: 'O'Donnell, Bill'; mtitf...@aol.com; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Formalin down the drain??

I totally agree, under any circumstances, whatever the State law defines, we 
should not dump formalin, xylene or alcohols down the drain. And even though 
California has very strict rules, it even seems to differ from county to 
county. In one of my past jobs we were allowed to dump the formalin down the 
drain (Orange County of all places), whereas in San Diego, that was absolutely 
prohibited.

Beatrice DeBrosse-Serra HT(ASCP)QIHC
Isis Pharmaceuticals
Antisense Drug Discovery
1896 Rutherford Road
Carlsbad, CA 92008
760-603-2371




-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of O'Donnell, Bill
Sent: Monday, July 25, 2011 1:20 PM
To: mtitf...@aol.com; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Formalin down the drain??

One should not automtically assume that laws are broken here.

(Rant begins here)

First of all, it is the States that set the limits of what can and
cannot be dumped. All States must meet Federal standards,but States are
free to determine how they do that. (It's one of the benefits of the
American Revolution) Some states are more heavily regulated than others.
California and Colorado come to mind immediately.

Different organizations, locations and circumstances may allow for
disposal of products that may be diluted to such a degree as to be
negligable in the waste stream. Our institution generates 65,000 gallons
of waste water daily, which allows us to make the dilution limits of
anything that our histo lab could produce in a day.

No laws are broken if I should pour xylene, formalin, alcohols or other
common compounds that we might generate on even our busiest days into
the waste stream.

HOWEVER, while we may be allowed to do so by state and local
regulations, we have decided it is not prudent to do so and so we
collect, ship, neutralize or recycle most all that the histo lab
generates. We do this at the lab level, with lab funding. It is the
responsible thing to do, and we are morally and ethically bound to do
so, but we are not outside the law if we do not.

If your local municipal waste systems people give you the green light on
dumping formalin down the drain. you are not breaking the law,
federal or otherwise, in doing so.

It is true that if you wish to affect things globally, one has to be
responsible locally.

Here is what my rant comes down to Make certain that you are meeting
local standards for your chemical disposal or you may well be breaking
the law. And a big thank you (from myself, my children, grandchildren
and great-grand children and that lady who sells me the slurpee at the
local convenience store) for anything anyone is doing above and beyond
that.

:)Rant is over... Have a nice day :)

You cannot Like this rant on Facebook or follow this rant on Twitter.

Bill


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
mtitf...@aol.com
Sent: Monday, July 25, 2011 12:59 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Formalin down the drain??



I was a little distressed to read the message from Amy in Camp Hill,
Pennsylvania declaring she dumps everything (and I mean everything)
from her histology lab down the drain. There are a bunch of Federal Laws
governing handling and disposal of chemicals used in the histology
laboratory and she appears to be breaking several. The wastewater law
limits how much formalin you can discard down the sink (and you cannot
dilute as you go). The same law forbids disposal of organic solvents
like xylene, or solutions containing organic solvents. Local laws in
Pennsylvania may be more strict.

I recommend to Amy that she purchases a book like, Hazardous materials
in the histopathology laboratory by Janet  Richard Dapson and read the
whole thing cover to cover!

Michael Titford
Pathology USA
Mobile AL USA

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[Histonet] RE: Histonet Digest, Vol 92, Issue 33

2011-07-25 Thread Joanne Clark


This sounds to me like a processing issue, especially with the types of tissues 
you describe.  Are the tissue sections you are referring to very thick?  Maybe 
the tissue is too big for the amount of time in the different processing 
stations.  I have also seen this happen when the tissue has been left to dry 
out before the clinician puts it into the formalin.

Joanne Clark, HT
Histology Supervisor
Pathology Consultants of New Mexico

--

Message: 2
Date: Mon, 25 Jul 2011 13:42:25 -0400
From: Carol Bryant cb...@lexclin.com
Subject: [Histonet] blurry tissue 
To: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Message-ID: 50DA0C6B72976B4AB3A0FCA04CC73DBF141CC36F8E@EXCHANGESB
Content-Type: text/plain; charset=us-ascii

I would like some thoughts on how to resolve some blurry looking tissue.  We 
have had occasional tissue that looks blurry and not crisp for several weeks 
now.  It is not all the cases only random tissues.  The tissue is not on the 
same tissue processor either. We have 2 processors.  The latest cases were a 
breast, some skins, and a prostate.  I am not certain if this is happening on 
the tissue processor or in the stainer.  It has been very humid in our lab so I 
have started running a dehumidifier in case there is water in the xylene.  It 
is so hit and miss that I am puzzled.   Any suggestions would be greatly 
appreciated.
Thank you in advance for your thoughts.

