RE: [Histonet] Peloris Users

2010-07-08 Thread Josie Britton
 

We have helped that problem by being sure there is adequate graded
alcohols on the Peloris.  There must be between 60-70%, 80-90%, and 95%
before you have the 100% alcohols.  If the concentration's are too high
there is inadequate infiltration of the tissue's.  We usually only use
the 2 hour and the 8 hour processing factory default.  Unless, we have a
stat.  We have also noticed if you wait until Prompted to change the
lowest alcohol at 51% we see degradation in our staining as well.  We
are not letting it get below 58-60% before we change an alcohol out.  

 

I hope this helps,

 

Josie Britton HT

Cheshire Medical Center

580 Court Street

Keene, NH 03431

603-354-5454 ext.2454

 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Sharon.Davis-Devine
Sent: Thursday, July 08, 2010 9:51 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Peloris Users

 

To all you Peloris users, here is my delimma.  When we follow the
machines prompt to change the solutions because of purity and we then
process small biopsies on the machine, it overprocesses the specimens.
So the staff have been overrriding the prompt to change the solutions
causing specimens to be processed in impure solutions causing a host of
other problems. Have any of you out there with Peloris experience had
this problem? Is it a machine problem that should be fixed or human
error due to overriding the prompts?  I am new to this position and have
very little experience with this issue so any help or suggestions will
be greatly appreiciated. Thank you.

 

Sharon Davis-Devine, CT (ASCP)

Cytology-Histology  Supervisor

Carle Foundation Hospital

Laboratory and Pathology Services

611 West Park Street

Urbana, Illinois 61801

217-383-3572

sharon.davis-dev...@carle.com

 

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RE: [Histonet] (no subject)

2010-06-25 Thread Josie Britton
 

We retain our containers and specimens for 3 weeks.

 

Josie

 

 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Feher,
Stephen
Sent: Wednesday, June 23, 2010 5:51 PM
To: Hartz, Rhonda SktnHR; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] (no subject)

 

We retain them until the specimen is signed out, usually no more than 3

days.  This has been helpful if the specimen container labeling is

called into question either by the pathologist (because the cellular

profile does not match what the specimen source indicates) or the

clinician. 

 

 

Steve

 

-Original Message-

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

[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Hartz,

Rhonda SktnHR

Sent: Tuesday, June 22, 2010 5:55 PM

To: histonet@lists.utsouthwestern.edu

Subject: [Histonet] (no subject)

 

Hi.  This is my first time, so I apologize if I am not clear enough.  We

have had a request from one of our pathologists to retain empty specimen

containers after grossing is complete.  Is anyone aware of any

recommendations, or does anyone out there retain their empty specimen

containers?

 

Rhonda Hartz

Technologist Supervisor

Anatomic Pathology Division

Saskatoon Health Region

(306) 655-8197

rhonda.ha...@saskatoonhealthregion.ca

 

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RE: [Histonet] slim jims

2010-06-23 Thread Josie Britton
We put them in the formalin first just like a specimen.

 

Josie

 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Perry,
Margaret
Sent: Tuesday, June 22, 2010 2:48 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] slim jims

 

Do you put the slim jims in formalin and then process them or just put
them in the processor?

Margaret

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RE: [Histonet] Help! In need of positive Gram Control

2010-06-23 Thread Josie Britton
It's true!  Who knew that Gram + and- riddles meat sticks could be so
yummy and versatile too! 

 

Josie

 

-Original Message-
From: Gill, Caula A. [mailto:cg...@marylandgeneral.org] 
Sent: Tuesday, June 22, 2010 10:16 AM
To: Josie Britton; dianar...@aol.com; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Help! In need of positive Gram Control

 

You have got to be kidding!! That's hysterical. So process a slim jim

and you have 

Gram - and + controls. If you're serious I'm trying it. 

 

-Original Message-

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

[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Josie

Britton

Sent: Tuesday, June 22, 2010 6:10 AM

To: dianar...@aol.com; histonet@lists.utsouthwestern.edu

Subject: RE: [Histonet] Help! In need of positive Gram Control

 

 

 

 

 

Have you tried a Slim Jim?  They have gram positive and negative rods in

 

them.  Regardless, I still enjoy eating them once and a while! 

