Re: [Histonet] inverted meniscus

2010-08-11 Thread Jackie M O'Connor
Maybe it twisted it's knee while out playing touch football.



From:
Mary Benoit mbp...@yahoo.com
To:
histonet@lists.utsouthwestern.edu
Date:
08/11/2010 01:21 PM
Subject:
[Histonet] inverted meniscus
Sent by:
histonet-boun...@lists.utsouthwestern.edu



Today while perfroming an xylene purity check after recyling xylene on a 
CBG recycler, I noticed that the meniscus  between the DH2O and Xylene is 
inverted...that is convex instead of concave.  I have done this check many 
times( you add exactly 15 mls of water to exactly 85 mls xylene, invert 
and allow to settle out and observe the meniscus at the separation 
site for changes in volume of water) and have never seen it invert.  The 
glass cyclinder was clean , we repeated three times and still same 
results.  Anyone have a clue as to why?  CBG did not have an answer .  
thanks
Mary F Benoit MT(ASCP)
The Pathology Laboratory
Lake Charles, LA


 
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Re: [Histonet] Sakura Tape coverslipper

2010-08-11 Thread Jackie M O'Connor
OMG.   This problem was ever present in our lab for years, until I figured 
out that ANY minute trace of moisture, water, eosin in the last absolute 
alcohol would interfere with the activation of the adhesive in the tape, 
and create this brown artefact.   We religiously change our absolute 
alcohols on the autostainer so the last alcohol is perfectly clear of any 
hint of eosin, and the artefact has disappeared from our tape-coverslipped 
slides.The Sakura rep couldn't help me either, and told me they had 
NEVER seen this problem before.   Love it.

Keep your last 100% PRISTINE, and the artefact will be eliminated.   I 
promise.

Jackie O'






From:
Nails, Felton flna...@texaschildrens.org
To:
'Gauch, Vicki' gau...@mail.amc.edu, 
histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
Date:
08/11/2010 01:45 PM
Subject:
[Histonet] Sakura Tape coverslipper
Sent by:
histonet-boun...@lists.utsouthwestern.edu



 
Has anyone been experiencing a brown cornflaking artifact on their slides 
after being coverslipped.
I was told by Sakura that it was do to the slides drying out when 
transferred from the stainer to the coverslipper.
Which can't be correct because on the new sakura coverslipper there is a 
holding area which is filled with xylene so if the tissue dried out it 
would rehydrate before being coverslipped. 

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Re: [Histonet] Reagent Grade Alcohol Brands

2010-08-09 Thread Jackie M O'Connor
What kind of issues?   I'm considering switching over to all Surgipath 
(Leica) products.  I'd like to hear more of this. 




From:
kristen arvidson arvidsonkris...@yahoo.com
To:
histonet histonet@lists.utsouthwestern.edu
Date:
08/09/2010 12:05 PM
Subject:
[Histonet] Reagent Grade Alcohol Brands
Sent by:
histonet-boun...@lists.utsouthwestern.edu



Hello All,
What brands of reagent grade ETOH is everyone using??  Leica is having 
some manufacturing issues...need some ASAP!!


 
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[Histonet] Elgin Community College Histology Program

2010-07-13 Thread Jackie M O'Connor
Does anyone know who is running this program?   I would like to contact 
them.
Thanks!
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Re: [Histonet] (no subject)

2010-07-07 Thread Jackie M O'Connor
Ask management if he would suddenly be a better technician and more 
valuable if he passed the exam?   Duh - no.   In my opinion, merit 
increases should be based on merit - not documentation. 
If he's not eligible, he's not eligible.  Does your management increase 
pay based on certification?   So, if a certified tech with one year of 
experience came to your lab, they would be paid more than an incumbent 
tech with 8 years experience?  Sounds like you have some dinosaur 
management there. 



From:
Fredrickson, Mona mfredrick...@nrh-ok.com
To:
Histonet@lists.utsouthwestern.edu Histonet@lists.utsouthwestern.edu
Date:
07/07/2010 12:04 PM
Subject:
[Histonet] (no subject)
Sent by:
histonet-boun...@lists.utsouthwestern.edu



Hello All in Histoland,
I have a tech who is employed as Histotech eligible, but he was not able 
to pass the HT exam and now is no longer eligible to thake the test 
because he has to get his associates degree in science.  The lab 
management wants to change his title from histotech eligible to histotech 
non-registered without pay increase.  But I feel the pay should be 
increased. So I would appreciate comments on the following:
1.) should title be changed from eligible to non-registered?
2.) After having done this for 8 years should his pay stay the same?
3. Should job responsibilities remain the same
 Thank you in advance for feedback!
Histotech in Oklahoma

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RE: [Histonet] (no subject)

2010-07-07 Thread Jackie M O'Connor
Over the years, I have had some HT and HTL registered technologists who 
were crummy technicians.   I'm jus' sayin' that certification doesn't 
automatically mean you are better than a non-certified tech. 




From:
Gunderson, Michael mgund...@fairview.org
To:
Jackie M O'Connor Jackie.O'con...@abbott.com, Fredrickson, Mona 
mfredrick...@nrh-ok.com
Cc:
Histonet@lists.utsouthwestern.edu Histonet@lists.utsouthwestern.edu, 
histonet-boun...@lists.utsouthwestern.edu 
histonet-boun...@lists.utsouthwestern.edu
Date:
07/07/2010 12:31 PM
Subject:
RE: [Histonet] (no subject)



By telling someone they should earn the same without passing our 
registration exam diminishes the effort and hard work of registered HT and 
HTL's.  Management are not dinosaurs, they are fair.   The exam is there 
to weed out the weak and under or un-qualified, if you cannot pass the 
test, you have not earned the right of those who have.

Michael A. Gunderson HTL(ASCP)
Lead Technologist-Immunostains Laboratory
University of Minnesota Medical Center-Fairview
2450 Riverside Avenue
Minneapolis, MN 55454


Laboratory: 1-612-273-9119
Fax: 1-612-273-4879
Email: mgund...@fairview.org

From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jackie M O'Connor 
[Jackie.O'con...@abbott.com]
Sent: Wednesday, July 07, 2010 12:09 PM
To: Fredrickson, Mona
Cc: Histonet@lists.utsouthwestern.edu; 
histonet-boun...@lists.utsouthwestern.edu
Subject: Re: [Histonet] (no subject)

Ask management if he would suddenly be a better technician and more
valuable if he passed the exam?   Duh - no.   In my opinion, merit
increases should be based on merit - not documentation.
If he's not eligible, he's not eligible.  Does your management increase
pay based on certification?   So, if a certified tech with one year of
experience came to your lab, they would be paid more than an incumbent
tech with 8 years experience?  Sounds like you have some dinosaur
management there.



From:
Fredrickson, Mona mfredrick...@nrh-ok.com
To:
Histonet@lists.utsouthwestern.edu Histonet@lists.utsouthwestern.edu
Date:
07/07/2010 12:04 PM
Subject:
[Histonet] (no subject)
Sent by:
histonet-boun...@lists.utsouthwestern.edu



Hello All in Histoland,
I have a tech who is employed as Histotech eligible, but he was not able
to pass the HT exam and now is no longer eligible to thake the test
because he has to get his associates degree in science.  The lab
management wants to change his title from histotech eligible to histotech
non-registered without pay increase.  But I feel the pay should be
increased. So I would appreciate comments on the following:
1.) should title be changed from eligible to non-registered?
2.) After having done this for 8 years should his pay stay the same?
3. Should job responsibilities remain the same
 Thank you in advance for feedback!
Histotech in Oklahoma

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of the designated recipients named above. If you are not
the intended recipient, you are hereby notified that you
have received this communication in error and that any
review, disclosure, dissemination, distribution, or copying
of it or its contents is prohibited. If you have received
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Re: [Histonet] ARTICLE

2010-06-25 Thread Jackie M O'Connor
No - but I could write one.




