Re: [Histonet] Histopathology text recommendations

2018-05-21 Thread Esther C Peters via Histonet
Hi Gordon,


I think you meant a histopathology atlas for slide reading, right? I am not a 
human histopathologist, but there are many such texts available, for example, 
see these at Amazon:


https://www.amazon.com/s/ref=nb_sb_noss_1?url=search-alias%3Dstripbooks&field-keywords=histopathology

Amazon.com: histopathology: 
Books<https://www.amazon.com/s/ref=nb_sb_noss_1?url=search-alias%3Dstripbooks&field-keywords=histopathology>
www.amazon.com
Online shopping from a great selection at Books Store.

Also, several websites from medical schools offer virtual microscopy histoslide 
collections of different pathologies, such as:


https://med.virginia.edu/biomolecular-analysis-facility/services/shared-instrumentation/aperio-scanscope-slide-scanner/catalogs-of-histology-and-pathology-virtual-slides-on-the-web/


<https://med.virginia.edu/biomolecular-analysis-facility/services/shared-instrumentation/aperio-scanscope-slide-scanner/catalogs-of-histology-and-pathology-virtual-slides-on-the-web/>http://www.mbfbioscience.com/iowavirtualslidebox


<https://med.virginia.edu/biomolecular-analysis-facility/services/shared-instrumentation/aperio-scanscope-slide-scanner/catalogs-of-histology-and-pathology-virtual-slides-on-the-web/>https://www.amboss.com/us/knowledge/Virtual_histopathology_slide_box


And others, just search in Google for "histopathology virtual slide box."


Perhaps one of the pathologists on this list-serv can guide you to the best 
one(s) for your needs!


Esther


Esther C. Peters, Ph.D.
Term Associate Professor
Environmental Science & Policy
George Mason University
4400 University Drive, MS 5F2
Fairfax, VA 22030-
Office: David King Hall, Room 3050
Phone: 703-993-3462
Fax: 703-993-1066
e-mail: epete...@gmu.edu<mailto:epete...@gmu.edu>
<https://bluprd0511.outlook.com/owa/redir.aspx?C=ET8XhF-xC0ytBErXdaN3U3lGqWmZNdAI_N-4nsEb0IjgUpeIoQa7EcVMJMh2oePPPKrrDjhwOvk.&URL=http%3a%2f%2fesp.gmu.edu>http://esp.gmu.edu


From: Frazier, John via Histonet 
Sent: Sunday, May 20, 2018 5:31:01 PM
To: Saundra Ellis
Cc: histonet@lists.utsouthwestern.edu; Gordon Brown
Subject: Re: [Histonet] Histopathology text recommendations

Histotechnology: A Self-Instructional Text
Sent from my iPhone

On May 19, 2018, at 5:17 PM, Saundra Ellis <
saundra.el...@floridawomancare.com> wrote:

Anything written by Freida Carson.

Saundra Ellis
Histology Supervisor
Florida Woman Care Laboratory
Cell (360) 513-9665 (best contact)
FAX (813) 433-5542

saundra.el...@floridawomancare.com



From: Gordon Brown via Histonet 
Sent: Saturday, May 19, 2018 2:49:45 PM
To: histonet@lists.utsouthwestern.edu
Cc: Gordon Brown
Subject: [Histonet] Histopathology text recommendations

Can anyone give me recommendations for a good histopathology text and
atlas? I'm not a professional or even a formal student, I'm an amateur
microscopist with a keen interest in histology, although I did attend a UK
medical school many years ago only to decide that medicine was not for me.
I'm now retired and expanding my interest in microscopy, which has
fascinated me since the age of 8, I now have a collection of decent
microscopes and microtomes and I'm setting up my study as a home microscopy
and slide making facility. I have a growing collection of old histology
slides including a number of pathology examples and I'm keen to be able to
identify the histological changes that take place due to disease. In
particular I am looking to be able to identify and photograph carcinomas as
I recently acquired a photomicrography bench used by the Imperial Cancer
Research Campaign in London during the 1950s and 1960s, and it would be
appropriate to use it for the purpose it was designed for.

Hope someone can help, I've subscribed to this list for many years but only
rarely posted anything, the last time was when I enquired about replaceable
blade holders for the original Cambridge rocking microtome and a very kind
histologist in the USA sent me a slightly damaged holder and some blades.
Fortunately I never managed to adapt it for the Cambridge as it is a
perfect fit for the Reichert and Leitz rotary microtomes I now own!
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[Histonet] Weigert's hematoxylin for IHC

2016-11-22 Thread Esther C Peters via Histonet
Could someone advise me on whether Weigert's iron hematoxylin can be used as 
the counterstain for nuclei in IHC? We need to avoid using Harris's hematoxylin 
because that will stain mucocytes in the coral tissues we are working with. If 
it can be used, would that be after all antibody steps have been done? Thank 
you!