 

 

 

 

 

 

 

Josie Britton Ht

 

 

 

Cheshire Medical Center

 

 

 

Keene, NH 03431

 

 

 

 

 

 

 

 

 

 

 

-Original Message-

 

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

 

[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of

 

dianar...@aol.com

 

Sent: Monday, June 21, 2010 7:43 PM

 

To: histonet@lists.utsouthwestern.edu

 

Subject: [Histonet] Help! In need of positive Gram Control

 

 

 

 

 

 

 

Help! We are in need of positive Gram Control Blocks if anyone has any  

 

 

 

extra they are willing to part with.  I have lots of Fungus,

 

Pneumocystis  and 

 

 

 

HPV tissue blocks to trade.

 

 

 

 

 

 

 

Diana Ripley

 

 

 

John Muir Histology

 

 

 

Concord Campus

 

 

 

2540 East Street

 

 

 

Concord, CA 94520

 

 

 

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[Histonet] Breezy lab/flyaway ribbons!

2010-06-22 Thread Josie Britton
We have been having trouble with big breeze blowing our precious ribbons
out of our hands while cutting.  We would like a door on the Histology
lab to cut down on the breeze of people walking by through the hall.
Our facilities want to find out what other people are doing to stop this
problem.  We also have air ducts blowing down from above, which is not
helping the problem.  We would like as many labs solutions as possible.
Our facilities have come up with all these crazy barriers that we would
have to move to walk around when we need to put our racks on the
stainer, answer timers, print more slides, use the oven, etc... 

 

Any input would be appreciated!

 

Breezy girls,

 

Josie Britton and Chris Braaten

Cheshire Medical Center

Keene, NH 03431


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RE: [Histonet] RE: AMT Cover

2010-05-14 Thread Josie Britton
 

I second that!

 

Josie Britton HT

Keene, NH

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Dawson,
Glen
Sent: Friday, May 14, 2010 11:54 AM
To: histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] RE: AMT Cover

 

All,

 

I just looked at the notorious AMT cover that people are up in arms
about and I must disagree with the comments that were posted thus far.
The techs here and myself are quite surprised by the reactions because
it is on a medical catalogue and is far from being lewd or obscene.
You could probably find worse by turning on the TV for 15 minutes or
looking at a billboard or two.  

 

Just Some Wisconsin Input,

 

Glen Dawson  BS, HT  QIHC (ASCP)

IHC Manager

Milwaukee, WI

 

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RE: [Histonet] Xylene Recycler

2010-02-11 Thread Josie Britton
We resolved this issue by placing a filter/screen in our waste to be
recycled carboy.  After you clean out the excess lint and Schmutz from
the line you should be all set!

 

Welcome!

 

Josie Britton HT 

Cheshire Medical Center 

580 Court Street

Keene, NH 03431

603-354-5454 ext.2454

 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Nita
Searcy
Sent: Wednesday, February 10, 2010 12:58 PM
To: histonet@lists.utsouthwestern.edu
Cc: Patricia Webster
Subject: [Histonet] Xylene Recycler

 

Anyone using the new CBG instrument? Am having some issues with clogged
lines - which we never had with the older model. Really don't want to
change processes - which is what they are asking us to do.

 

Thanks

Nita 

 

Nita Searcy, HT/HTL (ASCP)

Scott and White Hospital

Division Manager, Anatomic Pathology

2401 S. 31st. Street 

254-724-2438

Temple, Texas, 76502

nsea...@swmail.sw.org

 

 

254-724-2438

 


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RE: [Histonet] EBER ISH problems

2010-01-20 Thread Josie Britton
Try switching your DAB kit to Refined Red, this helped us.  We also run
a negative RNA and positive RNA on the patient also.