From:
Sara Baldwin/mhhcc.org sbald...@mhhcc.org
To:
histonet@lists.utsouthwestern.edu
Date:
06/25/2010 10:53 AM
Subject:
[Histonet] ARTICLE
Sent by:
histonet-boun...@lists.utsouthwestern.edu



Hi Histonetters
My boss was wondering if anyone has come across an article a long time ago 
(about 10 years) that was called Workplace Violence in the Laboratory

Thanks
Pathology Supervisor
Kathy Baldwin, SCT (ASCP)
Memorial Hospital and Health Care Center
sbald...@mhhcc.org
Ph 812-482-0210, 482-0216,  Fax 812-482-0232, 
Pager 812-481-0897
Confidential information, Authorized use only.

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

2010-06-22 Thread Jackie M O'Connor
A good ol' hot appendix works great.   Not as good as a Slim Jim, tho.
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Re: [Histonet] afb contamination

2010-05-21 Thread Jackie M O'Connor
You can eliminate the crossover contamination by performing the stain 
horizontally on a staining rack.  A lot of labs re-use the carbol fuchsin, 
which can have lots of extraneous AFB floating around, waiting patiently 
to attach itself to an unsuspecting patient slide.  Using the staining 
rack, you don't use a lot of reagent, and you never cross-contaminate.




From:
Tench, Bill bill.te...@pph.org
To:
histonet@lists.utsouthwestern.edu
Date:
05/21/2010 02:34 PM
Subject:
[Histonet] afb contamination
Sent by:
histonet-boun...@lists.utsouthwestern.edu



We had a problem with contamination on our AFB stains, and we discovered
that it was the control slide flaking off in the copland jar which was
being used for staining the control and target slide at the same time
(makes sense as a real control').  We identified these contaminants
because they were frequently large clusters (by large I would say 4-8
organisms) which we almost never see in real cases, and fortunately,
they were also not in the same plane of focus (but that can be subtle).
they did create problems.  Our solution was to stain the control
separately from the case.  No more problems. 

 

Bill Tench

Associate Dir. Laboratory Services

Chief, Cytology Services

Palomar Medical Center

555 E. Valley Parkway

Escondido, California  92025

bill.te...@pph.org

Voice: 760- 739-3037

Fax: 760-739-2604

 


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RE: [Histonet] alternative for bunsen burner?

2010-05-18 Thread Jackie M O'Connor
I think that's the crux of her question - what can she use as an 
alternative?   You can find forceps warmers here.   
http://americanmastertech.com/store/main.aspx?p=ItemDetailStylesitem=EQFW-120
Although, I still miss the ol' bunsen burner.   It was great for burning 
away little fragments of tissue from between the teeth - of the forceps, 
not my teeth. 



From:
Mike Pence mpe...@grhs.net
To:
Brandi Higgins brandihigg...@gmail.com, 
histonet@lists.utsouthwestern.edu
Date:
05/18/2010 11:42 AM
Subject:
RE: [Histonet] alternative for bunsen burner?
Sent by:
histonet-boun...@lists.utsouthwestern.edu



Why are you still using a bunsen burner? I believe there is a CAP
question about No open flames in the lab. I would suggest finding a
replacement.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Brandi
Higgins
Sent: Tuesday, May 18, 2010 10:30 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] alternative for bunsen burner?


Hello all,

Our hospital is moving our histology department across the hall and have
asked us if we can find an alternative to the bunsen burner so they
don't have to install a gas line.  The pathologist has told me that
there is some machine that can be used instead of a flame to burn the
forceps while embedding (which is our main use for the bunsen flame).
This is the only lab I have ever worked at and I don't know what such a
machine would be called.  If anyone knows the name, or any other
alternative method can you let me know.  Model numbers/companies would
be a bonus too!  Thanks so much for your help.

Brandi Higgins, BS, HT(ASCP)
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[Histonet] FREE MONEY!

2010-03-30 Thread Jackie M O'Connor
Now that I have your attention - - 

I would really like to hear from you if you are at all interested in a 
histology position at Abbott Laboratories in Northern Illinois.   Even if 
you have applied previously. 

This is a great opportunity to work in a GLP research lab, a good deal of 
bench work, but developing IHC for toxicology purposes as well.   We have 
a Biocare intelliPATH stainer - it's FUN!

We have four full time technicians/technologists with a fifth open 
position.   Abbott offers 3 weeks paid vacation, great benefits, and is a 
good company to work for.   I've been here ten years, and I've never been 
anywhere 10 years.

Please forward your resume to me, as well as go to www.Abbott.com to 
apply. 

Jackie O'Connor
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[Histonet] Job Opportunity

2010-03-25 Thread Jackie M O'Connor
We have a great full time permanent opportunity for an experienced 
histotech at Abbott Laboratories in Abbott Park, IL. We are about 40 miles 
north of Chicago in Lake County.   Please go to www.Abbott.com if you are 
interested in applying for this position.   Additionally, if you would 
like to forward your resume to me, it could be helpful. 

Jackie O'
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Re: [Histonet] lab spill clean-up

2009-11-05 Thread Jackie M O'Connor
I've always been in institutions (hey, no jokes) where more than a liter 
of spilled formalin, alcohol, xylene, etc is cleaned up by the in house 
haz mat people.



From:
kristen arvidson arvidsonkris...@yahoo.com
To:
histonet histonet@lists.utsouthwestern.edu
Date:
11/05/2009 02:22 PM
Subject:
[Histonet] lab spill clean-up
Sent by:
histonet-boun...@lists.utsouthwestern.edu



I am looking for quantities of various lab chemicals that are considered 
safe for lab personnel to clean up.  Are there set guidelines for when you 
should call for help?


 
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[Histonet] Looking for Ray Ortiz

2009-11-05 Thread Jackie M O'Connor
Can someone tell Ray to contact me?  Thanks.
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Re: [Histonet] Arm Rests

2009-11-03 Thread Jackie M O'Connor
Yeah - don't use em.  Since I had developed tendinitis in both elbows from 
microtomy,  EHS ergonomics people at a former employer decided to invent 
some.  They covered them with some fake vinyl material, and the very first 
day I tried using them, my elbow slipped on the shiny vinyl and I cut off 
the tip of my finger on the blade.   I have since learned that resting 
your forearms on the sharp edge of the bench caused my tendinitis.   Since 
I quit that bad habit, I haven't had a recurrence in 15 years -  nor have 
I cut myself.



From:
Weems, Joyce jwe...@sjha.org
To:
histonet@lists.utsouthwestern.edu
Date:
11/03/2009 12:58 PM
Subject:
[Histonet] Arm Rests
Sent by:
histonet-boun...@lists.utsouthwestern.edu



Does anyone have a recommendation for microtome arm rests? Thanks in
advance! 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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[Histonet] Canine endothelial antibody

2009-10-28 Thread Jackie M O'Connor
A week or so ago I thought I saw a post about an antibody that works for 
canine endothelial cells, but I can't find it in the archives - was I just 
dreaming, because I need this so bad?   I've tried Factor VIII and a CD34 
on FFPE, but with poor results.   Any help would be most appreciated.
Thanks,
Jackie O'

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Re: [Histonet] Floaters in Waterbath

2009-10-23 Thread Jackie M O'Connor
Kim wipes seem to pick up more debris than paper towels, and they pick up 
much less water.   We routinely sweep the waterbath with a kimwipe after 
each block.   You can also pick up floaters from embedding if the forceps 
are not cleaned between each block.   Most embedding centers have multiple 
wells for forceps - how often do you clean those wells?  You'd be amazed 
at how much gunk accumulates in there! 



