RE: [Histonet] Wax removal

2010-07-16 Thread Wanda.Smith
We get our anti-fatigue mats from Lab Safety Supply.  They have an extra thick 
one that I highly recommend. 


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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-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tom Wells
Sent: Thursday, July 15, 2010 4:48 PM
To: Rathborne, Toni
Cc: histonet@lists.utsouthwestern.edu; Hartz, Rhonda SktnHR
Subject: RE: [Histonet] Wax removal


Hi Rhonda,

Where do you get the anti-fatigue mats Thanks. Tom

Tom Wells BSc, ART
Faculty
School of Medical Laboratory Sciences
British Columbia Institute of Technology Burnaby, BC Canada

-histonet-boun...@lists.utsouthwestern.edu wrote: -

To: Hartz, Rhonda  SktnHR rhonda.ha...@saskatoonhealthregion.ca,
histonet@lists.utsouthwestern.edu
From: Rathborne, Toni trathbo...@somerset-healthcare.com
Sent by: histonet-boun...@lists.utsouthwestern.edu
Date: 07/15/2010 10:04AM
Subject: RE: [Histonet] Wax removal

We have a paraffin scraper that our Housekeeping staff uses. It was purchased 
from   American MasterTech Scientific (item CPW04200E, and replacement blades 
item CPW04201P). We also have perforated anti-fatigue mats in aisles around the 
cutting stations which trap the wax and can be vacuumed/swept away when the mat 
is flipped.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu]on Behalf Of Hartz, Rhonda 
SktnHR
Sent: Thursday, July 15, 2010 12:42 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Wax removal


Hi everyone;

This may seem like a insignificant question, but we consistently have issues 
with injuries to our maintenance staff from cleaning the wax off of our floors. 
 Housekeeping has laid sticky layered mats all over our floors (like large 
mouse traps), which they peel off layer by layer as they become wax covered.  
Apparently these are very expensive.  Does anyone have any suggestions?

Rhonda Hartz
Technologist Supervisor
Anatomic Pathology Division
Saskatoon Health Region
(306) 655-8197
rhonda.ha...@saskatoonhealthregion.ca

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RE: [Histonet] Hemoglobin Stain

2010-07-16 Thread Anna Taylor

Hi Linda,


Thanks for the reply! No, I'm not limited to staining only. In fact, I will be 
performing some seperate IHC to demonstrate a couple of other proteins. It is 
simply my preference to use a histochemical technique for the following 
reasons. Firstly, from what I understand, staining will not be as laborious as 
IHC nor as difficult/technical to obtain positive results. Secondly, as this is 
part of my Honours year project, I would like to try my luck with several 
different techniques, and hemoglobin is the only molecule from the products I 
am looking at for which a simple histochemical approach is possible. Again, any 
suggestions would be highly valuable.


Cheers,
Anna

 Subject: RE: [Histonet] Hemoglobin Stain
 Date: Thu, 15 Jul 2010 11:41:54 -0500
 From: lseb...@uwhealth.org
 To: annatay...@hotmail.com; histonet@lists.utsouthwestern.edu
 
 Anna,
 
 Are you limited to histochemical stains?  Because if you're not,
 hemoglobin may be detected by immunohistochemistry quite nicely. 
 
 
 Linda A. Sebree
 University of Wisconsin Hospital  Clinics
 IHC/ISH Laboratory
 DB1-223 VAH
 600 Highland Ave.
 Madison, WI 53792
 (608)265-6596
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Anna
 Taylor
 Sent: Thursday, July 15, 2010 11:37 AM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Hemoglobin Stain
 
 
 Hi all,
 
 In my quest for advice about what will be my very first attempt at
 histology, I have been recommended to post my query here.
 
 I'm attempting to demonstrate hemoglobin in FFPE lymph node sections.
 I've been able to find a couple of techniques  (namely the Dunn 
 Thompson technique and Okajima's technique), although I'm not sure how
 suitable either would be on lymph node sections? As I said, this will be
 my debut experience in histology/histochemistry so any
 advice/recommendations at all will be appreciated :)Thanks,Anna.
 