Esther Peters


Esther C. Peters, Ph.D.
Term Associate Professor
Environmental Science & Policy
George Mason University
4400 University Drive, MS 5F2
Fairfax, VA 22030-
Office: David King Hall, Room 3050
Phone: 703-993-3462
Fax: 703-993-1066
e-mail: epete...@gmu.edu<mailto:epete...@gmu.edu>
<https://bluprd0511.outlook.com/owa/redir.aspx?C=ET8XhF-xC0ytBErXdaN3U3lGqWmZNdAI_N-4nsEb0IjgUpeIoQa7EcVMJMh2oePPPKrrDjhwOvk.&URL=http%3a%2f%2fesp.gmu.edu>http://esp.gmu.edu

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[Histonet] For sale: Lab storage - Tissue-Tek flat tray cases

2015-09-03 Thread Esther C Peters via Histonet
Tissue-Tek slide storage tray case. Capacity is 800 slides (50 trays of 16 
slides each). These are hard to find in the US - model #4023. Slides store 
flat. Have 12 brand new still in boxes. $180 each.  (703)342-7804 or 
katca...@ymail.com

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Re: [Histonet] Handline paraffin

2015-08-03 Thread Esther C Peters via Histonet
However, I would be concerned if using Paraplast Plus (+) because it contains 
dimethyl sulfoxide (DMSO) to infiltrate the tissue faster. It can be absorbed 
through bare skin and you get a garlic taste in your mouth, making you wonder 
what else was absorbed into your body (DMSO is used for transdermal drug 
administration). We wear gloves when working with molten Paraplast +, but not 
for microtomy of the solidified blocks.

Esther

Esther C. Peters, Ph.D.
Term Associate Professor
Environmental Science & Policy
George Mason University
4400 University Drive, MS 5F2
Fairfax, VA 22030-
Office: David King Hall, Room 3050
Phone: 703-993-3462
Fax: 703-993-1066
e-mail: epete...@gmu.edu
https://bluprd0511.outlook.com/owa/redir.aspx?C=ET8XhF-xC0ytBErXdaN3U3lGqWmZNdAI_N-4nsEb0IjgUpeIoQa7EcVMJMh2oePPPKrrDjhwOvk.&URL=http%3a%2f%2fesp.gmu.edu



From: Rene J Buesa via Histonet 
Sent: Monday, August 3, 2015 12:52 PM
To: Johnson, Carole; histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Handline paraffin

It is absolutely NOT necessary to wear gloves when working with paraffin. This 
is NOT a harmful or "irritating" substance. It is just an oil of high molecular 
weight (mineral oil)René


 On Monday, August 3, 2015 12:48 PM, "Johnson, Carole via Histonet" 
 wrote:


 This is kind of an odd question, but I was asked by a pathologist for any SOPs 
or references for the necessity of wearing gloves when embedding and working 
with paraffin. I am not aware of sources other than the MSDS for the different 
formulations. Does anyone require gloves to be worn during embedding, 
specifically related to paraffin hazards?

Carole Johnson
Carole Johnson, HT(ASCP)cm
New Mexico Department of Agriculture
Veterinary Diagnostic Services
505.383.9299

To understand is to stand under, which is to look up, which is a good way to 
understand




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[Histonet] Re: Cutting of Paraffin Blocks

2015-03-25 Thread Esther C Peters
I start my students with plain paraffin blocks (no tissue in them) that they 
make themselves, to start. After they have worked with those, looking at how 
adjustments, then icing, then moving sections to the waterbath work, then I 
give them old practice blocks. This seems to be less intimidating than starting 
with tissue (although I think that is how I learned!).

Esther C. Peters, Ph.D.
Term Associate Professor
Environmental Science & Policy
George Mason University
4400 University Drive, MS 5F2
Fairfax, VA 22030-
Office: David King Hall, Room 3050
Phone: 703-993-3462
Fax: 703-993-1066
e-mail: epete...@gmu.edu
https://bluprd0511.outlook.com/owa/redir.aspx?C=ET8XhF-xC0ytBErXdaN3U3lGqWmZNdAI_N-4nsEb0IjgUpeIoQa7EcVMJMh2oePPPKrrDjhwOvk.&URL=http%3a%2f%2fesp.gmu.edu



From: histonet-boun...@lists.utsouthwestern.edu 
 on behalf of Cooper, Brian 

Sent: Wednesday, March 25, 2015 1:17 PM
To: Laurie Colbert; Adesupo, Adesuyi (Banjo); 
'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] RE: Cutting of Paraffin Blocks

Completely agree.  Give them practice tissue blocks because it's expected that 
they WILL destroy them during the early stages of their learning process.

If I can go one further here--when these students have demonstrated acceptable 
microtomy technique (and when you feel comfortable), be sure to teach them how 
to realign their microtome's orientation head/specimen clamp to the surface of 
blocks that have been previously cut.I cannot tell you how many histotechs 
I've met in my career who didn't possess this skill and simply "refaced" these 
blocks.   One even yelled at the Biomedical Maintenance tech when he serviced 
her microtome and readjusted the orientation!

I have a student in our lab right now, and tasked her with providing me 5 H&E's 
from each of the practice blocks I gave her.  Here's the catch.  In between 
each section that she collects, she is supposed to completely misalign the 
specimen head, then realign to the surface of the block.  I told her that all 
five H&E's from each block should look relatively similar by the time she's 
done, and that there should be no appreciable tissue loss.  While this might 
seem like a torture test for beginners, it will only serve them (and ultimately 
the patients they serve) so well in the future.

Thanks,

Brian D. Cooper, HT (ASCP)CM | Histology Supervisor
Department of Pathology and Laboratory Medicine
Children's Hospital Los Angeles
4650 Sunset Blvd MS#43- Los Angeles, CA 90027
Ph: 323.361.3357 Pager: 213-209-0184
bcoo...@chla.usc.edu

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Laurie Colbert
Sent: Wednesday, March 25, 2015 9:49 AM
To: Adesupo, Adesuyi (Banjo); 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] RE: Cutting of Paraffin Blocks

Heck no, crack that whip!  Give them practice tissue that isn't important so 
they won't be afraid of ruining something.