From:
Stella Mireles estellamire...@gmail.com
To:
Histonet@lists.utsouthwestern.edu
Date:
10/23/2009 09:11 AM
Subject:
[Histonet] Floaters in Waterbath
Sent by:
histonet-boun...@lists.utsouthwestern.edu



I know we have all had some problems with floaters in our waterbath at 
some
point in our microtomy career.
Our doctors are very picky and I need some tips on keeping an immaculate
clean waterbath, but not sacrificing the speed in a regular
routine lab.  We use the pyrex waterbath and paper towels for wiping our
area.

Thanks
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RE: [Histonet] human macrophages in human melanoma xenografts

2009-10-23 Thread Jackie M O'Connor
Naira - 
These are presumably SCID mice?  You can use a mouse mAb with no Ig 
interference, since SCIDs do not have an immune system.  You can get the 
rare 'leaker', but I've used murine mAb routinely for human xenografts in 
SCIDs.  Now, Nudes are a different story.




From:
Margaryan, Naira nmargar...@childrensmemorial.org
To:
Liz Chlipala l...@premierlab.com, Galbraith, Joe 
joseph-galbra...@uiowa.edu, histonet@lists.utsouthwestern.edu 
histonet@lists.utsouthwestern.edu
Date:
10/23/2009 10:59 AM
Subject:
RE: [Histonet] human macrophages in human melanoma xenografts
Sent by:
histonet-boun...@lists.utsouthwestern.edu



Thanks a lot both of you!

For melanoma detection, I usually use HRP with AEC. Is there any non-mouse 
anti-human macrophage marker?

Thank you much,
Naira 


-Original Message-
From: Liz Chlipala [mailto:l...@premierlab.com] 
Sent: Friday, October 23, 2009 10:51 AM
To: Galbraith, Joe; Margaryan, Naira; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] human macrophages in human melanoma xenografts 

F4/80 is a mouse macrophage marker.  If she wants to detect human
macrophages in a mouse background she will need to use a mouse
anti-human CD68.  She will need to run it with a mouse on mouse
detection system and run all of the appropriate negative controls.  I
would also select a alkaline phosphatase detection system rather than
HRP with DAB just incase the tumor has any melanin in it.  I have done
this before looking for human lymphocytes with LCA in a mouse
background.  You just need to make sure you have all of the appropriate
controls.  For a positive control I would use a human tonsil or
something like that and you need to make sure you run the appropriate
isotype negative controls. 

Liz

Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
Manager
Premier Laboratory, LLC
PO Box 18592
Boulder, Colorado 80308
office (303) 682-3949 
fax (303) 682-9060
www.premierlab.com
 
 
Ship to Address:
1567 Skyway Drive, Unit E
Longmont, Colorado 80504

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Galbraith, Joe
Sent: Friday, October 23, 2009 9:44 AM
To: Margaryan, Naira; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] human macrophages in human melanoma xenografts 

Naira:

Here is a link to a site listing macrophage markers.  F4/80 is a
commonly mentioned marker for macrophages.  I presume you mean IHC
rather than ICH.  Enjoy.

http://www.antibodybeyond.com/reviews/cell-markers/macrophage-marker.htm

Joe
joseph-galbra...@uiowa.edu


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Margaryan, Naira
Sent: Friday, October 23, 2009 10:31 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] human macrophages in human melanoma xenografts 

Hi Histonetters,

I would like to be able to look at human macrophages in human melanoma
xenografts raised in mouse. Could you please suggest me a best Ab for
ICH and protocol?



Thanks in advance,

Naira


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RE: [Histonet] RE: Asbestos Body Digestion

2009-09-22 Thread Jackie M O'Connor
When I was in Honolulu, loaded with shipyards - we frequently digested 
lung tissue in sodium hypochlorite (bleach) to get an aggregate of 
asbestos fibers (if they were present). I don't recall the exact 
procedure, but it was quite common then.  We were requested to do this by 
lawyers, mostly.  So, I'm really not much help, just full of useless 
rhetoric.   Hugh Luk might remember doing this?



From:
Weems, Joyce jwe...@sjha.org
To:
histonet@lists.utsouthwestern.edu
Date:
09/22/2009 01:29 PM
Subject:
RE: [Histonet] RE: Asbestos Body Digestion
Sent by:
histonet-boun...@lists.utsouthwestern.edu



Just trying to help a patient. I have a patient who wants to know if her
lung adenoca could be tested to see if any asbestos could be involved.
One of my pathologists suggested I call Mayo. Nothing there. He said
someone used to do the digestion procedure at SUNY. So I asked the
experts. I have a procedure from Lynette but I think I need an expert to
do the testing and the resulting. 
Joyce

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rittman,
Barry R
Sent: Tuesday, September 22, 2009 14:15
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: Asbestos Body Digestion

Joyce
Why do you want to dissolve these?
I seem to remember that these are usually characteristic shaped
structures that are iron positive and should be easy to identify on
morphology alone or am I mistaken?
Barry

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Weems,
Joyce
Sent: Tuesday, September 22, 2009 10:47 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Asbestos Body Digestion

Does anyone know about a digestion procedure for asbestos bodies on FFPE
lung tissue? Our pathologist remembers that someone used to do this at
SUNY. I'd appreciate your feedback. 
 
Thanks,
Joyce
 

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] mice legs

2009-09-15 Thread Jackie M O'Connor
I did a lot of  IHC work with whole mouse legs where we had to pay close 
attention to the tibia, as well as the joint.When the mice were 
necropsied, I had the prosectors remove all the soft tissue and foot 
without disrupting the joint.  They could do this easily with fresh tissue 
as opposed to after fixation.   The leg bones were fixed for no more than 
48 hours, and decalcified in home-brewed 5% formic acid overnight on a 
shaker table.   I then trimmed them to expose the joint and bone marrow 
prior to processing on a routine program, about 45 minutes per station. 
Perfect ever single time.  IHC was beautiful. 

Hope this helps.

Jackie O'




From:
Shaw, Sharon shs...@wpi.edu
To:
histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
Date:
09/15/2009 08:46 AM
Subject:
[Histonet] mice legs
Sent by:
histonet-boun...@lists.utsouthwestern.edu



Good Morning Histo World,

I would like to know if anyone is working with mice legs, I have a PI that 
I work with that wants to process the whole leg, the problem is I need to 
decal it first and is wondering if the decal will break down the tissue, I 
think it would he doesn't think so. And if anyone has do this would it be 
possible to share your protocol with me from decal to processing.

Thanks,
Sharon- WPI
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Re: [Histonet] formalin storage

2009-09-11 Thread Jackie M O'Connor
I once had my safety officer insist I wear chain maille gloves while 
cutting frozen sections.  They didn' t care about all the reasons I gave 
them why I shouldn't - like it would be impossible to use the machine 
while wearing them, and the patient would have to lie on the operating 
table longer waiting to find out if their entire colon was going to be 
removed. 



Jean Warren jwarre...@cinci.rr.com 
Sent by: histonet-boun...@lists.utsouthwestern.edu
09/11/2009 08:25 AM

To
Riesen, Rebecca rebecca.rie...@nchmd.org, 
histonet@lists.utsouthwestern.edu
cc

Subject
Re: [Histonet] formalin storage






No, it is ridiculous. Safety people tried to argue this with us years ago. 