 _
 View photos of singles in your area! Looking for a hot date?
 http://clk.atdmt.com/NMN/go/150855801/direct/01/
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[Histonet] Embedding multiple GI pieces on end in a paraffin block

2010-07-16 Thread kgrobert
Is there a way to do this without one or more pieces falling over?  I saw
in the archive the method for frozen sections-embed them on their sides in
OCT, then cut on the end, but I don't think I'd be able to do that in
paraffin.  Would one of the tissue microarray methods work?  (I've never
done that before, so I have no idea.)

Thanks in advance for all your help,
Kathleen


Principal Lab Technician
Neurotoxicology Labs
Molecular Pathology Facility Core
Dept of Pharmacology  Toxicology
Rutgers, the State University of NJ
41 B Gordon Road
Piscataway, NJ 08854
(732) 445-6914

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RE: [Histonet] Embedding multiple GI pieces on end in a paraffin block

2010-07-16 Thread sgoebel

   How many are we talking about?  I embed 6 sections of mouse = bowel on
   end and it works?  Just fill the mold, put it on the cold spo= t for a
   second, then on some room temperature area, the paraffin will harde= n
   slowly enough that you should be able to embed them?

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

   Histotechnician

   = /div
   XBiotech USA Inc.
   8201 East Riverside Dr. Bldg 4 Suite 100
  Austin, T= exas  78744
   (512)386-5107
   = br

    Original Message 
   Subject: [Histonet] Embedding multiple GI pieces on end in a paraffin
   block
   From: [1]kgrob...@rci.rutgers.ed= u
   Date: Fri, July 16, 2010 8:23 am
   To: histonet [2]h= isto...@lists.utsouthwestern.edu
   Is  there  a way to do this without one or more pieces falling over? I
   saw  in the archive the method for frozen sections-embed them on their
   sides in= br OCT, then cut on the end, but I don't think I'd be able
   to do that in
   paraffin. Would one of the tissue microarray methods work? (I've never
   done that before, so I have no idea.)
   Thanks in advance for all your help,
   Kathleen
   Principal Lab Technician
   Neurotoxicology Labs
   Molecular Pathology Facility Core
   Dept of Pharmacology  Toxicology
   Rutgers, the State University of NJ
   41 B Gordon Road
   Piscataway, NJ 08854
   (732) 445-6914
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References

   1. 3Dmailto://kgrob...@rci.rutgers.edu/
   2. 3Dmailto://histonet@lists.utsouthwestern.edu/
   3. 3Dmailto://Histonet@lists.utsouthwestern.edu/
   4. 3Dhttp://lists.utsouthwestern.edu/mailman/listinfo/histonet;
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RE: [Histonet] Embedding multiple GI pieces on end in a paraffin block

2010-07-16 Thread Mike Pence
I have techs that embed 10-15 pieces on end in one block. Just cool the
block slowly and move your pieces around quickly.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
kgrob...@rci.rutgers.edu
Sent: Friday, July 16, 2010 10:24 AM
To: histonet
Subject: [Histonet] Embedding multiple GI pieces on end in a paraffin
block


Is there a way to do this without one or more pieces falling over?  I
saw in the archive the method for frozen sections-embed them on their
sides in OCT, then cut on the end, but I don't think I'd be able to do
that in paraffin.  Would one of the tissue microarray methods work?
(I've never done that before, so I have no idea.)

Thanks in advance for all your help,
Kathleen


Principal Lab Technician
Neurotoxicology Labs
Molecular Pathology Facility Core
Dept of Pharmacology  Toxicology
Rutgers, the State University of NJ
41 B Gordon Road
Piscataway, NJ 08854
(732) 445-6914

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[Histonet] Paraffin Block Storage

2010-07-16 Thread Andrew Burgeson
Hello histonetters,

Does anyone know of a good source of used or economical
plastic storage drawer cabinets for paraffin blocks?
Auctions, used equipment, or otherwise retailers?
Interested in purchasing some. We have thousands of blocks
to store.

Thanks!

AB

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Re: [Histonet] Embedding multiple GI pieces on end in a paraffin block

2010-07-16 Thread Drew Meyer
We regularly embed 6-12 pieces on end in one block without any special
method.  You just have to be quick... and don't leave the block on the cold
plate very long... just touch the cold plate briefly while embedding the
individual piece, then lift the block off the plate until you grab the next
piece... repeat quickly and you'll run out of room in the mold before you'll
have to worry about it hardening too much.