 

Josie Britton HT

Cheshire Medical Center

Keene, NH

 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Goodacre, Suzanne
Sent: Wednesday, January 20, 2010 11:20 AM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] EBER ISH problems

 

Hello,

Our Histo lab currently uses the Leica Microsystems Bond
instrument for EBER ISH.  We noticed that eosinophils readily pick up
the DAB detection reagents that we use.  I've attempted to alter the
EBER ISH protocol on the BOND so that the eosinophils don't take on the
detection reagents but I'm not having much luck.  Does anyone have any
tips on how to prevent or avoid the problem?

 

Suzanne Goodacre

Research Technologist

Micro Molecular Lab

Children's Hospital of Wisconsin

414-266-2709

 

 

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RE: [Histonet] fish scales

2009-12-11 Thread Josie Britton
Nair hair remover works great on toenails!

 

Josie Britton HT

 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Perry,
Margaret
Sent: Thursday, December 10, 2009 3:32 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] fish scales

 

We are trying to cut fish scales that have been decalcified.  They are
chunking out when we try to cut them.  I think we need to soften the
keratin and I looked in the archives for the right dilution of ammonium
hydroxide to use.  One post said 5% the other said straight.  What
dilution do you recommend?  I'm think it would probably be the same as
what you use on toenails.

 

Margaret Perry HT(ASCP)

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[Histonet] IHC Patient Negatives

2009-10-28 Thread Josie Britton
Hi All,

 

I have an issue with my computer, so I cannot see past the little
paragraphs on the Histonet archives.  Sorry!  This question is probably
asked many, many times.

 

When we run our IHC's we always have a patient negative slide to go with
our case.  We run everything accept Herceptin on the Bond. When running
a patient's IHC on the bench and on the Bond we use a negative patient
control for both.  (We run a test control on all antibodies also)  If we
are running a double stain IHC also we run another negative patient
control for that stain also.  The debate we are having is, if the next
day you run another IHC on the same patient using the same DAB define
kit, should we be running another negative patient control? 

 

Thanks for your help!

 

Josie Britton HT

Cheshire Medical Center

 


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RE: [Histonet] IHC Zinc Fixative supplier/source

2009-10-15 Thread Josie Britton
We use Z-Fix from Anatech LTD, 269-964-6450.

 

Josie Britton HT

 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cormier,
Kathleen
Sent: Thursday, October 15, 2009 8:24 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] IHC Zinc Fixative supplier/source

 

Hello Netters,

 

 

 

I am searching for a vendor to supply IHC Zinc fixative. Not zinc

formalin. It's ALMOST like the BD Pharmingen IHC zinc fix, but contains

Zinc acetate too. We do not want to make it up in house thoughit

contains calcium acetate, zinc acetate, zinc chloride and tris buffer. I

have searched the 'net and all I garnered was a head ache, there are so

many variations of zinc fixatives, and none are what we need. Any help

would be appreciated. Thank you!

 

 

 

Kathy Cormier

 

Histology Manager

 

Charles River Laboratories

 

251 Ballardvale Street 

 

Wilmington, MA 01887

 

Ph: 781-222-6803

 

Fax: 978-988-8793

 

kathleen.corm...@crl.com BLOCKED::mailto:kathleen.corm...@crl.com 

 

 

 

Experience the new www.criver.com http://www.criver.com/  

 

 

 

Accelerating Drug Development. Exactly.

 

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RE: [Histonet] Leica Bond/Novocastra Reagents

2009-10-05 Thread Josie Britton
 

We get almost all their antibodies and ancillaries and have never had a
problem!  They are a great company and we love the Bond Max.

 

Josie Britton HT

Cheshire Medical Center

Keene, NH 03431

 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Paula
Lucas
Sent: Monday, October 05, 2009 11:20 AM
To: histo...@pathology.swmed.edu
Subject: [Histonet] Leica Bond/Novocastra Reagents

 

Hello,

 

We are considering the Leica Bond and their reagent rental or
acquisition option, and I have a question regarding back orders.  

 

If anyone places an order through Leica for their Bond reagents
(novocastra), are there any problems with back orders on antibodies,
detection system and other reagents needed to run the Bond?  Or, do you
usually get the items right away?

