[Histonet] in situ for mRNA - refresher course?

2011-08-29 Thread Louise Renton
Hi all,

after more than a decade away from the bench  I  have been asked to start
doing ISH on cryosections for BMPs and TGFbetas (mRNA) . I desperately need
some guidance - even an offer to training me.  i don't even know waht type
of probes have been developed in the interim.  I am sure I can get some
funding for a couple of days overseas..

Of course, vendors with local representation  are welcome to contact me.  I
look forward to a HUMUNGOUS response

regards
-- 
Louise Renton
Bone Research Unit
University of the Witwatersrand
Johannesburg
South Africa
+27 11 717 2298 (tel  fax)
073 5574456 (emergencies only)
There are nights when the wolves are silent and only the moon howls.
George Carlin
No trees were killed in the sending of this message.
However, many electrons were terribly inconvenienced.
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[Histonet] placental tissue

2011-08-29 Thread An Eerdekens
Dear collegues,

I want to fixate placental tissue. What is the best solution to use? 
Formaldehyde 4%? neutral-buffered 10% formal saline? Other?
Are there some tips and tricks while working with placental tissue?

Thanks for your help.

Regards

Dr An Eerdekens
University Hospitals Leuven
Belgium
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RE: [Histonet] peggy wenk comments on HT/HTL practical

2011-08-29 Thread joelle weaver


I was required to know and understand all this as well. I often have had to 
perform various aspects on an interview, and had no problems with this.
Joelle

Joelle Weaver MAOM, BA, (HTL) ASCP
 

From: b-freder...@northwestern.edu
To: lpw...@sbcglobal.net; mad...@verizon.net; histonet@lists.utsouthwestern.edu
Date: Mon, 29 Aug 2011 12:35:50 +
Subject: RE: [Histonet] peggy wenk comments on HT/HTL practical
CC: 

I remember having to know, regarding Peggy's comment on why a reagent was on a 
piece of tissue, for my HTL what was going in every step of the retic 
(oxidation,reduction,toning etc) and believe me it was on the exam. We were 
taught to know the why from the techs that trained us and had taken the exam. 
If you chose to ignore what they said, it was on your head.
 
As to the microtomy during an interview, I'm all for it as I have done it in 
the past (as an interviewer and interviewee)  and most recently, as we had a 
tech come in from Romania and how were we to know what she knew? Their program 
is a CLS degree and she chose histo from that. Great tech by the way- histo is 
not much different the world over, from what I can see.
 
Bernice
 
Bernice Frederick HTL (ASCP)
Senior Research Tech
Pathology Core Facility
ECOGPCO-RL
Robert. H. Lurie Cancer Center
Northwestern University
710 N Fairbanks Court
Olson 8-421
Chicago,IL 60611
312-503-3723
b-freder...@northwestern.edu
 
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Lee  Peggy Wenk
Sent: Sunday, August 28, 2011 6:41 PM
To: mad...@verizon.net; histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] peggy wenk comments on HT/HTL practical
 
Now add in a few other things, that I didn't directly mention in the original 
2006 HistoNet reply.
 
How many people are now using:
- automated HE stainers
- automated special stainers, including IHC stainer
- automated coverslippers
- automated microtomes
- disposable blades
 
Can you see why nearly everyone passed the practical? If they could cut a 
half-way decent section (with better microtomes and blades, easier to do), just 
put the slide on a machine and let the machine stain it. To fail, they 
basically had to NOT follow a LOT of directions, such as submitting colon for 
small intestine, submitting autolyzed gall bladder, doing the wrong stain (like 
doing a Prussian blue for iron, instead of the requested colloidal iron), 
grossing the tissue too small, microtoming too thick, putting the institution's 
name on the label, etc. Automation makes it easier to produce better sections 
and better stains, particularly if someone is a mediocre tech to begin with.
 
As to whether the person understands the theory when using automated stainers - 
well, the fact that many of the people submitting the practical could pass the 
practical but would fail the written - that has been going on since ancient 
times, when staining was done by hand. They could follow the directions, but 
didn't know the reasons. Pour on solution A for 5 minutes, pour it off, pour on 
solution B for 10 minutes, rinse it off, and it's done. 
No idea what is in solution A or B, or what chemicals are binding to what 
components in the tissue, etc. Whether someone is doing the stain by hand or by 
machine, it's up to the person to have the curiosity to find out what is going 
on. Some people don't have it, and don't feel the urge to learn.
 