Drew

On Fri, Jul 16, 2010 at 11:23, kgrob...@rci.rutgers.edu wrote:

 Is there a way to do this without one or more pieces falling over?  I saw
 in the archive the method for frozen sections-embed them on their sides in
 OCT, then cut on the end, but I don't think I'd be able to do that in
 paraffin.  Would one of the tissue microarray methods work?  (I've never
 done that before, so I have no idea.)

 Thanks in advance for all your help,
 Kathleen


 Principal Lab Technician
 Neurotoxicology Labs
 Molecular Pathology Facility Core
 Dept of Pharmacology  Toxicology
 Rutgers, the State University of NJ
 41 B Gordon Road
 Piscataway, NJ 08854
 (732) 445-6914

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RE: [Histonet] Paraffin Block Storage

2010-07-16 Thread Bell, Lynne
In Vermont we are very frugal.  What I have used for more years than I care to 
remember are pizza boxes from Pizza Hut.  Our local Pizza Hut gives them to us 
for free.  They are very sturdy and perfectly fit 11 rows across and 
approximately 36 blocks per row.  I have 20 years of blocks stored this way.

Lynne A. Bell, HT (ASCP)
Technical Specialist, Histology
Central Vermont Medical Center
130 Fisher Road
Barre, VT  05641
802-371-4923


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[Histonet] Lab in Aiken, South Carolina seeking histotech

2010-07-16 Thread Brian- Prometheus
 

Outpatient laboratory located in Aiken South Carolina is currently seeking a
histotech.  

The company includes 20 specialty pathologists, more than 100 dedicated
professionals, operates 9 patient service centers, and provides medical
directorship for 18 hospitals throughout Georgia and northern Florida.

 

Please contact me today for consideration

 

Brian Feldman

Principal

Prometheus Healthcare 

Office 301-693-9057

Fax 301-368-2478

br...@prometheushealthcare.com mailto:br...@prometheushealthcare.com 

www.prometheushealthcare.com http://www.prometheushealthcare.com/ 

*** Stay up to date on the newest positions and healthcare trends nationwide
on Twitter!***

 http://twitter.com/PrometheusBlog

 

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RE: [Histonet] Embedding multiple GI pieces on end in a paraffin block

2010-07-16 Thread kgrobert
To all,

OK, looks like most of you are saying the same thing-work fast!  :o)  I've
printed out all of your replies and discussed them with the graduate
student who needs this done for her thesis, and she agrees with me-it's
just going to take practice.  I'll try the cool slowly/work fast
suggestions first and see how that goes, then see about the trick with the
cucumber (which sounds really cool!), slowly edging the mold onto the cold
plate as I go, and using sponges to help flip the samples on end (and not
necessarily in that order).  I don't want to try too many things at once,
lest I drive myself nuts.

The first batch of samples should be coming sometime next week.  Wish me
luck, and thanks for all your help!

Kathy



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RE: [Histonet] inking dyes

2010-07-16 Thread Cynthia Pyse
I use tattoo dyes. They work great and are much cheaper than tissue marking
dyes.
Cindy Pyse, CLT, HT (ASCP)
Histology Supervisor
X-Cell Laboratories
e-mail cp...@x-celllab.com



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Diana McCaig
Sent: Thursday, July 15, 2010 10:53 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] inking dyes

Can someone provide me with a supplier of tissue marking dyes for use on
the grossing bench.
 
Diana McCaig
Histology Lab
Chatham Kent Health Alliance
80 Grand Avenue West
Chatham. Ontario
N7L 1B7
519-352-6401  (6604)
 
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of the intended recipient only. Any review, retransmission or
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recipient is prohibited. If you receive this email in error, please
contact the sender and delete this communication and any copies
immediately. Thank you. 
 
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[Histonet] Re: NG2 antibody/ Antigen retrieval/Protocol

2010-07-16 Thread Hobbs, Carl
I am trying to stain human glioma sections(as a positive control) using 
Anti-NG2 antibody. The tissue that I have is Paraffin embedded and I appreciate 
if somebody could send me the protocol for antigen retrieval ,antibody titer 
and IHC protocol. 