Laurie Colbert, HT (ASCP)

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Adesupo, 
Adesuyi (Banjo)
Sent: Wednesday, March 25, 2015 9:26 AM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] Cutting of Paraffin Blocks

Hi,
   How are you guys doing? I hope you are all doing well. Please  I have two 
histology trainees and  they have spent more than six months in the histology 
lab and they cannot cut blocks yet. They are comfortable with filing slides and 
blocks.
But I have been telling them that they have to start cutting now. My question 
now is am I too hard on them?

Best regards,
Adesupo Adesuyi
==
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[Histonet] Re: Recycling alcohol

2015-01-20 Thread Esther C Peters
American Mastertech Scientific makes Reagent Alcohol with just ethanol and 
isopropanol. 

Esther C. Peters, Ph.D.
Term Associate Professor
Environmental Science & Policy
George Mason University
4400 University Drive, MS 5F2
Fairfax, VA 22030-
Office: David King Hall, Room 3050
Phone: 703-993-3462
Fax: 703-993-1066
e-mail: epete...@gmu.edu
https://bluprd0511.outlook.com/owa/redir.aspx?C=ET8XhF-xC0ytBErXdaN3U3lGqWmZNdAI_N-4nsEb0IjgUpeIoQa7EcVMJMh2oePPPKrrDjhwOvk.&URL=http%3a%2f%2fesp.gmu.edu



From: histonet-boun...@lists.utsouthwestern.edu 
 on behalf of Marcum, Pamela A 

Sent: Tuesday, January 20, 2015 9:22 AM
To: Horn, Hazel V; 'Vickroy, James'; histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: Recycling alcohol

Hazel is correct if you use the pure ethanol the paperwork is horrible and the 
limits on what should be in the lab are very low for a normal Histology Lab.  
Reagent alcohol is the best way to go as it has methanol and isopropanol in it 
so it is undrinkable and therefore not under the same ATF rules of usage.

Pam Marcum
UAMS

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Horn, Hazel V
Sent: Monday, January 19, 2015 1:05 PM
To: 'Vickroy, James'; histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: Recycling alcohol

With Ethyl alcohol you will need a license and will have to keep records.  With 
reagent grade alcohol none of that is necessary.

Hazel Horn
Supervisor of Histology/Autopsy/Transcription Anatomic Pathology Arkansas 
Children's Hospital
1 Children's Way | Slot 820| Little Rock, AR 72202
501.364.4240 direct | 501.364.1241 fax
hor...@archildrens.org
archildrens.org





-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Vickroy, James
Sent: Monday, January 19, 2015 12:28 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Recycling alcohol

We are planning to recycle alcohol in the new lab I am working with.   
Previously I always used an alcohol blend such as the "Flex" products.  However 
at this new lab we are going to only process biopsies so I believe I can get by 
using ethanol and not a blend.   We will be getting our alcohol from 
Thermofisher.  Can anyone tell me which alcohols they are using for 
dehydration?  Reagent alcohol or ethyl alcohol.  Obviously we will make our own 
concentrations from a 100%.

Jim

Jim Vickroy
Histology Manager
Springfield Clinic, Main Campus, East Building
1025 South 6th Street
Springfield, Illinois  62703
Office:  217-528-7541, Ext. 15121
Email:  jvick...@springfieldclinic.com<mailto:jvick...@springfieldclinic.com>


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Conf

[Histonet] Anyone doing insect histology?

2014-10-31 Thread Esther C Peters
?Do any of you do insect histology/histopathology? We are looking for someone 
to process the insects (primarily bees) and then read the histoslides and 
provide a report on the findings. Appreciate any assistance you can provide, or 
potential contacts!


Esther C. Peters, Ph.D.
Term Associate Professor
Environmental Science & Policy
George Mason University
Fairfax, VA 22030-
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[Histonet] RE: paraffin

2014-08-13 Thread Esther C Peters
The nice thing about those is that "sticky mats" will also collect the dust 
from shoes; I found that these stop a lot of dust coming in at the outside door 
entrances, as well as having them to collect paraffin under the embedding 
center, in front of the tissue processor and fume hoods, and under the 
microtomes. It is amazing how much dust and dirt can come in with people's  
shoes!

Esther C. Peters, Ph.D.
Associate Professor
Environmental Science & Policy
George Mason University
4400 University Drive, MS 5F2
Fairfax, VA 22030-
Office: David King Hall, Room 3050
Phone: 703-993-3462
Fax: 703-993-1066
e-mail: epete...@gmu.edu
https://bluprd0511.outlook.com/owa/redir.aspx?C=ET8XhF-xC0ytBErXdaN3U3lGqWmZNdAI_N-4nsEb0IjgUpeIoQa7EcVMJMh2oePPPKrrDjhwOvk.&URL=http%3a%2f%2fesp.gmu.edu



From: histonet-boun...@lists.utsouthwestern.edu 
 on behalf of Walter Benton 

Sent: Wednesday, August 13, 2014 9:05 PM
To: Algeo, Lacie A; histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: paraffin

You may want to purchase the large tack mats for staff to walk over when going 
in and out of your embedding area. These come in blue, white, or gray:
http://www.fishersci.com/ecomm/servlet/itemdetail?storeId=10652&langId=-1&catalogId=29104&productId=5264212&distype=0&highlightProductsItemsFlag=Y&fromSearch=1&searchType=PROD&hasPromo=0



Walter Benton HT(ASCP)QIHC
Histology Supervisor
Chesapeake Urology Associates
806 Landmark Drive, Suite 127
Glen Burnie, MD 21061
443-471-5850 (Direct)
410-768-5961 (Lab)
410-768-5965 (Fax)
Chesapeakeurology.com

Voted a Best Place to Work by
Baltimore and Modern Healthcare
Magazines.