That's one of the reasons I like going to state and national meetings, and 
reading HistoNet. These people WANT to learn! Hurrah for them! And there are a 
lot of people in the histology community willing to help people who WANT to 
learn - answering HistoNet, giving talks at state and national meetings, being 
a mentor, etc. Hurrah for them too!
 
Peggy A. Wenk, HTL(ASCP)SLS
Beaumont Health Systems
Royal Oak, MI 48073
 
The above are my opinions and not those of my institution.
 
-Original Message-
From: mad...@verizon.net
Sent: Sunday, August 28, 2011 2:23 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] peggy wenk comments on HT/HTL practical
 
 
The  dropping of the practical was explained so well by Peggy Wenk. I
   never  got  into  the  debate(glad  I  did  not  after  reading Peggys
   comments),  I  would  have argued to keep it.  That said, indeed it is
   outdated.  The  fact  that  we  were  the last to do it I guess speaks
   volumes.  I did struggle getting tissues for it for sure.  Modern day,
   modern  thinking.  Thanks  for the information Peggy and of course all
   you do fo this field.
 
   Nick(Rocky) Madary, HT/HTL(ASCP)QIHC
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RE: [Histonet] Returning to Histology-Another Idea Won't Work

2011-08-29 Thread joelle weaver

With all due respect and regard that should be afforded to the indisputable 
value of experience ( in time spans of 10 years or more), I would add that I do 
not see how this could be exchanged for  academics.To me they are different 
animals- both adding something to the knowledge base of the person ( and 
speaking from my perspective of having both under my belt),  and from my 
experience they are beneficial and useful to me, though in very different ways 
and different situations. I do not have the routes in front of me, and don't 
spend the time reviewing them that I formerly did, since I am not teaching at 
the moment, but I do not recall any experience level for any route stipulating 
10 years? 

Joelle Weaver MAOM, BA, (HTL) ASCP
 

 From: histot...@imagesbyhopper.com
 Date: Sat, 27 Aug 2011 20:06:18 -0400
 To: lpw...@sbcglobal.net
 Subject: Re: [Histonet] Returning to Histology-Another Idea Won't Work
 CC: histonet@lists.utsouthwestern.edu; araniqks...@yahoo.com
 
 10 years experience to qualify for taking the exam? Is that an ASCP 
 requirement? It sounds like they might be exchanging experience for the 
 bachelor's degree? Have you checked out the online courses? I believe there 
 are some that offer the bachelor's degree.
 
 Michelle
 
 Sent from my iPhone
 
 On Aug 27, 2011, at 1:45 PM, Lee  Peggy Wenk lpw...@sbcglobal.net wrote:
 
  It looks like the time limits prohibit me from trying this, since I did it 
  so long ago
  
  What is IT? What is prohibiting you from taking the HTL exam? What does 
  having taken and passed the HT exam have to do with taking the HTL exam?
  
  Sorry, I'm really lost as to what you need, and how to help you.
  
  Peggy A. Wenk, HTL(ASCP)SLS
  Beaumont Hospital
  Royal Oak, MI 48073
  
  The above response reflects my opinion, and not the hospital's view.
  
  -Original Message- From: Paula
  Sent: Thursday, August 25, 2011 3:31 PM
  To: histonet@lists.utsouthwestern.edu
  Subject: [Histonet] Returning to Histology-Another Idea Won't Work
  
  I thought it might be good to study and try for the HTL (already have 
  school for HT and am certified) but it looks like the time limits prohibit 
  me from trying this, since I did it so long ago. Anyone else have any 
  ideas? I'd gladly buy the books and study. Cannot get into a lab here in NC 
  without current experience. The closest school is in western NC, about 5 
  hours away. I didn't see anything near me in Raleigh. I was going to 
  purchase the textbooks but now I see this won't work either:
  
  Histotechnologist, HTL(ASCP)
  
  Application Fee: $210
  
  To be eligible for this examination category, an applicant must
  satisfy the requirements of at least one of the following routes:
  
  Route 1: Baccalaureate degree from a regionally
  accredited college/university with a combination of 30 semester hours
  (45 quarter hours) of biology and chemistry AND successful completion of
  a NAACLS accredited Histotechnician or Histotechnology program within
  the last 5 years; OR
  
  Route 2: Baccalaureate degree from a regionally
  accredited college/university with a combination of 30 semester hours
  (45 quarter hours) of biology and chemistry AND one year full time
  acceptable experience in a histopathology (clinical, veterinary,
  industry or research) laboratory in the U.S., Canada or an accredited
  laboratory* within the last ten years.
  