 

Thank you,

Paula Lucas

Lab Manager

Bio-Path Medical Group

Fountain Valley, CA

 

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RE: [Histonet] water on slides?

2009-08-24 Thread Josie Britton
When this happens in our lab, we put Drierite (anhydrous calcium
sulfate) into the clearing agents.  Just put enough to have not quite a
solid layer on the bottom of the staining well, so it will not block the
staining rack from going all the way into the clearing agent.  We get
ours from W.A. Hammond Drierite Company LTD, Xenia, Ohio 45385.
Telephone number 937-376-2927.  I hope this helps!

 

Josie Britton HT

Cheshire Medical Center

Keene, NH 03431

 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Hayes,
Tina J.
Sent: Monday, August 24, 2009 12:41 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] water on slides?

 

We are having a problem with what seems to be water on our slides.  We

have had very high humidity levels in the air.  It seems that we look at

the slides before taking them to the pathology office, one pathologist

reviews them and sees little or no water droplets, but as they sit and

another pathologist reads them later, like the following day, the

droplets are very apparent.

 

 

 

We use Clearite-3.  We have no xylene in our lab.  We also coverslip

with Permount.

 

 

 

Is it possible that the clearite-3 and/or Permount is absorbing moisture

from the atmosphere to the slides?

 

And if so, do you have any suggestions for combating this issue?

 

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RE: [Histonet] LYVE-1 antibody

2009-08-12 Thread Josie Britton
 

We have one and we love it!  Our Pathologists keep adding more and more
antibodies to our list.  It is so easy to program.  Leica's support
staff are great too!

 

Josie Britton HT

Cheshire Medical Center 

Keene, NH 03431

 

 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Martha
Ward
Sent: Tuesday, August 11, 2009 2:42 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] LYVE-1 antibody

 

Hello,

 

I wanted to know if anyone has tried this antibody on the Bond stainer,

and if so, how did it work for you?   I have purchased one from Santa

Cruz Biotechnology (cat#sc-80170) at the request of one of our

Pathologists.  Any feedback is appreciated.

 

Thanks!

 

Martha Ward

Molecular Diagnostics Lab

Wake Forest University Baptist Medical Center

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RE: [Histonet] ISH

2009-08-12 Thread Josie Britton
 

Try Novocastra and Bond Reagent products 2009.  800-248-0123 ext. 7880.

 

I hope this helps!

 

Josie Britton HT

Cheshire Medical Center

Keene, NH 03431

 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Webb,
Dorothy L
Sent: Tuesday, August 11, 2009 2:36 PM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] ISH

 

Can anyone supply me with a vendor for Kappa/Lambda ISH?  I heard that
Dako and Ventana have had to take their ASR Kappa.Lamda product off of
the market.  I am in need of where to go for ASR or IVD in this area!!

 

Thanks,

 

Dorothy Webb, HT

Regions Histology Technical Supervisor

651-254-2962

 

 

 

  

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RE: [Histonet] Blue haze

2008-12-04 Thread Josie Britton
I know this!  We have had this problem before.  We have now added and extra cap 
full ( or ½ cap full per SurgiPath) to our Define.  So instead of 2 we put 3 
in.  We also have a problem with our water filters clogging.  Make sure you 
have plenty of water pressure also, but this pretty much solved our problem.

 

Josie Britton HT

Cheshire Medical Center

580 Court Street

Keene,  NH 03431

603-354-5454 ext.2454

 

-Original Message-
From: [EMAIL PROTECTED] [mailto:[EMAIL PROTECTED] On Behalf Of Bernice Frederick
Sent: Thursday, December 04, 2008 9:06 AM
To: 'Joe Nocito'; 'Histonet Alias'; 'Marshall, Kimberly'
Cc: histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Blue haze

 

I'm sure you'll just charm them and they'll never catch on

 

 

Bernice Frederick HTL (ASCP)

Northwestern University

Pathology Core Facility

ECOGPCO-RL 

710 N Fairbanks Court

Olson 8-421

Chicago,IL 60611

312-503-3723

 

 

-Original Message-

From: [EMAIL PROTECTED]

[mailto:[EMAIL PROTECTED] On Behalf Of Joe Nocito

Sent: Wednesday, December 03, 2008 8:31 PM

To: Histonet Alias; Marshall, Kimberly

Cc: histonet@lists.utsouthwestern.edu

Subject: Re: [Histonet] Blue haze

 

I thought that was Purple Haze, by Jimi Hendrix. Oh dear me, is it Friday 

yet? Forgive me, we are in the window for CAP and I'm just all in a haze.