From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Algeo, Lacie A 
[lacie.al...@providence.org]
Sent: Wednesday, August 13, 2014 6:24 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] paraffin

Hi all,
I am dealing with an issue with slippery floors outside of our Histology 
department.  The concern is that it is from paraffin scraps tracked on the 
bottoms of peoples shoes.  The floor is cleaned every night and an anti-slip 
agent applied.  I have tested whether our paraffin makes the floors more 
slippery and it actually makes it harder to slipalmost tacky.  I really do 
not think it is our paraffin.  I think it is a thin layer of dust that settles 
on the floors after they are cleaned.  I have seen this happen in other places. 
 Is anyone dealing with this?  Any insight?
Thanks,
Lacie

Lacie Algeo, HTL (ASCP) MBCM
Histology Supervisor
Providence Sacred Heart Medical Center Laboratory
101 W 8th Avenue
L-2
Spokane, WA 99204
509-474-4418
FAX 509-474-2052
lacie.al...@providence.org<mailto:lacie.al...@providence.org>


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RE: [Histonet] HTL certification

2014-05-19 Thread Esther C Peters
Hi C.A.,

I don't have the HT or HTL, but from my college teaching experience in 
histology and histotechniques, I just wanted to caution you that memorizing is 
not what you should be doing. You need to understand concepts, so that when you 
need to troubleshoot problems you will be able to think through things, rule 
some things out, and make sense of the situation. I see this all the time with 
my students, they forget things they memorize, but then they finally understand 
things and can figure things out. One of the new teaching tools is having 
students prepare "concept maps," to see the relationships of topics and terms, 
and these linkages will help you in the long run. For histology examples, see: 
http://www.biologycorner.com/anatomy/tissues/tissue_concept_map_samples.html

I don't know of any concept maps for histotechnology on the web, but I am going 
to add this to my course next year!

Esther

Esther C. Peters, Ph.D.
Assistant Professor
Environmental Science & Policy
George Mason University
4400 University Drive, MS 5F2
Fairfax, VA 22030-
Office: David King Hall, Room 3050
Phone: 703-993-3462
Fax: 703-993-1066
e-mail: epete...@gmu.edu
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From: histonet-boun...@lists.utsouthwestern.edu 
 on behalf of Cecy Stan 

Sent: Monday, May 19, 2014 1:32 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] HTL certification

Hello everyone,

I'm starting to prepare for my HTL certification (I am very nervous
and anxious but also very excited about this decision to go for it).

I was just curious to know how you guys prepared for it, and how long it
took for you to prepare before taking the test. Will 6 months preparation
be enough? (I know that may depend on the individual; it's just that I
had my Masters over 10 years ago and I haven't studied this much since
then).

I have Freida L. Carson's 3rd Edition book -- quite daunting to memorize --
but the outline ASCP  has provided for study seems to be helpful. Do you
have any other book/study aid suggestions?

Thank you in advance for your input and advice!
C.A.
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RE: [Histonet] Histogel

2014-01-22 Thread Esther C Peters
Thank you, John!

For some strange reason, the URL in your message got garbled/multiplied, but I 
just took this part:

http://www.thermo.com/eThermo/CMA/PDFs/Various/File_9759.pdf

and that worked.

The enrobing I do is to trap debris on the surface of a coral skeleton at the 
interface between "apparently healthy" tissue and "bare" skeleton in studying 
the tissue loss diseases of the corals. After solidifying the agarose, I decal 
the sample in neutral pH 10% EDTA, then cut ("breadloaf-style") the 
agarose-enrobed tissue block into ~2-mm slices and put each in a cassette for 
processing. Perhaps my problem is the processing time needs to be increased to 
be sure to remove all the water from the agarose and infiltrate it completely.

I don't know what the instructions mean by "non-porous filter paper," either, 
has anyone figured this out?

Esther

From: histonet-boun...@lists.utsouthwestern.edu 
 on behalf of John Kiernan 

Sent: Tuesday, January 21, 2014 8:54 PM
To: histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Histogel

The document at 
http://lists.utsouthwestern.edu/mailman/listinfo/histonet(http://www.thermo.com/eThermo/CMA/PDFs/Various/File_9759.pdf";>http://www.thermo.com/eThermo/CMA/PDFs/Various/File_9759.pdf
 gives a thorough description of Histogel, and even says what it is - 
hydroxyethyl agarose.  In the detailed instructions for various uses, the only 
confusing thing is the requirement for "non-porous filter paper"!