One of our pathologists told them, How can something that is almost 90% 
water be a combustion hazard?


- Original Message - 
From: Riesen, Rebecca rebecca.rie...@nchmd.org
To: histonet@lists.utsouthwestern.edu
Sent: Friday, September 11, 2009 9:15 AM
Subject: [Histonet] formalin storage




We have been directed by our Safety Officer to store all formalin (37%
and 10% NBF) in a flammable storage room, cabinet or container.  Yes,
37% Formalin we do store in this manner, but I have never heard of this
requirement for 10%NBF.  I looked on line to many MSDS sheets from
different vendors and found only one that stated such storage
requirements for 10% NBF.  During this search I found all but one
company states that formalin is not flammable.  I brought this to the
Safety Officer.  He agrees that it is not flammable but that it IS
combustible.  Combustible=Flash point of 100F to 200F.  Of the dozen
sites I visited I found the following data concerning the Flash Point of
10% NBF: from NA / 200F / 122F to 185F.  The NFPA (National Fire
Protection Agency) guideline of no more than 1 gallon in a flammable
storage container and 1 gallon outside of a safety cabinet/container per
100 square feet is already quite limiting.  Using this guideline, we
have calculated acceptable volumes of the known flammables (Alcohols and
Xylenes) we can store.  Adding 10% NBF to the equation will have us
traveling to our bulk storage area constantly.  Does anyone out there
store 10%NBF in flammable cans/cabinets?
Riesen, Rebecca
rebecca.rie...@nchmd.org
NCH Healthcare Systems
Direct 239-436-5000 x2188
Fax 239-436-6767


Visit our website at http://www.nchmd.org


CONFIDENTIALITY NOTICE

This email and any files transmitted with it are from the NCH Healthcare 
System.
This message is confidential and is intended only for the addressee. If 
you 
are
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call 
us
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promptly
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Re: [Histonet] formalin storage

2009-09-11 Thread Jackie M O'Connor
To prevent getting cut on the knife. 



Emily Sours talulahg...@gmail.com 
09/11/2009 08:34 AM

To
Jackie M O'Connor Jackie.O'con...@abbott.com, 
histonet@lists.utsouthwestern.edu
cc

Subject
Re: [Histonet] formalin storage






I have to ask--what was the point of chain mail gloves?!

Emily

One of the defining characteristics of modern surgery was that patients 
ought to survive it.
--Peter Stanley, For Fear of Pain: British Surgery, 1790-1850


On Fri, Sep 11, 2009 at 9:31 AM, Jackie M O'Connor 
Jackie.O'con...@abbott.com wrote:
I once had my safety officer insist I wear chain maille gloves while
cutting frozen sections.  They didn' t care about all the reasons I gave
them why I shouldn't - like it would be impossible to use the machine
while wearing them, and the patient would have to lie on the operating
table longer waiting to find out if their entire colon was going to be
removed.



Jean Warren jwarre...@cinci.rr.com
Sent by: histonet-boun...@lists.utsouthwestern.edu
09/11/2009 08:25 AM

To
Riesen, Rebecca rebecca.rie...@nchmd.org,
histonet@lists.utsouthwestern.edu
cc

Subject
Re: [Histonet] formalin storage






No, it is ridiculous. Safety people tried to argue this with us years ago.

One of our pathologists told them, How can something that is almost 90%
water be a combustion hazard?


- Original Message -
From: Riesen, Rebecca rebecca.rie...@nchmd.org
To: histonet@lists.utsouthwestern.edu
Sent: Friday, September 11, 2009 9:15 AM
Subject: [Histonet] formalin storage




We have been directed by our Safety Officer to store all formalin (37%
and 10% NBF) in a flammable storage room, cabinet or container.  Yes,
37% Formalin we do store in this manner, but I have never heard of this
requirement for 10%NBF.  I looked on line to many MSDS sheets from
different vendors and found only one that stated such storage
requirements for 10% NBF.  During this search I found all but one
company states that formalin is not flammable.  I brought this to the
Safety Officer.  He agrees that it is not flammable but that it IS
combustible.  Combustible=Flash point of 100F to 200F.  Of the dozen
sites I visited I found the following data concerning the Flash Point of
10% NBF: from NA / 200F / 122F to 185F.  The NFPA (National Fire
Protection Agency) guideline of no more than 1 gallon in a flammable
storage container and 1 gallon outside of a safety cabinet/container per
100 square feet is already quite limiting.  Using this guideline, we
have calculated acceptable volumes of the known flammables (Alcohols and
Xylenes) we can store.  Adding 10% NBF to the equation will have us
traveling to our bulk storage area constantly.  Does anyone out there
store 10%NBF in flammable cans/cabinets?
Riesen, Rebecca
rebecca.rie...@nchmd.org
NCH Healthcare Systems
Direct 239-436-5000 x2188
Fax 239-436-6767


Visit our website at http://www.nchmd.org


CONFIDENTIALITY NOTICE

This email and any files transmitted with it are from the NCH Healthcare
System.
This message is confidential and is intended only for the addressee. If
you
are
not the intended recipient or have received this email in error, please
call
us
immediately at (239) 436-5000 and ask to speak to the message sender or
promptly
email the message sender of the delivery error and then delete the
message.
Thank you.


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Re: [Histonet] Decal Solution

2009-09-03 Thread Jackie M O'Connor
I have decalled whole mouse legs (soft tissue removed).  Use 5% formic 
acid for 24 hours on a shaker table.





Shaw, Sharon shs...@wpi.edu 
Sent by: histonet-boun...@lists.utsouthwestern.edu
09/03/2009 01:09 PM

To
histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
cc

Subject
[Histonet] Decal Solution






Hi Histo world,

I have a crazy question, I work in research facility and one of the 
investigators needs decal done on mice legs, they never check to see if we 
had decal solution before they began the procedure, of course we don't. I 
tried different companies to order some but they can't overnight the 
solution because it is a hazard. Does anyone have a protocol
that they use in making  a decal solution? The old histology books do but 
I was looking for maybe an updated solution.
Please send my your suggestions they want this done ASAP.

Thanks,
Sharon Shaw
WPI
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Re: [Histonet] Best IHC stainer

2009-08-27 Thread Jackie M O'Connor
Agreed.   Intellipath from Biocare.   Load it and walk away - and it has a 
voice notification to tell you the run is finished.   You can load it in 
the PM, and take slides off in the AM.  Love it.   Has a chilling station 
for AP chromogen, too.

Jacke O'



godsgal...@aol.com 
Sent by: histonet-boun...@lists.utsouthwestern.edu
08/27/2009 10:05 AM

To
gareth.da...@hotmail.com, histonet@lists.utsouthwestern.edu
cc

Subject
Re: [Histonet] Best IHC stainer







Ventana reagents eem to be a little pricey, but if you want a system that 
you can load and walk away from, it is the way to go.  DAKO is an easy 
enough to use instrument and is an open system, but they are going to a 
price per slide kind of thing, if I remmeber correctly.