Let us know what Ab you are currently using ( Source and catalogue number) and 
also what detection/AR  protocol you are using.
Also, what problem do you have using your Ab?
Best wishes,
Carl


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[Histonet] Cytology 100 slide limit

2010-07-16 Thread Victor Tobias
 Our Cytology Supervisor was telling me about the 100 slide maximum 
that they can screen in a day. Our LIS is not capturing the NON-GYN 
slides being screened, so unless you are very diligent in recording the 
slides screened, you could go over the 100 limit.


Our supervisor also believes the computer system should notify the user 
when the limit has been reached and prevent them from continuing. Is 
this a CAP requirement? How are you dealing with this problem or is it a 
problem for you?


Victor

--
Victor Tobias
Clinical Applications Analyst
University of Washington Medical Center
Dept of Pathology Room BB220
1959 NE Pacific
Seattle, WA 98195
vic...@pathology.washington.edu
206-598-2792
206-598-7659 Fax
=
Privileged, confidential or patient identifiable information may be
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of the intended recipients. If you are not the intended recipient, or
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transmission. Instead, please notify the sender by reply e-mail, and
then destroy all copies of the message and any attachments.


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Re: [Histonet] Cytology 100 slide limit

2010-07-16 Thread Rene J Buesa

Victor:
As you wrote, either you have to be diligent in recording your work, or you 
will have to modify the software of the LIS system to account correctly.
On the other hand, if you are dealing with liquid base samples usually using a 
Thin-Prep Imaging System (TIS) and the sample covers one-half or less of the 
slide surface, CLIA88 has expanded the limit from 100 to 200 slides/day.
René J.

--- On Fri, 7/16/10, Victor Tobias vic...@pathology.washington.edu wrote:


From: Victor Tobias vic...@pathology.washington.edu
Subject: [Histonet] Cytology 100 slide limit
To: Histonet Histonet@lists.utsouthwestern.edu
Date: Friday, July 16, 2010, 3:33 PM


Our Cytology Supervisor was telling me about the 100 slide maximum that they 
can screen in a day. Our LIS is not capturing the NON-GYN slides being 
screened, so unless you are very diligent in recording the slides screened, you 
could go over the 100 limit.

Our supervisor also believes the computer system should notify the user when 
the limit has been reached and prevent them from continuing. Is this a CAP 
requirement? How are you dealing with this problem or is it a problem for you?

Victor

-- Victor Tobias
Clinical Applications Analyst
University of Washington Medical Center
Dept of Pathology Room BB220
1959 NE Pacific
Seattle, WA 98195
vic...@pathology.washington.edu
206-598-2792
206-598-7659 Fax
=
Privileged, confidential or patient identifiable information may be
contained in this message. This information is meant only for the use
of the intended recipients. If you are not the intended recipient, or
if the message has been addressed to you in error, do not read,
disclose, reproduce, distribute, disseminate or otherwise use this
transmission. Instead, please notify the sender by reply e-mail, and
then destroy all copies of the message and any attachments.


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[Histonet] New Job Opportunities

2010-07-16 Thread Jan . Minshew

Hello everyone and happy Friday to all,

Leica Microsystems is adding new positions and would like to hear from
those of you who might be interested.  The positions are for Field Support
Specialists (FSS) and will be based in the following areas:

Southeast Florida
NYC/Bronx/NJ
MD/VA/DC
TN/MS/AR
NM/TX/western OK
CO/WY/MT
Southern IL/Iowa

Some of the responsibilities include in-field support for IHC, conducting
demonstrations and post-sales customer training, performing validations and
optimization, and providing technical support for remote problem solving.

If you are interested in trying something different and feel that you are
qualified, please contact Linda Jordan, HR Recruiter at
hrco...@leica-microsystems.com.

Kind regards,

Jan Minshew
Marketing Manager
Leica Microsystems
Biosystems Division
2345 Waukegan Road
Bannockburn, IL 60015

Office:  847.405.7051
Cell: 847.970.8468
Fax: 847.405.6560

www.leica-microsystems.com


Click Here for this month's special offers!
http://www.leica-microsystems.com/bsdspecial


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RE: [Histonet] Cytology 100 slide limit

2010-07-16 Thread Feher, Stephen
Victor,

Rene is correct in stating that CLIA allows Gyn Liquid Based Paps to be counted 
as 1/2 slide.  It gets tricky when you start mixing 1/2 slide counts and full 
slide counts in making sure the techs do not exceed 100 slides (or in the case 
of LBP's 200 slides).  If you get a lot of FNA's the counts can go up very 
quickly.