John Kiernan
Anatomy, UWO
London, Canada
= = =
On 20/01/14, Elizabeth Chlipala  wrote:
>  Esther
>
> I agree with Dusko, I fix before I put in histogel and again after the sample 
> is placed in histogel, we have no formalin on our tissue processor, we start 
> in 50% alcohol.  I also process on a longer processing cycle, 1 hour per 
> station and similar to Dusko's - denatured ethanol, xylene and paraplast and 
> paraplast extra to embed.  I've never had a problem (such as overprocessed 
> tissue) with the histogel or the sample embedded in the histogel with the 
> longer processing cycle.  Most of the samples we process are cell blocks or 
> tissue fragments such as micronized tissue constructs, which are like powder 
> when we receive them.
>
> Liz
>
> Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
> Premier Laboratory, LLC
> PO Box 18592
> Boulder, CO 80308
> (303) 682-3949 office
> (303) 682-9060 fax
> (303) 881-0763 cell
> l...@premierlab.com
> www.premierlab.com
>
> Ship to Address:
>
> Premier Laboratory, LLC
> 1567 Skyway Drive, Unit E
> Longmont, CO 80504
>
> -Original Message-
> From: histonet-boun...@lists.utsouthwestern.edu 
> [mailto:histonet-boun...@lists.utsouthwestern.edu] 
>  On Behalf Of dusko trajkovic
> Sent: Monday, January 20, 2014 12:47 PM
> To: Esther C Peters; jennifer.arcand-john...@genzyme.com; 
> histonet@lists.utsouthwestern.edu
> Subject: Re: [Histonet] Histogel
>
> Esther,
> I mainly process cells, which have been spun down into a small pellet. Also 
> mouse DRG's and other very small tissues. I would consider this delicate, so 
> do not be afraid to use a longer processing program. Histogel/Agurose is what 
> needs longer dehydrating steps.
> We do not use any substitute reagents, so in that aspect I cannot tell you 
> how they will affect the processing. Our lab uses ethanol, xylene, and 
> Paraplast paraffin. Try a test run and let me know if you were able to get 
> successful results.
> Have a good Monday!
> Dusko
>
>
> 
>  From: Esther C Peters 
> To: "jennifer.arcand-john...@genzyme.com" 
> ; "histonet@lists.utsouthwestern.edu" 
> ; dusko trajkovic 
> Sent: Monday, January 20, 2014 11:15 AM
> Subject: RE: [Histonet] Histogel
>
>
> Thank you, Dusko!
>
> I have had the same problem with 1.5% agarose, and I tried starting the 
> dehydration with 30% to 50% to 70% ethanol, and using different xylene 
> substitutes. It appears that the variable whitening and shrinking happens 
> after 100% reagent alcohol and in the xylene substitute (now using 
> Richard-Allan Clear-Rite3). I've wondered if slow infiltration was the issue. 
>  I guess we'll try this longer processing, but I also work with delicate 
> tissues that normally would be a short run (15 min in each reagent). Are your 
> tissues thin/delicate/biopsy or cell preps or organ samples? No effect on 
> them?
>
> Esther
>
> Esther C. Peters, Ph.D.
> Assistant Professor
> Environmental Science & Policy
> George Mason University
> 4400 University Drive, MS 5F2
> Fairfax, VA 22030-
> 
> From: histonet-boun...@li

RE: [Histonet] Histogel

2014-01-20 Thread Esther C Peters
Thank you, Dusko!

I have had the same problem with 1.5% agarose, and I tried starting the 
dehydration with 30% to 50% to 70% ethanol, and using different xylene 
substitutes. It appears that the variable whitening and shrinking happens after 
100% reagent alcohol and in the xylene substitute (now using Richard-Allan 
Clear-Rite3). I've wondered if slow infiltration was the issue.  I guess we'll 
try this longer processing, but I also work with delicate tissues that normally 
would be a short run (15 min in each reagent). Are your tissues 
thin/delicate/biopsy or cell preps or organ samples? No effect on them?

Esther

Esther C. Peters, Ph.D.
Assistant Professor
Environmental Science & Policy
George Mason University
4400 University Drive, MS 5F2
Fairfax, VA 22030-

From: histonet-boun...@lists.utsouthwestern.edu 
 on behalf of dusko trajkovic 

Sent: Monday, January 20, 2014 1:58 PM
To: jennifer.arcand-john...@genzyme.com; histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Histogel

Jennifer,
You might have seen one of my posts from 2-3 years ago. I had the exact same 
problems you described. Could not get anyone to come up with a solution. I ran 
various programs on our VIP and finally came up with a solution.
Fix your specimens as you normally would do. Drain of the fixative add your 
histogel (dissolved in hot water, which you have been doing), fill the mold 
with the histogel. Let solidify on ice or 4C in fridge. Place the solid 
histogel in a cassette and process on a 12 hour program. Since I have 
instituted this procedure, have not had one bad block to date. Longer 
processing is the answer, and nothing else.
Good Luck.
Dusko Trajkovic
Pfizer Inc. La Jolla
858-638-6202



 From: "jennifer.arcand-john...@genzyme.com" 

To: histonet@lists.utsouthwestern.edu
Sent: Monday, January 20, 2014 7:56 AM
Subject: [Histonet] Histogel


Dear Histonetters,

I have been reading up on the archives for info on Histogel.  Previous posts 
discuss how they had problems with it - some samples would come out great and 
some would shrivel up or even dissolve.
These posts on the Histogel were from a few years ago and was hoping, and 
praying that someone out there may have solved this issue and have a little 
info you could share with me on this subject.  Did anyone out there ever figure 
out how to get consistent results?
I have spoken with RA Scientific and they have no additional insights.

Here is the background:  I have used Histogel for about 4 years now.  In 
September of last year, we started seeing the shriveling Histogel samples.  
Like others who posted, it was random.  I could embed two serial pieces of 
nerve, from the same mouse, into two blocks and one would shrivel and one would 
look great.  So I have tried many things, always in multiples of 3 or more per 
condition per run...

Fixing in formalin only, embedding in Histogel and storing in PBS until 
processing
Fixing in formalin only, embedding in Histogel and storing in 40% reagent 
alcohol until processing (the first step of our processor is 40%)
Fixing in formalin only, embedding in Histogel and storing in formalin until 
processing
Fixing in formalin, rinsing in 40% alcohol, embedding in Histogel, and storing 
in 40% or formalin until processing
For all of these conditions, I have tried using a small cycle (30 min/bath) and 
a biopsy cycle (15 minutes/bath).
Once processed, there was no rhyme or reason to the results.  Some blocks 
looked great; others within the same group looked shriveled.  Sometimes the 
blocks were white, sometimes they were clear.