I prefer the IP from Biocare, as is is an open system and a continuous 
load instrument.  And it mixes the chromagen online


-Original Message-
From: Gareth Blaeuer Davis gareth.da...@hotmail.com
To: histonet@lists.utsouthwestern.edu
Sent: Wed, Aug 26, 2009 8:04 pm
Subject: [Histonet] Best IHC stainer





he lab I work in has been doing demos on IHC stainers Ventana Benchmark XT 
and 
ako's Autostainer Plus.  We could really use feed back
from current users of both.  We are having a hard time deciding between 
the two, 
o any input would be great.
What are the Pros and Cons with both.
Thanks,
Gareth Blaeuer Davis, B.S., HT
 
_
otmail® is up to 70% faster. Now good news travels really fast. 
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Re: [Histonet] CD31 working protocol

2009-08-10 Thread Jackie M O'Connor
Biocare has a CD31 anti mouse that does stain FFPE.I personally think 
nothing will ever compare with the Santa Cruz goat that no longer is 
available - but Biocare does work.





Zerfas, Patricia (NIH/OD/ORS) [E] zerf...@ors.od.nih.gov 
Sent by: histonet-boun...@lists.utsouthwestern.edu
08/10/2009 01:50 PM

To
'histonet@lists.utsouthwestern.edu' histonet@lists.utsouthwestern.edu
cc

Subject
[Histonet] CD31 working protocol






Dear Listservers,
I have tried MANY protocols and I am unable to obtain a 
working protocol for the CD31 antibody.
I have tried both the CD31 rat monoclonal and a CD31 rabbit 
polyclonal.

Thanks in advance for your help.

Patricia Zerfas
National Institutes of Health
Building 28A, Room 112
28 Library Drive
Bethesda, MD  20892
ph:   (301) 496-4464
fax:  (301) 402-1068

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Re: [Histonet] reagents for IHC

2009-08-03 Thread Jackie M O'Connor
Biocare.  Biocare.  Biocare.



Margaryan, Naira nmargar...@childrensmemorial.org 
Sent by: histonet-boun...@lists.utsouthwestern.edu
08/03/2009 03:19 PM

To
histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
cc

Subject
[Histonet] reagents for IHC






Hi everyone,

How are you experiencing the economic pressures and price changes for 
REAGENTS? I am sorry, but I just bought reagents from DAKO and, for the 
price I paid for 125 ml before, I got 15-50 ml :(

I am ready to switch to another company, but I need your suggestion about 
reagents for IHC and companies you are purchasing from: Peroxidase Block, 
Protein Block, Antibody diluents, DAB, AEC, different secondaries and 
tertiaries.

Thanks in advance,
Naira

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Re: [Histonet] Biocare IntelliPATH Flex Immunostainer

2009-07-28 Thread Jackie M O'Connor
We have had it since February-ish.   Love it.   No problems.   Great 
customer service.   It talks to you, too - like my GPS.

Jackie O'



Jessica Piche jessgro...@yahoo.com 
Sent by: histonet-boun...@lists.utsouthwestern.edu
07/28/2009 01:44 PM

To
histonet histonet@lists.utsouthwestern.edu
cc

Subject
[Histonet] Biocare IntelliPATH Flex Immunostainer






 
Hi All,
We are just wondering if anyone out there is using the Biocare IntelliPATH 
Flex Immunostainer? If so how do you like it? Any problems? How long have 
you had it? And any other information you could provide about it would be 
great.
Thanks,

Jessica Piche-Grocki, HT(ASCP)
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Re: [Histonet] Modified Davidson's fixative use

2009-06-08 Thread Jackie M O'Connor
To not answer your question - we fix eyes and testes in Modified Davidsons 
for 48 hours then transfer to formalin to await processing. 
Since mDF is basically formalin, alcohol, and gaa - a water rinse step is 
pretty moot.






Johnson, Teri t...@stowers.org 
Sent by: histonet-boun...@lists.utsouthwestern.edu
06/08/2009 10:56 AM

To
histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
cc

Subject
[Histonet] Modified Davidson's fixative use






Dear colleagues,

For those who use modified Davidson's fixative for your samples, do you do 
a water rinse prior to starting them in alcohol dehydration series, or 
simply go from fixative into the alcohol?

Thanks!

Teri Johnson, HT(ASCP)QIHC
Managing Director Histology Facility
Stowers Institute for Medical Research
1000 E. 50th St.
Kansas City, MO 64110


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Re: [Histonet] nice one Kemlo

2009-04-05 Thread Jackie M O'Connor
My grandfather from Slovakia was Jan.  My name is Jackie, I have five 
sisters, two are Jeri and Stevie.   My parents had a son after they had 
five daughters and named him Ernie.Sometimes people just run out of 
good names for their kids.I happen to like Rene'.   It beats Apple or 
Moon Unit Zappa.
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RE: [Histonet] Leica Bond Max - any opinions?

2009-04-01 Thread Jackie M O'Connor
I agree with Linda.   I researched 5 different automated IHC stainers to 
be used for toxicology research applications, and found the intelliPATH to 
be the best solution for our needs.
Biocare, as well, has a vast array of anti rat and mouse primary 
antibodies and detection systems.   Additionally, the cost for the 
intelliPATH is quite reasonable, compared to the other platforms.

Jackie O'




Blazek, Linda lbla...@digestivespecialists.com 
Sent by: histonet-boun...@lists.utsouthwestern.edu
04/01/2009 06:22 AM

To
'Michelle MacVeigh-Aloni' macve...@usc.edu, 
histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
cc

Subject
RE: [Histonet] Leica Bond Max - any opinions?






I would really suggest you look closely at the Intellipath from BioCare. 
They are a truly open system.
Linda

Linda Blazek HT (ASCP)
Manager/Supervisor
GI Pathology of Dayton
7415 Brandt Pike
Huber Heights, OH 45424
Phone: (937) 293-4424 ext 7118
Email: lbla...@digestivespecialists.com

 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Michelle 
MacVeigh-Aloni
Sent: Tuesday, March 31, 2009 8:39 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Leica Bond Max - any opinions?

Hi all,

I am researching the Leica Bond Max immunostainer and I like its features 
as advertised. 

The advertisement however states that the system is completely open, but 
after discussing it in length with the Leica rep I am finding that this is 
actually not so... 

We are a research core and work with mice and rats. Most of the pre-made 
antibody are designed towards human tests, so we won't use them. Then we 
would still be stuck with lots of money for consumables (as I understood 
all sold as kits with the antibodies included). We won't be using any of 
the antibodies, only the rest of the solutions... Is there a way out of 
this trap? Is there something that I didn't understand?

My question is: 
Does anybody use Leica Bond as an open system and use other companies 
antibody, buffers and antigen retrieval protocols? If you do, what have 
you done so far? (Would you share your protocols?) We like the BioCare 
products and our helpful rep :-) 
Did anybody purchase the Research dongle? Do we really need it? How did it 
help you improve your applications? I was told that depending on what I 
want unlocked, we would have to spend $14000 to $27000 extra for it. 
OUCH!!! This is not a hospital where we can charge the insurance or 
patients for this... 

I need this info ASAP, because we have to make our decision in a day and 
there is no time to demo the unit (nor anything else).
I understand that it is great for pathology, but how about animal 
research? It costs A LOT!!! We better know what are we getting ourselves 
into.

 Please help! Any advise and suggestions that I can get would be highly 
appreciated.

Michelle Mac Veigh Aloni MS, HTL
USC School of Medicine 
Department of GI and Liver
Los Angeles, CA
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Re: [Histonet] Intellipath Instrument

2009-03-20 Thread Jackie M O'Connor
We have also recently purchased this instrument.  I highly recommend it.





Sheila Haas micropathl...@yahoo.com 
Sent by: histonet-boun...@lists.utsouthwestern.edu
03/20/2009 09:28 AM

To
histonet@lists.utsouthwestern.edu
cc

Subject
[Histonet] Intellipath Instrument






A colleague of mine is looking into purchasing an immuno stainer. Biocare
has offered a good price on the Intellipath instrument, antibodies and 
reagents. While we know the antibodies are reagents are excellent, we 
know nothing about their instrumentation. Does anyone have any first 
hand experience with the Intellipath instrument, service from Biocare, 
etc...? Any information would be helpful.
Thank you in advance.
 