 

JTT

- Original Message - 

From: Histonet Alias [EMAIL PROTECTED]

To: Marshall, Kimberly [EMAIL PROTECTED]

Cc: histonet@lists.utsouthwestern.edu

Sent: Wednesday, December 03, 2008 12:08 PM

Subject: Re: [Histonet] Blue haze

 

 

 Hi Kimberly,

 Are you using a clarifier step?

 

 On Wed, Dec 3, 2008 at 12:47 PM, Marshall, Kimberly 

 [EMAIL PROTECTED] wrote:

 

 Howdy all,

 

   I have just changed over to Surgi Path's H  E system.  With the latest

 fear of running out of hematoxylin and all my Pathologist wanted us to

 change over.  Its a great stain but we have a bad haze  in the 

 background.

  It is not hurting the tissue or DX at all, but to ME it looks awful.  Is

 there anyone else out there using this?   We are not using positive 

 charged

 slides or anything added to my water bath.  Any suggestions  Thanks 

 in

 advance

 

 Kimberly Marshall HT (ASCP)

 

 

 



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RE: [Histonet] RE: Uneven HE Staining

2008-11-19 Thread Josie Britton
Sounds to me that your having a de-paraffining problem.  Check your xylene or 
clearing agent, maybe there is water in them or they are not as clean as they 
should be.  Are you on a daily rotation/change of staining/de-paraffin 
reagents?  Maybe, your oven isn't hot enough to melt some paraffin off the 
slides before de-par!

 

Josie Britton HT  

 

-Original Message-
From: [EMAIL PROTECTED] [mailto:[EMAIL PROTECTED] On Behalf Of Gudrun Lang
Sent: Wednesday, November 19, 2008 9:48 AM
To: histonet@lists.utsouthwestern.edu
Subject: AW: [Histonet] RE: Uneven HE Staining

 

Are the coplin jars all equally filled? If the wash-jars are partly filled,

the lower slides would be more differentiated than the upper.

Gudrun

 

-Ursprüngliche Nachricht-

Von: [EMAIL PROTECTED]

[mailto:[EMAIL PROTECTED] Im Auftrag von Karla

Arrington

Gesendet: Mittwoch, 19. November 2008 02:34

An: histonet@lists.utsouthwestern.edu

Betreff: [Histonet] RE: Uneven HE Staining

 

Recently we have had an issue with uneven HE staining.  Lately slides that

have 

three sections on one slide, mostly GI biopsies, and the last section

(bottom of 

slide) are paler than the upper two section.  All cut by the same person and

the 

stains were great.  What could be the cause of this?  Also with the quality

of 

formalin.  Can formalin be purchased as bad when it takes 6 days to fix

placenta 

or breasts?  What is the cause? 

 

Karla Arrington, HT(ASCP)

 

 

  

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RE: [Histonet] Dako

2008-11-18 Thread Josie Britton
Hi,

 

We just got the new Bond Max IHC stainer and we love it.  You just cut
the slides dry them and place them on the Bond.  It does retrieval,
antibody staining, and counter stain.  You just dehydrate , clear, and
mount your coverslip.  It is easy to use.  It has 3 individual slide
tray's of 10.  You can load more slides on the empty tray's and start a
new batch while the others are running.  We run into the pathologist's
adding more antibodies to the list an hour after we have run the first
batch frequently, so this feature is great.  When you add more IHC's the
run time on all the slide tray's run times do increase, but it's better
than having to wait another 2-3 hours to put your next set of immuno's
on.

 

Hope this helps!

 

Josie Britton HT

Cheshire Medical Center

580 Court Street

Keene, NH 03431


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