Next, I thought it was my pre-processing - so I heated the Histogel in a water 
bath, rather than microwaving.  That way all of the samples were embedded with 
the Histogel at the same temperature - about 55 degrees.
Again, no rhyme or reason, some looked good, some looked bad.

Lastly I thought that maybe I was carrying over too much liquid from my sample 
to the Histogel so I tried the following:
I made Histogel only blocks or added 3-4 drops of 40% alcohol or formalin to 
the liquid Histogel before a tissue/cell free block was made.
Yep, you guessed it - no luck.  Some looked good, some looked shriveled.

So here I have this great tool to embed tiny samples, but I am afraid to use it 
because I don't know if it will work or shrivel!  Can anyone out there help me?
Thanks,
Jenn


Jennifer Johnson

Staff Scientist

Genzyme, a Sanofi Company

Department of Pathology

5 Mountain Road

Framingham, MA 01701-9322

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RE: [Histonet] Shipping Slides

2013-07-31 Thread Esther C Peters
The trick to successful shipping is to make sure the slides cannot rattle in 
the slide box. If you put your tissue, gauze, or bubble wrap layer on top and 
shut the box, shake gently to see if they can move. If so, you can put a piece 
of tape across all the slides in the box to anchor them in place (stick the 
tape ends to the outside of the box. Then make sure the box is securely shut, 
putting tape or rubber bands around the outside in both directions. Then pack 
in a well-padded sturdy shipping box!

Esther C. Peters, Ph.D.
Assistant Professor
Environmental Science & Policy
George Mason University


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of Rathborne, Toni 
[trathbo...@somerset-healthcare.com]
Sent: Wednesday, July 31, 2013 11:38 AM
To: 'Debbie Granato'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Shipping Slides

If the slides are well dried, you can also bunch them together and wrap in a 
paper towel if you don't have too many. Tape when wrapped, then place in a 
slide box and insert in a padded envelope for shipping.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Debbie Granato
Sent: Wednesday, July 31, 2013 11:05 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Shipping Slides

Good Morning!

Can anyone tell me the best way that you have found to ship slides by Fed Ex?
 I need to send several cases out and want the safest way possible to eliminate 
broken slides.
We have tried plastic slide boxes with gauze for cushioning and then taped shut 
and a few other ways. Are there special transport slide containers, other than 
the 5 slide holders.
Any suggestions would be greatly appreciated!

Thank you,
Debbie Granato HT(ASCP)
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RE: [Histonet] Paraplast Xtra Melting Point?

2013-04-26 Thread Esther C Peters
I have wondered about that myself recently. Noticed lower temperature needed in 
our waterbaths and melting at lower temperature in embedding center. Shiny 
drops form on top of our blocks, but not with the tissue.

Esthr

Esther C. Peters, Ph.D.
Assistant Professor
Environmental Science & Policy
Biology Program, Medical Technology Coordinator
George Mason University


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of Marsh, Nannette 
[n...@stowers.org]
Sent: Friday, April 26, 2013 11:29 AM
To: 'Rene J Buesa'; Jones, Laura; Histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Paraplast Xtra Melting Point?

On the back of the bag are the instructions : 52 degrees melting point:  for 
best results, use at temperatures above 56 degrees.  Would it make a difference 
if it melted at the lower temperature but, embedding is done at the warmer 
temperature?   Just wondering.  Thank you for your response.
 Nanne Marsh

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rene J Buesa
Sent: Friday, April 26, 2013 8:52 AM
To: Jones, Laura; Histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Paraplast Xtra Melting Point?

The "rule of thumb" is that the lower the paraffin melting point is the higher 
the compression rate is.
It would be nice to ask the manufacturer why the change; perhaps they have 
added something that reduces the melting point, but I really do not think they 
should do that without warning the users.
René J.

From: "Jones, Laura" 
To: "Histonet@lists.utsouthwestern.edu" 
Sent: Friday, April 26, 2013 9:41 AM
Subject: [Histonet] Paraplast Xtra Melting Point?


Happy Friday to all!  For those of you who use Paraplast Xtra, had you noticed 
that the melting point printed on the bag has changed from 56 degrees to 52 
degrees?  I've seen several comments recently about problems with compression 
with this paraffin; and we have been experiencing the same problem.  A friend 
and former coworker contacted me about similar problems they are having in her 
new lab, and they had noticed the change in the melting point.  We get our 
Paraplast Xtra from Fisher, but it's difficult to say who is actually making it 
from the information on the bag.  Does anyone else have experiences to share?  
I'm uncertain if this is the cause of our compression issues, but I'm throwing 
it out there for all of you experts.  Thank you in advance!



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Re: [Histonet] RE: interview

2013-01-10 Thread Esther C Peters
In my histology class for (mostly) college seniors, I now try to emphasize 
learning those specific qualities (follow directions, pay close attention to 
detail, and communicate well), as well as the subject. It is amazing how often, 
when you specify to "label only 4 structures" or "provide 2 complete sentences 
to explain" or "follow this format in a report," students will not do this! 