  *laboratory accredited by a CMS approved accreditation organization (i.e., 
  AABB, CAP, COLA, DNV, The Joint Commission, etc.)
  
  Clinical Laboratory Experience
  
  To fulfill the experience requirement for the Histotechnologist
  examination, you must have experience, within the last ten years, in the
  following areas:
  
  Fixation
  Microtomy
  Processing
  Staining Any ideas? I have posted this before, but I keep on trying!
  
  Paula
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RE: [Histonet] harrasment for humble histotechs

2011-08-29 Thread joelle weaver

I think that I have worked with some of these people, like I posted previously, 
if you don't commit the effort to learn and perfect your technique and 
understanding when you are learning and a student, and try to do a work 
around- short cut,  by cheating, IT WILL SHOW at some point. This may not 
catch up with you that day, or even the next, but in a specific lab or market, 
people get to know pretty quickly and easily who is really committed to doing 
quality work , who knows the how and why of what they are doing, and who just 
shows up for a job...

Joelle Weaver MAOM, BA, (HTL) ASCP
 

 From: histot...@imagesbyhopper.com
 Date: Sat, 27 Aug 2011 16:50:26 -0400
 To: mad...@verizon.net
 Subject: Re: [Histonet] harrasment for humble histotechs
 CC: histonet@lists.utsouthwestern.edu
 
 :o). I'm not even sure I could find my results after all these years and 9 
 moves!
 
 I *do* remember how picture perfect those slides had to be though. Tiny air 
 bubble=graded down. Folds=forget it. Knife marks=bad.
 
 I did both the HT and the HTL practicals and now new students don't even have 
 to submit them. I didn't cheat, but over the years I saw students attempting 
 to cheat. If I saw them, I would remind them that they were to work 
 independently, but who knows what they did when I wasn't looking?
 
 Integrity is what you do when no one is looking.
 
 
 
 Sent from my iPhone
 
 On Aug 27, 2011, at 3:25 PM, mad...@verizon.net wrote:
 
  
  Gentle harrassment. I encourage you to look at you scores for your
  practical and written exam. Between gigs I am getting my important
  documents together and found my old scores for the HTL, no thte HT,
  however, both parts of the exam were taken by yours truly. Never got
  into the talk of practical vs no practical. I do think it si a good
  idea to keep it. Honest techs will be proud to do a practical. Looking
  at scores made me feel good that the next great job is right around
  the corner.
  
  Nick(Rocky) Madary, HT/HTL(ASCP)QIHC
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[Histonet] Moh's Tech Opening in Cleveland

2011-08-29 Thread Brian- Prometheus
We are currently looking for a Moh's Tech brand new graduate or with
experience. 

 

Position is with a large Dermatology Practice in Cleveland with 6 offices in
the Greater Cleveland Area. 

 

The position involves some travel between offices as well as working 1-2
days in their Dermatopathology lab. 3-4 days the candidate would be cutting
tissue for the same physician mostly. 

 

Please contact me today if you might know anyone interested!

 

Thanks!

 

 

 

Brian Feldman

Principal

Prometheus Healthcare 

Office 301-693-9057

Fax 301-368-2478

 
http://us.mc538.mail.yahoo.com/mc/compose?to=br...@prometheushealthcare.com
 br...@prometheushealthcare.com

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

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

  http://twitter.com/PrometheusBlog http://twitter.com/PrometheusBlog

 

 

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[Histonet] troubleshooting Oil Red O

2011-08-29 Thread Denise G Crowley
Hi all,

I'm using the Churukian method  posted by Gayle Callis a few years ago and I 
have encountered a strange problem.  The lipid stains fine, and the Gill's 
hematoxylin looks good before I coverslip with Vectashield Hard Set aqueous 
mounting medium.  But within a matter of minutes, the hematoxylin leaches out.  
I popped off the coverslip and tried again with Mayer's hematoxylin with the 
same results.  I have used Vectashield Hard Set before, in fact I pulled a 5 
year old control that still looks great.  Does anyone have any ideas? 