Most LIS systems can prevent Techs from exceeding their limit.  I would check 
again to see why your LIS is not capturing the NON-Gyn slides.  Another CAP and 
CLIA requirement is that each 6 months, the cytotechs are supposed to have a 
Competency Assessment where the Medical Director signs off on the maximum 
number of slides each tech is qualified to screen.  This is the number that 
most labs place in the LIS as the max that particular tech can review.

What LIS system do you have? 


Steve

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rene J Buesa
Sent: Friday, July 16, 2010 5:21 PM
To: Histonet; Victor Tobias
Subject: Re: [Histonet] Cytology 100 slide limit


Victor:
As you wrote, either you have to be diligent in recording your work, or you 
will have to modify the software of the LIS system to account correctly.
On the other hand, if you are dealing with liquid base samples usually using a 
Thin-Prep Imaging System (TIS) and the sample covers one-half or less of the 
slide surface, CLIA88 has expanded the limit from 100 to 200 slides/day.
René J.

--- On Fri, 7/16/10, Victor Tobias vic...@pathology.washington.edu wrote:


From: Victor Tobias vic...@pathology.washington.edu
Subject: [Histonet] Cytology 100 slide limit
To: Histonet Histonet@lists.utsouthwestern.edu
Date: Friday, July 16, 2010, 3:33 PM


Our Cytology Supervisor was telling me about the 100 slide maximum that they 
can screen in a day. Our LIS is not capturing the NON-GYN slides being 
screened, so unless you are very diligent in recording the slides screened, you 
could go over the 100 limit.

Our supervisor also believes the computer system should notify the user when 
the limit has been reached and prevent them from continuing. Is this a CAP 
requirement? How are you dealing with this problem or is it a problem for you?

Victor

-- Victor Tobias
Clinical Applications Analyst
University of Washington Medical Center
Dept of Pathology Room BB220
1959 NE Pacific
Seattle, WA 98195
vic...@pathology.washington.edu
206-598-2792
206-598-7659 Fax
=
Privileged, confidential or patient identifiable information may be contained 
in this message. This information is meant only for the use of the intended 
recipients. If you are not the intended recipient, or if the message has been 
addressed to you in error, do not read, disclose, reproduce, distribute, 
disseminate or otherwise use this transmission. Instead, please notify the 
sender by reply e-mail, and then destroy all copies of the message and any 
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RE: [Histonet] Embedding multiple GI pieces on end in a paraffin block

2010-07-16 Thread R J VAZQUEZ

Hello,

The way I used to embed GI specimens is to place them on end on a stack of 
specimen bags that have solidified, since they are already in place, then you 
can pick them up quickly. I did this with sectioned arterial artieries or vas 
deferens this worked like a dream.

 

Robyn Vazquez
 
 Date: Fri, 16 Jul 2010 11:00:01 -0500
 From: mpe...@grhs.net
 To: kgrob...@rci.rutgers.edu; histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] Embedding multiple GI pieces on end in a paraffin 
 block
 CC: 
 
 I have techs that embed 10-15 pieces on end in one block. Just cool the
 block slowly and move your pieces around quickly.
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
 kgrob...@rci.rutgers.edu
 Sent: Friday, July 16, 2010 10:24 AM
 To: histonet
 Subject: [Histonet] Embedding multiple GI pieces on end in a paraffin
 block
 
 
 Is there a way to do this without one or more pieces falling over? I
 saw in the archive the method for frozen sections-embed them on their
 sides in OCT, then cut on the end, but I don't think I'd be able to do
 that in paraffin. Would one of the tissue microarray methods work?
 (I've never done that before, so I have no idea.)
 