Esther C. Peters, Ph.D.
Assistant Professor
Department of Environmental Science & Policy
Biology Program/Medical Technology Coordinator
George Mason University
4400 University Drive, MSN 5F2
Fairfax, VA 22030-

- Original Message -
From: "Kienitz, Kari" 
Date: Tuesday, January 8, 2013 4:10 pm
Subject: [Histonet] RE: interview

> Hi Gale,
> 
> In my career I have had the pleasure of hiring many OJT 
> histotechs.  With varying degrees of education and  a whole range 
> of personalities.  The things that tend to really stand out in the 
> candidates who excelled are the ones who could follow direction, 
> pay close attention to detail, and communicate well.  Histology is 
> a field where as many mundane tasks must be done as the 
> complicated ones. 
> 
> For many years we would administer to all final candidates a 
> simple aptitude test.  It was honestly something most 3rd graders 
> could do.  Its was amazing how many people would get caught up 
> following directions on where to place their name on the paper and 
> simple math.
> 
> 
> Kari Kienitz HT, (ASCP)
> Histology Laboratory
> Portland Gastroenterology
> The Oregon Clinic
>  NE 99th Ave
> Portland, OR  97220
> 503.935.8311
> kkien...@orclinic.com
> 
> 
> 
> 
> CONFIDENTIALITY WARNING: This e-mail and any attachments are for 
> the exclusive and confidential use of the intended recipient. If 
> you are not the intended recipient, please do not read, distribute 
> or take action in reliance upon this missive. If you have received 
> this in error, please notify the sender immediately by reply e-
> mail and delete this message and its attachments from your 
> computer system. Thank you
> 
> From: histonet-boun...@lists.utsouthwestern.edu [histonet-
> boun...@lists.utsouthwestern.edu] On Behalf Of Gale Limron 
> [ga...@unionhospital.org]Sent: Tuesday, January 08, 2013 10:02 AM
> To: histonet@lists.utsouthwestern.edu
> Subject: [Histonet] interview
> 
> Hello,
> I just found out today I will be doing 2nd interviews for 3 
> candidates for a part time Histology position at our hospital on 
> Friday of this week. These candidates are not histotechs but are 
> willing to do online training and take ASCP board exam within 24 
> months. I would appreciate some help with what questions to ask. I 
> did not attend the 1st interviews but these were done by our lab 
> manager who does not know a lot about what we do I 
> histology.Thank you!
> 
> Gale Limron CT,HT (ASCP)
> Histology Supervisor
> Union Hospital
> 659 Boulevard
> Dover, Ohio 44622
> 330-343-3311 ext 2562
> 
> 
> 
> This e-mail is intended only for the person or entity to which it 
> is addressed and may contain information that is privileged, 
> confidential or otherwise protected from disclosure. 
> Dissemination, distribution or copying of this e-mail or the 
> information herein by anyone other than the intended recipient, or 
> an employee or agent responsible for delivering the message to the 
> intended recipient, is prohibited. If you received this message in 
> error, please delete without copying and kindly e-mail a reply to 
> inform us of the mistake in 
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[Histonet] Acid-cleaning of slides for metals stains

2012-09-16 Thread Esther C Peters
We are going to do special stains for iron (Perl's Prussian Blue for ferric 
iron, Mallory's Method from WebPath: Internet Pathology Laboratory) and copper 
(Rhodanine from Carson and Hladik) in mouse livers. We have on hand unopened 
boxes of plus-charged microscope slides. Do we need to acid clean these slides 
before we put sections on them for these stains (understanding that the charge 
will no longer exist, but the cleaning is more important for these stains)?

I would also appreciate any insights about the best acid-cleaning procedure for 
all glassware for these stains. I have used nitric acid in the past, swirling 
it around the staining dishes and covering glass racks in a staining dish (how 
long should this be for?), then rinsing with double-deionized water (or would 
you recommend distilled only?). Thank you! 

Esther C. Peters, Ph.D.
Assistant Professor
Department of Environmental Science & Policy
Biology Program/Medical Technology Coordinator
George Mason University
4400 University Drive, MSN 5F2
Fairfax, VA 22030-
Office: David King Hall 3057
Phone: 703-993-3462
Fax: 703-993-1066
epete...@gmu.edu

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Re: [Histonet] Scope of Practice

2012-02-26 Thread Esther C Peters
Hi Bharti,

As Rene notes, it is "not a given" that every researcher in conservation or 
environmental science uses histology in their research, although they should! 
But, everyone is specialized these days and we can only know and apply so much; 
however, collaborations with histologists and histopathologists do occur, and 
many of us have this expertise and use histotechniques in our research.

In addition to using histology to study reproduction and development, 
researchers use it in taxonomy and systematics, physiology, biomarkers, 
toxicology, and molecular biology studies (of particular value is laser-capture 
microdissection to obtain targeted cells from FFPE or frozen sections to 
extract DNA and learn about the genetics of abnormal cells (tumors), 
microorganisms, or parasites.  A recent development in conservation is 
conservation medicine. Scientists and veterinarians are studying how diseases 
and anthropogenic changes in the environment are affecting biodiversity and 
habitats around the world. This requires use of histology to help diagnose 
diseases and identify etiologic agents, with the hope of managing conservation 
programs to improve the organisms' and humans' health ("one health").

In the Bay area, check out the University of California at Davis' School of 
Veterinary Medicine. They have a histology facility. Let me know if you need a 
contact there (or maybe someone from it will reply to Histonet!).