Denise Crowley
Histology Facility Manager
Koch Center for Integrative Cancer Research
Massachusetts Institute of Technology
500 Main St. 76-182
Cambridge MA 02139
617-258-8183
dencr...@mit.edu


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[Histonet] excellent condition used embedding center

2011-08-29 Thread Pathology Lab
Im looking for an excellent conditions embbeding center 

 
Lcda. Mary V. Guerrero,BS, MBA,HtL              
Administradora/Coordinadora General
 Pathology Lab.
55 N. Dr. Basora Edificio Médico IV Oficina 206
Mayaguez, Puerto Rico 00680
Tel. 787-834-8202  Fax: 787-831-5255

    

Sra. Dimary Valentín
Secretaria Area de Facturación


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ALGUNA SOBRE EL CONTENIDO DE ESTA TRANSMISION ELECTRONICA.  
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Re: [Histonet] troubleshooting Oil Red O

2011-08-29 Thread Geoff McAuliffe
It may be that Vector has changed the formulation for Hard Set. I 
suggest you call them up. I have found their technical support to be 
excellent.


Geoff

On 8/29/2011 10:30 AM, Denise G Crowley wrote:

Hi all,

I'm using the Churukian method  posted by Gayle Callis a few years ago and I 
have encountered a strange problem.  The lipid stains fine, and the Gill's 
hematoxylin looks good before I coverslip with Vectashield Hard Set aqueous 
mounting medium.  But within a matter of minutes, the hematoxylin leaches out.  
I popped off the coverslip and tried again with Mayer's hematoxylin with the 
same results.  I have used Vectashield Hard Set before, in fact I pulled a 5 
year old control that still looks great.  Does anyone have any ideas?

Denise Crowley
Histology Facility Manager
Koch Center for Integrative Cancer Research
Massachusetts Institute of Technology
500 Main St. 76-182
Cambridge MA 02139
617-258-8183
dencr...@mit.edu


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Neuroscience and Cell Biology
Robert Wood Johnson Medical School
675 Hoes Lane, Piscataway, NJ 08854
voice: (732)-235-4583
mcaul...@umdnj.edu
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[Histonet] iliac artery attachment to slides?

2011-08-29 Thread Herrick, James L. (Jim)
Good morning everybody!!

I am trying to attach iliac arteries embedded in MMA (methyl
methacrylate + dibutyl phthalate + perkadox 16) to gelatin coated slides
to allow us to stain them with the Movat's Pentachrome. Unfortunately, I
have a real problem getting them to attach - shortly after they are
placed into 2-MEA for plastic removal, the section detaches from the
slide.

I have mounted hundreds of sections to slides before with great success,
but have never tried iliac arteries before. When mounting them using the
conventional method (a drop of 50% ETOH, roll them onto the slide using
a plastic coverslip, clamping the stack and placing it into a 45 - 50
degree Celcius oven for 24 to 48 hours), the sections attach beautifully
and do not fall off during deplasticization. The problem is that they
are completely consumed with wrinkles around the entire circular area of
the artery, rendering them unuseable.

I have tried dry mounting (without using 50% ETOH or dH2O), I have tried
floating the section onto a slide from a warm ETOH or dH2O solution (in
water bath), I have tried using a slide warmer, I have tried a heat gun
at low and high temperature settings, etc., etc.. The sections look
great using the dry mounting methods (i.e. they don't wrinkle), but they
detach from the slide very quickly following submersion in 2-MEA. It
appears to me that the wrinkles appear following the introduction of the
ETOH or dH2O.

If anyone would have any suggestions or comments, it would be greatly
appreciated. Thanks again for all of your help.

Have a great day!!
Jim

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[Histonet] lot to lot

2011-08-29 Thread Mary Helie

Good Afternoon

I would like to get an idea of how many slides people are running for 
lot to lot antibody and detection testing. For example would a tonsil 
with good internal negative and positive elements be good enough to 
validate a new lot of LCA?