Sheila Haas
Laboratory Supervisor
Micro Path Laboratories


 
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Re: [Histonet] Mosquito GI Tract

2009-03-19 Thread Jackie M O'Connor
More interesting - why is someone even looking at the mosquito GI tract? 
What happens in there that we need to know about?  I guess for all the 
diseases those filthy beasts carry - they must harbor viruses and bacteria 
somewhere.   Did you know that mosquitos did not exist in Hawaii until a 
little more than 100 years ago?  Durn Westerners brought them in the 
barrels of drinking water they carried on their ships.   Welcome to 
paradise.   Oh - they also brought measles.  Thanks a lot. 





Merced Leiker lei...@buffalo.edu 
Sent by: histonet-boun...@lists.utsouthwestern.edu
03/19/2009 02:11 PM

To
Breeden, Sara sbree...@nmda.nmsu.edu, 
histonet@lists.utsouthwestern.edu
cc

Subject
Re: [Histonet] Mosquito GI Tract






lol...I wanted to say the same thing...and how in the world can you even 
see it when you section it? How do you stain it without losing it from the 

slide? Is there really enough surface area for it to adhere and withstand 
washing? ...and it's ALMOST Friday...!

--On Thursday, March 19, 2009 12:09 PM -0600 Breeden, Sara 
sbree...@nmda.nmsu.edu wrote:

 And here I thought I had an unusual project today, finding out as I did
 that my boss is thinking of examining up to 1000 cattle for TB (at 10
 lymph nodes/beast) using AFB and asking me to cost it for him.  I think
 the Mosquito GI Tract Processing and Embedding question has my project
 beat!  How would you even KNOW you had the darned GI tract to begin
 with?   Are these Texas Mosquitos?  I'm just sayin'...



 Sally Breeden, HT(ASCP)

 NM Dept. of Agriculture

 Veterinary Diagnostic Services

 PO Box 4700

 Albuquerque, NM  87106

 505-841-2576



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Merced M Leiker
Research Technician II
354 Biomedical Research Building
School of Medicine and Biomedical Sciences
State University of New York at Buffalo
3435 Main St, Buffalo, NY 14214
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[Histonet] Fluoro Jade Query

2009-03-19 Thread Jackie M O'Connor
What's the latest and greatest on Fluoro Jade for degenerating neurons? 
I've found a few references, but they are old - - so am I - just 
celebrated my birthday - - - - anyway - -who's got the best answer? Winner 
gets a Hershey Bar!

Jackie

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[Histonet] Looking for Darcy Peat

2009-03-10 Thread Jackie M O'Connor
I worked with Darcy in Hawaii years ago, and I think someone said she may 
have moved to Washington State.  Darcy, are you out there?  Does anyone 
know where she is?

Jackie O'
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Re: [Histonet] CD31 on FFPE mouse tissue

2009-02-13 Thread Jackie M O'Connor
Biocare Medical is supposed to have a good CD31 for FFPE mouse.   I don't 
have proof of this, but I would contact Biocare.





Kim Merriam kmerriam2...@yahoo.com 
Sent by: histonet-boun...@lists.utsouthwestern.edu
02/13/2009 12:27 PM
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kmerriam2...@yahoo.com


To
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cc

Subject
[Histonet] CD31 on FFPE mouse tissue






What is everyone doing for CD31 on FFPE mouse tissue?  We are looking to 
do IF, but a DAB protocol would be just as good.
 
Thanks,
Kim

Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA


 
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[Histonet] Off topic - professional licenses.

2009-02-11 Thread Jackie M O'Connor
Wow.  My last hair stylist/colorist and I obviously did not share the same 
vision of what my hair should look like.   I wonder what governing body 
licenses hairdressers, and what is the criteria?  How many of them have 
college?  Soon in Illinois you will have to have a license to breed 
dogs, but you can still be a histotech without one.People should have 
licenses before they have a child - or 14.
Flaming and it's only Wednesday.

Jackie O'





Horn, Hazel V hor...@archildrens.org 
Sent by: histonet-boun...@lists.utsouthwestern.edu
02/11/2009 11:13 AM

To
Breeden, Sara sbree...@nmda.nmsu.edu, 
histonet@lists.utsouthwestern.edu
cc

Subject
RE: [Histonet] Uncertified Techs






I'm fairly certain all hair dressers are licensed.

Hazel Horn
Hazel Horn, HT/HTL (ASCP)
Supervisor of Histology
Arkansas Children's Hospital
1 Children's WaySlot 820
Little Rock, AR   72202
 
phone   501.364.4240
fax501.364.3155
 
visit us on the web at:www.archildrens.org
 
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Breeden,
Sara
Sent: Wednesday, February 11, 2009 11:11 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Uncertified Techs

Strangely enough (but not entirely unexpectedly), beauticians and
barbers in this State must be licensed.  Histotechs? Nope.

Sally Breeden, HT(ASCP)
NM Dept. of Agriculture
Veterinary Diagnostic Services
PO Box 4700
Albuquerque, NM  87106
505-841-2576


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Re: [Histonet] Legal Question

2009-01-23 Thread Jackie M O'Connor
Or you can just ask the supplier to take it back.





Jessica Piche jessgro...@yahoo.com 
Sent by: histonet-boun...@lists.utsouthwestern.edu
01/23/2009 11:38 AM

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[Histonet] Legal Question








Hi, We have an antibody that we ordered in error. We would like to see if 
another lab would like to purchase it from us. Is that legal to ask this 
on the Histonet? Thanks!
 

Jessica Piche-Grocki, HT(ASCP)
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Re: [Histonet] prion contaminated tissue processing

2009-01-15 Thread Jackie M O'Connor
Viable prions have been found in 20 year old paraffin blocks.Only 
extended exposure to bleach will kill 'em - last I heard.   Not formalin, 
not processing - nothin. 

Jackie O'



Rene J Buesa rjbu...@yahoo.com 
Sent by: histonet-boun...@lists.utsouthwestern.edu
01/15/2009 11:32 AM
Please respond to
rjbu...@yahoo.com


To
histonet@lists.utsouthwestern.edu, Joe Hardin har...@oncology.wisc.edu
cc

Subject
Re: [Histonet] prion contaminated tissue processing






NO, it will not.
René J.

--- On Thu, 1/15/09, Joe Hardin har...@oncology.wisc.edu wrote:

From: Joe Hardin har...@oncology.wisc.edu
Subject: [Histonet] prion contaminated tissue processing
To: histonet@lists.utsouthwestern.edu
Date: Thursday, January 15, 2009, 10:29 AM

Hi All,
Does anyone know if tissue processing for paraffin embedding will render 
prion
infected tissue safe for sectioning?
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RE: [Histonet] H-QIP - spleens

2009-01-06 Thread Jackie M O'Connor
OK - my question is - - what in the heck do you need to examine the ENTIRE 
spleen for that would require breadloafing the whole thing for fixation?  
I was in hospital histology for a couple hundred years, and as I recall in 
my feeble, senility- prone years, most of the spleens that made it to 
pathology were from trauma.   The only time I've ever seen pathology in a 
spleen was when my dog had a primary splenic tumor (he died).  Is there 
some new anomaly that happens in spleens these days that require the 
entire spleen to be examined?
Just curious.
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Re: [Histonet] Sakura tape problem

2008-11-21 Thread Jackie M O'Connor
I would remove the tape with acetone and clear in xylene, then recoverslip 
with conventional coverslips.  I've seen problems with refractivity with 
the tape, anyway.