Esther C. Peters, Ph.D.
Assistant Professor
Department of Environmental Science & Policy
Biology Program/Medical Technology Coordinator
George Mason University
4400 University Drive, MSN 5F2
Fairfax, VA 22030-
Office: David King Hall 3057
Phone: 703-993-3462
Fax: 703-993-1066
epete...@gmu.edu

- Original Message -
From: Rene J Buesa 
Date: Sunday, February 26, 2012 5:09 pm
Subject: Re: [Histonet] Scope of Practice

> As you point out, histology is a fundamental tool in human AND 
> veterinary pathology and every clinical AND veterinary laboratory 
> performs histology procedures/tests routinely.
> In other fields of biology either animal or plant biology it is 
> NOT customary to do histology studies of plants or animals UNLESS 
> the researcher wants to study a specific aspect of the biology of 
> the subject s/he is studying.
> In this sense it is frequent to study reproduction histology or 
> whole histology of small animals or developmental steps (ontogeny).
> Other than that it is NOT a given that "natural studies/biology" 
> include histology work, and they are the exception, not the rule.
> Outside human or veterinary pathology, histology work is not frequent.
> René J.
> 
> --- On Sun, 2/26/12, Bharti Parihar  wrote:
> 
> 
> From: Bharti Parihar 
> Subject: [Histonet] Scope of Practice
> To: histonet@lists.utsouthwestern.edu
> Date: Sunday, February 26, 2012, 4:52 PM
> 
> 
> Hello everyone! I am currently enrolled in an HT program through 
> IUPUI and
> am starting to send resumes out  as I encroach into the end of the 
> program.I asked my supervisor recently if there was a scope for 
> this field in the
> world of conservation?! She wasn't sure but recommended this site 
> to me to
> try to find any answers. It seems as though while 
> biologists/zoologistsetc. are out there on the field studying the 
> respective life form they do,
> there would be a need for histology in there somewhere, but I 
> don't really
> know how that works in that realm. I'm only familiar with Clinical 
> Labssince that's all I've ever worked in. Any thoughts/ direction? 
> I'd like to
> get involved in that if possible. I'm looking for work in Calfornia,
> specifically the bay area if possible. But as long as I can take 
> the BART
> to where it is that's fine with me also. I wanna make driving to 
> work the
> last resort, but ya know, gotta work and pay the bills so, if I 
> have to
> drive, so be it. Thanks ahead of time to those that can shed light 
> on this
> subject matter for me!!!
> Sincerely,
>        Bharti Parihar
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[Histonet] Senior Research Assistant Position in Histology

2011-11-20 Thread Esther C Peters
Please see the following job announcement for a Senior Research Assistant at 
George Washington University in Washington, DC.

Contact Dr. Patricia Latham at GWU if you are interested in this position: 
plat...@mfa.gwu.edu

Full-time Research Assistant - Histotechnologist
A position is available for a histotechnologist in a new research core 
laboratory in the GWU School of Biomedical Sciences. This person will be 
expected to maintain a histology laboratory, including ordering of supplies, 
washing glassware and maintaining equipment for optimal function, daily logs 
with inventory of specimens and blocks, labeling of samples and slides, tissue 
processing and embedding, microtome and cryostat sections, routine stains, 
special stains and immunostains with appropriate controls, as required to meet 
the needs of researchers at GWU. This person will need to work independently to 
deliver excellent quality results in a timely manner. The person should have 
strong communication skills and managerial skills, since there will be a need 
to work with researchers in several labs and to maintain inventory from several 
sources, to keep track of the flow of specimens and charges. The position will 
require data entry into an audit-trail database and the mainten
ance of meticulous records, with an exchange of data to the research center 
off-site and to labs at international sites. This person should have some 
experience in laboratory research, implementation of new techniques and the 
ability to trouble-shoot problems that might arise in this setting. Ideally, 
the person will have an entreprenurial spirit, since the success of the lab 
will determine its future existence. The full-time position is assured for 2 
years, but it can be extended and/ or grow to full-time, if the lab is 
successful.

Supervision:
The work will be supervised by a Pathologist as Project Manager. 

Entry level qualifications:
•   Bachelor’s degree in a clinical science with a course in Histology or 
equivalent combination of training and experience.
•   Experience working in a research setting.
•   Favored is eligibility or certification as a Histotechnologist or 
Histotechnician by the American Society for Clinical Pathology.


Esther C. Peters, Ph.D.
Assistant Professor
Department of Environmental Science & Policy
Biology Program/Medical Technology Coordinator
George Mason University
4400 University Drive, MSN 5F2
Fairfax, VA 22030-
Office: David King Hall 3057
Phone: 703-993-3462
Fax: 703-993-1066
epete...@gmu.edu

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Re: [Histonet] blades

2011-06-24 Thread Esther C Peters
We put ours in a small slide box (plastic or styrofoam, 5-25 slides) that is 
clearly marked "Microtome Blades for Facing Blocks" to be used another day.

Esther C. Peters, Ph.D.
Assistant Professor
Department of Environmental Science & Policy
Biology Program/Medical Technology Coordinator
George Mason University
4400 University Drive, MSN 5F2
Fairfax, VA 22030-
Office: David King Hall 3057
Phone: 703-993-3462
Fax: 703-993-1066
epete...@gmu.edu

- Original Message -
From: "Webb, Dorothy L" 
Date: Friday, June 24, 2011 4:53 pm
Subject: [Histonet] blades

> Trying to clean up some things hanging out there in our lab and 
> wondering what everyone does with a blade that has been used 
> minimally and tech done for the day with the microtome.  Where do 
> you store that blade for use tomorrow or do you toss and not worry 
> about the cost involved?  I do not like them sitting on top of the 
> microtome.  Any good ideas??  Thanks, as always!
> 
> 
> 
>  
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