Thank you
Mary

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Re: [Histonet] lot to lot

2011-08-29 Thread Rene J Buesa
I think yes!
René J.

--- On Mon, 8/29/11, Mary Helie mary.he...@yale.edu wrote:


From: Mary Helie mary.he...@yale.edu
Subject: [Histonet] lot to lot
To: histonet@lists.utsouthwestern.edu
Date: Monday, August 29, 2011, 12:06 PM


Good Afternoon

I would like to get an idea of how many slides people are running for lot to 
lot antibody and detection testing. For example would a tonsil with good 
internal negative and positive elements be good enough to validate a new lot of 
LCA?

Thank you
Mary

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Re: [Histonet] lot to lot

2011-08-29 Thread Patti Loykasek
I know different people do lot to lot checks in various ways. We use 
concentrated antibodies, and so we like to do a 'sandwich' titer check on the 
new lot using our usual tissue control tissue. For example, if the last CD20 
lot was at 1:100 we would check the new lot at 1:50, 1:100, 1:200 using tonsil 
tissues  our standard SOPs. I did have 1 inspector tell me they thought that 
was unnecessary. It's our preference to do 3 titers  assess the maximum 
performance in one fell swoop. Our detection lot to lot check is completely 
different. We check 8-10 different antibodies using our standard control tissue 
with the new detection lot. we use antibodies with a variety of cellular 
expressions to assess cytoplasmic, membranous  nuclear expression. We make 
sure to include some of our 'fussy' antibodies. Of course we have SOPs  forms 
to go along with this. 
Call me crazy - I prefer to think of it as meticulous  dedicated! We have had 
a couple of problems with detections over the years. 
Just my 2 cents. 

Patti Ann Loykasek HTL, QIHC
PhenoPath Laboratories


On Aug 29, 2011, at 9:06 AM, Mary Helie wrote:

 Good Afternoon
 
 I would like to get an idea of how many slides people are running for lot to 
 lot antibody and detection testing. For example would a tonsil with good 
 internal negative and positive elements be good enough to validate a new lot 
 of LCA?
 
 Thank you
 Mary
 
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[Histonet] Histotech position

2011-08-29 Thread Bilger, Andrea
Histonet members,

York Hospital in York Pennsylvania is looking for a histotech to work day shift 
Monday through Friday with an occasional 5 hours on Saturday.  If you are 
interested, apply at www.wellspan.orghttp://www.wellspan.org or contact:

Andrea Bilger
Team Leader, Histology
York Hospital
1001 South George St.
York, Pa. 17405
717-851-5040

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[Histonet] Thanks!

2011-08-29 Thread Mary Helie

Thank you all- this was very helpful. I appreciate it.

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[Histonet] Cost of an HE

2011-08-29 Thread Carol Fields
Hi Netters,

If anyone has figured the cost of an HE lately will you pleas share the
info with me?  It has been awhile since I have done this.  My email is
below if you do not mind sharing.
Thank you in advance.
Carole

Carole Fields, HT (ASCP)
Histology Supervisor
Northside Hospital
Atlanta, GA 30342
carol.fie...@northside.com




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[Histonet] Re: iliac artery attachment to slides?

2011-08-29 Thread Johnson, Teri
Hi Jim, sounds like you are having a time of it.

I figure Jack Ratliff will chime in as soon as he sees this. In the meantime I 
will give you the same advice he gave to me.

If you are having troubles with tissues adhering, try Haupt's adhesive. You can 
find recipes on the internet to make it yourself, or you can buy it 
commercially ready to use (www.dornandhart.com). I have heard from several 
people who use this consistently with their MMA and they swear by it. Have you 
tried stretching the sections using a few drops of 50% alcohol and a couple of 
soft brushes prior to covering in plastic and clamping? It's going to be tough 
getting circular tissues wrinkle free. I hope others with more experience than 
me will chime in on this.

Best wishes,

Teri Johnson, HT(ASCP)QIHC
Head, Histology and Electron Microscopy
Stowers Institute for Medical Research
Kansas City, MO


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Re: [Histonet] Cost of an HE

2011-08-29 Thread Rene J Buesa
The information on direct costs is in separate e-mail
René J.