Carol Bryant, CT (ASCP)
Cytology/Histology Manager
Pathology Services
Lexington Clinic
Phone (859) 258-4082
Fax (859) 258-4081
cb...@lexclin.com



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RE: [Histonet] Where Can I Buy Pneumo Control Slides

2011-07-25 Thread Laurie Colbert
American Master Tech.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
wanda.sm...@hcahealthcare.com
Sent: Monday, July 25, 2011 1:26 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Where Can I Buy Pneumo Control Slides

Good Afternoon to All,
I am getting pretty desperate to find a source for Pneumo control
slides.  I know they are hard to come by, but my favorite source
Newcomer Supply does not have any and I ordered some from Sigma-Aldrich
and now they are discontinued.  Please Help!
Thanks,
Wanda

WANDA G. SMITH, HTL(ASCP)HT
Pathology Supervisor
TRIDENT MEDICAL CENTER
9330 Medical Plaza Drive
Charleston, SC  29406
843-847-4586
843-847-4296 fax


This email and any files transmitted with it may contain PRIVILEGED or
CONFIDENTIAL information and may be read or used only by the intended
recipient. If you are not the intended recipient of the email or any of
its attachments, please be advised that you have received this email in
error and that any use, dissemination, distribution, forwarding,
printing, or copying of this email or any attached files is strictly
prohibited. If you have received this email in error, please immediately
purge it and all attachments and notify the sender by reply email or
contact the sender at the number listed.



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Re: [Histonet] Where Can I Buy Pneumo Control Slides

2011-07-25 Thread Debra Siena
Statlab sells pneumo controls and they are in human tissues. 

Thanks
Debbie Siena HT(ASCP)QIHC
Technical Manager | StatLab Medical Products
407 Interchange St. | McKinney, TX 75071
Direct: 972-436-1010  x229 | Fax: 972-436-1369
dsi...@statlab.com | www.statlab.com 


- Original Message -
From: Laurie Colbert [mailto:laurie.colb...@huntingtonhospital.com]
Sent: Monday, July 25, 2011 04:21 PM
To: wanda.sm...@hcahealthcare.com wanda.sm...@hcahealthcare.com; 
histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Where Can I Buy Pneumo Control Slides

American Master Tech.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
wanda.sm...@hcahealthcare.com
Sent: Monday, July 25, 2011 1:26 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Where Can I Buy Pneumo Control Slides

Good Afternoon to All,
I am getting pretty desperate to find a source for Pneumo control
slides.  I know they are hard to come by, but my favorite source
Newcomer Supply does not have any and I ordered some from Sigma-Aldrich
and now they are discontinued.  Please Help!
Thanks,
Wanda

WANDA G. SMITH, HTL(ASCP)HT
Pathology Supervisor
TRIDENT MEDICAL CENTER
9330 Medical Plaza Drive
Charleston, SC  29406
843-847-4586
843-847-4296 fax


This email and any files transmitted with it may contain PRIVILEGED or
CONFIDENTIAL information and may be read or used only by the intended
recipient. If you are not the intended recipient of the email or any of
its attachments, please be advised that you have received this email in
error and that any use, dissemination, distribution, forwarding,
printing, or copying of this email or any attached files is strictly
prohibited. If you have received this email in error, please immediately
purge it and all attachments and notify the sender by reply email or
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Re: [Histonet] HE protocol question

2011-07-25 Thread Tony Reilly
Hi Michelle
 
I have used both and my experience either is suitable for a good HE if they 
are used appropriately.  For regressive staining you just need to optimise the 
time of haematoxylin staining with the concentration and time of the 
differentiation step.
 
In a previous position I used Mayer's which is a progressive stain.  We stained 
for 4 minutes in our HE protocol however to get the best staining we gave it a 
whiff of differentiation (1 min with 0.025% Acid alcohol)  This was not to 
differentiate the nuclear staining but we found to get optimal nuclear staining 
the time required would result in some tissue types adopting a very pale blue 
haze in the background and removing this provided much better differential 
eosin staining.
 
For counterstaining special stains and IHC the Mayer's was by far the best I 
have used. 1 minute would provide delicate nuclear staining with a clear 
background.  This stain would not interfere with any other staining including 
nuclear staining for ER, PR, TTF1 etc.  Good bluing was achieved simply with a 
good wash in our quite basic tap water.
 
So I would recommend either for HE but progressive for a counterstain.
 
regards
Tony
 
 
 
 

Tony Reilly  B.App.Sc. , M.Sc.
Chief Scientist, Anatomical Pathology
Pathology Queensland-PA Laboratory
_
Clinical and Statewide Services Division| QueenslandHealth
 
Level 1, Building 15,Princess Alexandra Hospital
Ipswich Road,WOOLLOONGABBA  Qld4102
Ph: 07 3176 2412
Mob: 0402 139411
Fax: 07 3176 2930
Email: tony_rei...@health.qld.gov.au
Web:  www.health.qld.gov.au/qhcss/
 
 


 histot...@imagesbyhopper.com histot...@imagesbyhopper.com 7/25/2011 
 9:29 pm 
Hi Histonetters!

I'm looking for thoughts on preferences/pros/cons between using a progressive 
and a regressive HE on routine daily work.

Which hematoxylins do you prefer (commercially prepared), which eosin?

Anyone have a tried and true protocol for each method?

Thanks!

Michelle

Sent from my iPhone
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[Histonet] How hot is too hot for storing tissue blocks?

2011-07-25 Thread Hugh Luk

Hi folks,

We were hoping someone could recommend a temperature range acceptable for 
storing tissue blocks?  Also do you folks use a regular thermometer or a 
temperature chart recorder (records on graph) to record room temps?

We are going to move to a new location and need help with the fine details.

Thanks in advance,
Hugh
Hawaii
  
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[Histonet] (no subject)

2011-07-25 Thread Ruthie Wilson
Please unsubscribe me
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