Happy Turkey Day.

Jackie O'



Cheryl Crowder [EMAIL PROTECTED] 
Sent by: [EMAIL PROTECTED]
11/21/2008 01:20 PM

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Subject
[Histonet] Sakura tape problem






Hi - I have just been given a box (100 slides) cover slipped with Sakura 
tape.  All the tapes have been loosened from the slides with the tissue 
attacked to it.  The tape has also curled (arched).  What is the best 
method 
for reattaching the tapes to the slides so they can be viewed again.  Or 
can 
it?  The pathologists are really upset over these slides as they are for 
continuing education and cannot be replaced. 
Cheryl
 
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinary Medicine
Louisiana State University
Skip Bertman Drive
Baton Rouge, LA 70803

225-578-9734
FAX: 225-578-9720
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RE: [Histonet] Sakura tape problem

2008-11-21 Thread Jackie M O'Connor
Ah - sorry, didn't read that well.  Nevermind. 





Weems, Joyce [EMAIL PROTECTED] 
11/21/2008 01:36 PM

To
Jackie M O'Connor Jackie.O'[EMAIL PROTECTED], Cheryl Crowder 
[EMAIL PROTECTED]
cc
[EMAIL PROTECTED], Histonet 
[EMAIL PROTECTED]
Subject
RE: [Histonet] Sakura tape problem






How do you do this with the tissue attached to the tape? Just curious...
j 

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Jackie M
O'Connor
Sent: Friday, November 21, 2008 2:32 PM
To: Cheryl Crowder
Cc: [EMAIL PROTECTED]; Histonet
Subject: Re: [Histonet] Sakura tape problem

I would remove the tape with acetone and clear in xylene, then
recoverslip with conventional coverslips.  I've seen problems with
refractivity with the tape, anyway.

Happy Turkey Day.

Jackie O'



Cheryl Crowder [EMAIL PROTECTED] Sent by:
[EMAIL PROTECTED]
11/21/2008 01:20 PM

To
Histonet [EMAIL PROTECTED] cc

Subject
[Histonet] Sakura tape problem






Hi - I have just been given a box (100 slides) cover slipped with Sakura
tape.  All the tapes have been loosened from the slides with the tissue
attacked to it.  The tape has also curled (arched).  What is the best
method for reattaching the tapes to the slides so they can be viewed
again.  Or can it?  The pathologists are really upset over these slides
as they are for continuing education and cannot be replaced. 
Cheryl
 
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinary Medicine
Louisiana State University
Skip Bertman Drive
Baton Rouge, LA 70803

225-578-9734
FAX: 225-578-9720
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Re: AW: [Histonet] Control slide storage

2008-11-20 Thread Jackie M O'Connor
CD31 for sure.  I do recall most surface markers I used tended to be 
unstable.

Jackie O'



Gudrun Lang [EMAIL PROTECTED] 
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11/20/2008 09:17 AM
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AW: [Histonet] Control slide storage






Hi Patsy,
I am interested in the names of this certain epitopes, that loose
stainability after long time storage.

And I'd like to ask all the other listmembers about their experiences with
this issue. Perhaps we can make a list of dangerous epitopes.

Regards
Gudrun Lang

Akh Linz, Austria

-Ursprüngliche Nachricht-
Von: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] Im Auftrag von Patsy
Ruegg
Gesendet: Donnerstag, 20. November 2008 15:09
An: [EMAIL PROTECTED];
histonet@lists.utsouthwestern.edu
Betreff: RE: [Histonet] Control slide storage

I store all cut paraffin sections for IHC control at 4dc and without 
heating
to melt the paraffin, even with that I have seen some loss of antigenicity
over long periods of time for certain antibodies.

Patsy

Patsy Ruegg, HT(ASCP)QIHC
IHCtech
12635 Montview Blvd. #215
Aurora, CO 80045
720-859-4060
fax 720-859-4110
[EMAIL PROTECTED]
www.ihctech.net
www.ihcrg.org 
 


-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of
[EMAIL PROTECTED]
Sent: Wednesday, November 19, 2008 2:31 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Control slide storage

The issue was brought up in the lab regarding the storing of IHC control 
slides. What experience has anyone had on the effects of long term storage 

and staining quality. We store the slides non preheated (with the paraffin 

still on them). 


Cindy J Chard-Bergstrom
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Re: [Histonet] RE: Leica Slide Writer

2008-11-20 Thread Jackie M O'Connor
We label tens of  thousands of slides a year - no paper labels required. I 
visited a research lab in Germany - they labele 1,000 slides a day. Never 
had a problem with the ink coming off or disappearing - where would it go?





Patricia Karlisch [EMAIL PROTECTED] 
Sent by: [EMAIL PROTECTED]
11/20/2008 12:10 PM

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Subject
[Histonet] RE: Leica Slide Writer






Just out of curiosity.  When the slide writer is working okay, do you 
still have to place paper labels on the slides or does the ink disappear 
with time??? 
Thank you,
Pat
 
Pat Karlisch
Supervisor, Histology, Pathology and Laboratory Medicine
Penn State Milton S. Hershey Medical Center
Mail Code H179
Hershey, PA 17033
Phone (717) 531-6072
Fax: (717) 531- 7741
email: [EMAIL PROTECTED] 
 
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RE: [Histonet] breast bx processing

2008-11-17 Thread Jackie M O'Connor
How long are they in molten paraffin





Angela Bitting [EMAIL PROTECTED] 
Sent by: [EMAIL PROTECTED]
11/17/2008 02:27 PM

To
Michele Margiotta [EMAIL PROTECTED], Gary Martin 
[EMAIL PROTECTED], [EMAIL PROTECTED]
cc

Subject
RE: [Histonet] breast bx processing






We have staff in on Sunday afternoon, so we start them Friday night and 
let them sit in paraffin until the techs come in on Sunday. The extra 
paraffin has actually cut down the number of dry outs we were having.

 Martin, Gary [EMAIL PROTECTED] 11/17/2008 2:14 PM 
We come in and process them ! 

-Original Message-
From: [EMAIL PROTECTED] 
[mailto:[EMAIL PROTECTED] On Behalf Of
Margiotta, Michele
Sent: Monday, November 17, 2008 9:37 AM
To: [EMAIL PROTECTED] 
Subject: [Histonet] breast bx processing

Hi All,

We are trying to figure out how to adjust our processing schedule for
breast core bxs on the weekends so that they are not sitting
in formalin for too long.  Just wondering what everyone else is doing.
Your input would be very helpful.  Thanks! 

Michele Margiotta
BMHMC
Histology Supervisor
631-654-7192




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Re: [Histonet] old electron microscopes

2008-11-14 Thread Jackie M O'Connor
Could you imagine these things on Ebay?




Joe [EMAIL PROTECTED] 
Sent by: [EMAIL PROTECTED]
11/14/2008 11:21 AM

To
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Subject
[Histonet] old electron microscopes






A freind askded me to post this question to the list and see if he could 
get
any guidance.  He has two electron microscopes that appear to this 
untrained
eye to be older than the hills, or quite possibly alien artifacts.  One is 
a
Siemens unit (power supply is bigger than a fridge).  The other, I believe
is also a siemens unit, but it appears newer (relatively), than the other.
It's a bit smaller and has an orange body to the tube part.  He wants to 
get
rid of them and wants to know if they have any value on today's market?  I
tried the histoauction, but the page did not seem be working.  Any help
would be appreciated.
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Re: [Histonet] 4 Day Weekend

2008-11-12 Thread Jackie M O'Connor
If it's antigenicity you're concerned with (we had a 48 hour max fix time) 
- set your processor to transfer the tissues to 70% alcohol and hold them 
there until time to process for Monday a.m.
Ta-daa!