--- On Mon, 8/29/11, Carol Fields carol.fie...@northside.com wrote:


From: Carol Fields carol.fie...@northside.com
Subject: [Histonet] Cost of an HE
To: histonet@lists.utsouthwestern.edu
Date: Monday, August 29, 2011, 2:04 PM


Hi Netters,

If anyone has figured the cost of an HE lately will you pleas share the
info with me?  It has been awhile since I have done this.  My email is
below if you do not mind sharing.
Thank you in advance.
Carole

Carole Fields, HT (ASCP)
Histology Supervisor
Northside Hospital
Atlanta, GA 30342
carol.fie...@northside.com




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[Histonet] Charcoal filters for VIP1000 K series

2011-08-29 Thread gayle callis
There are two charcoal filters (#6160) available for a Sakura Finetek VIP
1000, K series tissue processor. These are free for the lab  who can use
them.  Contact Maria Jerome [mjerome.mt...@gmail.com] for shipping
arrangements.   She is not on Histonet.  

 

 

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Re: [Histonet] training techs

2011-08-29 Thread histot...@imagesbyhopper.com
Way to go Patsy!! :o)

Sent from my iPhone

On Aug 29, 2011, at 5:36 PM, Patsy Ruegg pru...@ihctech.net wrote:

 Hey Everyone,
 
 
 
 The third tech I trained in the last 3 years just passed her HTL exam last
 Friday, that all makes me feel pretty good.  I just signed an affiliate
 agreement to be a clinical training site for the Histology program at UND
 today, they are sending me another student who will be with me for 2
 semesters.  
 
 
 
 Regards,
 
 Patsy
 
 
 
 Patsy Ruegg, HT(ASCP)QIHC
 IHCtech, LLC
 Fitzsimmons BioScience Park
 12635 Montview Blvd. Suite 215
 Aurora, CO 80010
 P-720-859-4060
 F-720-859-4110
 wk email  mailto:pru...@ihctech.net pru...@ihctech.net
 web site  http://www.ihctech.net www.ihctech.net
 
 
 
 
 This email is confidential and intended solely for the use of the Person(s)
 ('the intended recipient') to whom it was addressed. Any views or opinions
 presented are solely those of the author. It may contain information that is
 privileged  confidential within the meaning of applicable law. Accordingly
 any dissemination, distribution, copying, or other use of this message, or
 any of its contents, by any person other than the intended recipient may
 constitute a breach of civil or criminal law and is strictly prohibited. If
 you are NOT the intended recipient please contact the sender and dispose of
 this e-mail as soon as possible.
 
 
 
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Re: [Histonet] peggy wenk comments on HT/HTL practical

2011-08-29 Thread histot...@imagesbyhopper.com
Interestingly, I have never been required to section tissue in a job interview. 
I have worked at four hospitals, three private labs and one research facility 
(hubby moved us around a bit!)

I just recently hired two techs, directly out of school with no real world 
experience. I did ask them to cut some slides for me!  ;o)

Michelle

Sent from my iPhone

On Aug 29, 2011, at 9:05 AM, joelle weaver joellewea...@hotmail.com wrote:

 
 
 I was required to know and understand all this as well. I often have had to 
 perform various aspects on an interview, and had no problems with this.
 Joelle
 
 Joelle Weaver MAOM, BA, (HTL) ASCP
 
 
 From: b-freder...@northwestern.edu
 To: lpw...@sbcglobal.net; mad...@verizon.net; 
 histonet@lists.utsouthwestern.edu
 Date: Mon, 29 Aug 2011 12:35:50 +
 Subject: RE: [Histonet] peggy wenk comments on HT/HTL practical
 CC: 
 
 I remember having to know, regarding Peggy's comment on why a reagent was on 
 a piece of tissue, for my HTL what was going in every step of the retic 
 (oxidation,reduction,toning etc) and believe me it was on the exam. We were 
 taught to know the why from the techs that trained us and had taken the exam. 
 If you chose to ignore what they said, it was on your head.
 
 As to the microtomy during an interview, I'm all for it as I have done it in 
 the past (as an interviewer and interviewee)  and most recently, as we had a 
 tech come in from Romania and how were we to know what she knew? Their 
 program is a CLS degree and she chose histo from that. Great tech by the way- 
 histo is not much different the world over, from what I can see.
 