 Thanks in advance for all your help,
 Kathleen
 
 
 Principal Lab Technician
 Neurotoxicology Labs
 Molecular Pathology Facility Core
 Dept of Pharmacology  Toxicology
 Rutgers, the State University of NJ
 41 B Gordon Road
 Piscataway, NJ 08854
 (732) 445-6914
 
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 Histonet mailing list
 Histonet@lists.utsouthwestern.edu
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[Histonet] Wax removal

2010-07-16 Thread Amos Brooks
Hi,
 You can get abrasive pads that have adhesive on one side. They are
usually used on stairs. They are like 8 inch wide 3 foot long strips of
sandpaper that stick (really well) to the floor. I have them placed about 1
per foot along main traffic areas. I don't recall off the top of my head
where we got them from, but if you'd like, I'll look it up on Monday.

Amos


Message: 6
Date: Thu, 15 Jul 2010 10:42:26 -0600
From: Hartz, Rhonda  SktnHR rhonda.ha...@saskatoonhealthregion.ca
Subject: [Histonet] Wax removal
To: histonet@lists.utsouthwestern.edu
Message-ID: b7f15445a710ba4fa7b48f2c55134ad404b3d...@lou.sktnhr.ca
Content-Type: text/plain;   charset=US-ASCII

Hi everyone;

This may seem like a insignificant question, but we consistently have
issues with injuries to our maintenance staff from cleaning the wax off
of our floors.  Housekeeping has laid sticky layered mats all over our
floors (like large mouse traps), which they peel off layer by layer as
they become wax covered.  Apparently these are very expensive.  Does
anyone have any suggestions?

Rhonda Hartz
Technologist Supervisor
Anatomic Pathology Division
Saskatoon Health Region
(306) 655-8197
rhonda.ha...@saskatoonhealthregion.ca
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RE: [Histonet] Wax removal

2010-07-16 Thread connie grubaugh

We get our anti-fatigue mats from Sam's make sure you get the red ones and not 
the black ones. They are in the office materials area.



Connie G.



 

 From: wanda.sm...@hcahealthcare.com
 To: tom_we...@bcit.ca; trathbo...@somerset-healthcare.com
 Date: Fri, 16 Jul 2010 09:00:01 -0500
 Subject: RE: [Histonet] Wax removal
 CC: histonet@lists.utsouthwestern.edu; rhonda.ha...@saskatoonhealthregion.ca
 
 We get our anti-fatigue mats from Lab Safety Supply. They have an extra thick 
 one that I highly recommend. 
 
 
 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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 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tom Wells
 Sent: Thursday, July 15, 2010 4:48 PM
 To: Rathborne, Toni
 Cc: histonet@lists.utsouthwestern.edu; Hartz, Rhonda SktnHR
 Subject: RE: [Histonet] Wax removal
 
 
 Hi Rhonda,
 
 Where do you get the anti-fatigue mats Thanks. Tom
 
 Tom Wells BSc, ART
 Faculty
 School of Medical Laboratory Sciences
 British Columbia Institute of Technology Burnaby, BC Canada
 
 -histonet-boun...@lists.utsouthwestern.edu wrote: -
 
 To: Hartz, Rhonda SktnHR rhonda.ha...@saskatoonhealthregion.ca,
 histonet@lists.utsouthwestern.edu
 From: Rathborne, Toni trathbo...@somerset-healthcare.com
 Sent by: histonet-boun...@lists.utsouthwestern.edu
 Date: 07/15/2010 10:04AM
 Subject: RE: [Histonet] Wax removal
 
 We have a paraffin scraper that our Housekeeping staff uses. It was purchased 
 from   American MasterTech Scientific (item CPW04200E, and replacement blades 
 item CPW04201P). We also have perforated anti-fatigue mats in aisles around 
 the cutting stations which trap the wax and can be vacuumed/swept away when 
 the mat is flipped.
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu]on Behalf Of Hartz, Rhonda 
 SktnHR
 Sent: Thursday, July 15, 2010 12:42 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Wax removal
 
 
 Hi everyone;
 
 This may seem like a insignificant question, but we consistently have issues 
 with injuries to our maintenance staff from cleaning the wax off of our 
 floors.  Housekeeping has laid sticky layered mats all over our floors (like 
 large mouse traps), which they peel off layer by layer as they become wax 
 covered.  Apparently these are very expensive.  Does anyone have any 
 suggestions?
 
 Rhonda Hartz
 Technologist Supervisor
 Anatomic Pathology Division
 Saskatoon Health Region
 (306) 655-8197
 rhonda.ha...@saskatoonhealthregion.ca
 
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