Cindy DuBois [EMAIL PROTECTED] 
Sent by: [EMAIL PROTECTED]
11/12/2008 01:44 PM

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Subject
[Histonet] 4 Day Weekend






For the first time in my histo career, our lab will be closed the day 
after
Thanksgiving.  I am concerned about tissue sitting in the processors (in
formalin) for that long.  What are other labs doing?

Cindy DuBois
Integrated Pathology
Stockton, CA
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Re: [Histonet] RE: Is it Formalin-Without Smelling It?

2008-11-07 Thread Jackie M O'Connor
Years ago, we added methyl violet to our formalin which enabled us to 
quickly identify the solution in or out of a container.  It also serves as 
a pH indicator, turns yellow when acidic.  That came in handy for long 
term fixation of large bloody specimens that might have required a 
formalin change to ensure good fixation.





JR R [EMAIL PROTECTED] 
Sent by: [EMAIL PROTECTED]
11/07/2008 02:21 PM

To
histonet@lists.utsouthwestern.edu
cc

Subject
[Histonet] RE: Is it Formalin-Without Smelling It?








My favorite method is to have the container LABELED.

Jerry Ricks
Research Scientist
University of Washington
Department of Pathology



 From: [EMAIL PROTECTED]
 To: [EMAIL PROTECTED]; histonet@lists.utsouthwestern.edu
 Date: Fri, 7 Nov 2008 13:34:43 -0600
 CC: 
 Subject: [Histonet] RE: Is it Formalin-Without Smelling It?
 
 I knew there was a trick, I just couldn't remember what it was.
 Thanks everyone!
 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
 
 -Original Message-
 From: [EMAIL PROTECTED] 
[mailto:[EMAIL PROTECTED] On Behalf Of Charles, 
Roger
 Sent: Friday, November 07, 2008 1:43 PM
 To: Smith Wanda; Histonet (histonet@lists.utsouthwestern.edu)
 Subject: [Histonet] RE: Is it Formalin-Without Smelling It?
 
 We are using Shiffs reagent.  When you put a drop of formalin in Shiffs 
reagent it turns purple.
 
 Roger Charles
 Microbiologist
 Pennsylvania Veterinary Laboratory
 2305 N Cameron St
 Harrisburg, PA 17110
 717-787-8808
 
 -Original Message-
 From: [EMAIL PROTECTED] 
[mailto:[EMAIL PROTECTED] On Behalf Of Smith 
Wanda
 Sent: Friday, November 07, 2008 1:31 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Is it Formalin-Without Smelling It?
 
 Happy Friday Everyone!
 Silly question:  Is there an easy way to tell if a solution in a 
container is/is not formalin without smelling it?
 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] embedding

2008-11-06 Thread Jackie M O'Connor
2-3  hours.





KELLY BOYD [EMAIL PROTECTED] 
Sent by: [EMAIL PROTECTED]
11/06/2008 12:25 PM
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Subject
[Histonet] embedding






Just trying to get some feedback on how much time (estimated) it should 
take an average histotech with experience to embed 150 shave biopsies. Let 
us just say the majority have multiple pieces to be embeded on edge. Any 
clue?


Kelly D. Boyd, BS, HTL (ASCP)
Lab Manager
Harris Histology Services
2025 Eastgate Dr. Ste. F
Greenville, NC 27858
www.harrishisto.com 
 
Tele (252)-830-6866
Cell  (252)-943-9527
Fax  (252)-830-0032
 
 


 
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RE: [Histonet] progressive HE staining using Gills

2008-10-30 Thread Jackie M O'Connor
Richard Allen 7211 Hematoxylin doesn't stain mucin blue, and is a 
beautiful all around nuclear stain.I'm sure they'll send you a sample.





Mickie Johnson [EMAIL PROTECTED] 
Sent by: [EMAIL PROTECTED]
10/30/2008 02:16 PM
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histonet@lists.utsouthwestern.edu
cc

Subject
RE: [Histonet] progressive HE staining using Gills






Angela,

Were you using Harris before? If so, the difference is that Gill
formulations stain the mucin of goblet cells quite a dark blue and many GI
docs don't like that look. They can get used to it though as ours did at
Sacred Heart Medical Center. Hope this helps.

Best Regards,
 
Mickie
 
Mickie Johnson, B.S., HTL(ASCP)
Mohs Histology Consulting Services, LLC
   Mohs Lab Staffing
2507 S. Manito Blvd.
Spokane, WA 99203
509-954-7134
FAX   509-624-3926
Web: www.mohshistogyconsulting.com  www.mohslabstaffing.com 
Email: [EMAIL PROTECTED]
 
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-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Angela
Bitting
Sent: Thursday, October 30, 2008 11:30 AM
To: histonet
Subject: [Histonet] progressive HE staining using Gills

We just switched our HE stain to a progressive stain using Gill II
hematoxylin. Our derm guys love it, but now our GI docs are screaming 
bloody
murder. Does anyone have suggestions for a protocol that will make both
'relatively happy'?? Thanks for letting me pick your brains again!!!



Angela Bitting, HT(ASCP)
Technical Specialist, Histology
Geisinger Medical Center 
100 N Academy Ave. MC 23-00
Danville, PA 17822
phone  570-214-9634
fax  570-271-5916 
 
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RE: [Histonet] Protect fingers during Microtomy

2008-10-28 Thread Jackie M O'Connor
My Dad was a workman's comp expert for a large insurance company.   In the 
early 90's, I was managing a histo lab where the head pathologist (funny, 
a neuropath) thought it would be cheaper to resharpen stainless steel 
microtome knives instead of using disposable blades.(I had a previous 
nasty injury from a steel knife).   Dad put together an estimate on each 
individual finger of how much $$ the hospital would have to pay out in the 
event of major lacerations or amputation.  We also included feet - since 
those heavy knives would often hit the floor when you had to jump out of 
the way if someone mishandled one.   Turned out, we never used stainless 
steel knives again.It was cheaper to use disposables than for one 
person to lose the use of a thumb.
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Re: [Histonet] Toluene vs. Xylene

2008-10-09 Thread Jackie M O'Connor
Yeah - but since Toluene is the major component of airplane glue- at least 
you'll be happier using toluene over xylene. 

Jackie





Rene J Buesa [EMAIL PROTECTED] 
Sent by: [EMAIL PROTECTED]
10/09/2008 09:38 AM
Please respond to
[EMAIL PROTECTED]


To
histonet@lists.utsouthwestern.edu, James Dooley [EMAIL PROTECTED]
cc

Subject
Re: [Histonet] Toluene vs. Xylene






Not really and both are as dangerous and both should be avoided. As a 
matter of fact xylene began to be used in the mid 1950s to substitute 
chemicals like toluene, until it was found that both were equally 
dangerous. Toluene is present in many mounting media.
René J.

--- On Thu, 10/9/08, James Dooley [EMAIL PROTECTED] wrote:

From: James Dooley [EMAIL PROTECTED]
Subject: [Histonet] Toluene vs. Xylene
To: histonet@lists.utsouthwestern.edu
Date: Thursday, October 9, 2008, 10:16 AM

Is there a significant difference between using xylene and toluene when
deparaffinizing embedding tissue?

Thank you, 
James



 
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