 Bernice
 
 Bernice Frederick HTL (ASCP)
 Senior Research Tech
 Pathology Core Facility
 ECOGPCO-RL
 Robert. H. Lurie Cancer Center
 Northwestern University
 710 N Fairbanks Court
 Olson 8-421
 Chicago,IL 60611
 312-503-3723
 b-freder...@northwestern.edu
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Lee  Peggy 
 Wenk
 Sent: Sunday, August 28, 2011 6:41 PM
 To: mad...@verizon.net; histonet@lists.utsouthwestern.edu
 Subject: Re: [Histonet] peggy wenk comments on HT/HTL practical
 
 Now add in a few other things, that I didn't directly mention in the original 
 2006 HistoNet reply.
 
 How many people are now using:
 - automated HE stainers
 - automated special stainers, including IHC stainer
 - automated coverslippers
 - automated microtomes
 - disposable blades
 
 Can you see why nearly everyone passed the practical? If they could cut a 
 half-way decent section (with better microtomes and blades, easier to do), 
 just put the slide on a machine and let the machine stain it. To fail, they 
 basically had to NOT follow a LOT of directions, such as submitting colon for 
 small intestine, submitting autolyzed gall bladder, doing the wrong stain 
 (like doing a Prussian blue for iron, instead of the requested colloidal 
 iron), grossing the tissue too small, microtoming too thick, putting the 
 institution's name on the label, etc. Automation makes it easier to produce 
 better sections and better stains, particularly if someone is a mediocre tech 
 to begin with.
 
 As to whether the person understands the theory when using automated stainers 
 - well, the fact that many of the people submitting the practical could pass 
 the practical but would fail the written - that has been going on since 
 ancient times, when staining was done by hand. They could follow the 
 directions, but didn't know the reasons. Pour on solution A for 5 minutes, 
 pour it off, pour on solution B for 10 minutes, rinse it off, and it's done. 
 No idea what is in solution A or B, or what chemicals are binding to what 
 components in the tissue, etc. Whether someone is doing the stain by hand or 
 by machine, it's up to the person to have the curiosity to find out what is 
 going on. Some people don't have it, and don't feel the urge to learn.
 
 That's one of the reasons I like going to state and national meetings, and 
 reading HistoNet. These people WANT to learn! Hurrah for them! And there are 
 a lot of people in the histology community willing to help people who WANT to 
 learn - answering HistoNet, giving talks at state and national meetings, 
 being a mentor, etc. Hurrah for them too!
 
 Peggy A. Wenk, HTL(ASCP)SLS
 Beaumont Health Systems
 Royal Oak, MI 48073
 
 The above are my opinions and not those of my institution.
 
 -Original Message-
 From: mad...@verizon.net
 Sent: Sunday, August 28, 2011 2:23 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] peggy wenk comments on HT/HTL practical
 
 
The  dropping of the practical was explained so well by Peggy Wenk. I
   never  got  into  the  debate(glad  I  did  not  after  reading Peggys
   comments),  I  would  have argued to keep it.  That said, indeed it is
   outdated.  The  fact  that  we  were  the last to do it I guess speaks
   volumes.  I did struggle getting 

[Histonet] RE: Going for the HTL

2011-08-29 Thread Jeff and Wanda Gray
To Paula:
Who wrote, thought it might be good to study and try for the HTL (already
have school for HT and am certified) but it looks like the time limits
prohibit me from trying this, since I did it so long ago. Anyone else have
any ideas? I'd gladly buy the books and study. Cannot get into a lab here in
NC without current experience. The closest school is in western NC, about 5
hours away. I didn't see anything near me in Raleigh. I was going to
purchase the textbooks but now I see this won't work either:
There is an internet program just down the road in Charleston for HTLs:
www.musc.edu/histoprogram Our program is NACCLS approved, has start dates in
April and Sept. You can also call the director, Karen Brinker Geils @ (843)
792-4013. Take a look, I'll bet you can do it! It took me over 10 years, but
I got my BS and passed my HTL just this year! Life got in my way for a
while, but I did it, and I know you can too!
Wanda Shotsberger Gray 
HT/HTL (ASCP), QIHC


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[Histonet] Re: peggy wenk comments on HT/HTL practical

2011-08-29 Thread Bob Richmond
I really appreciate Peggy Wenk's analysis of the practical examination
and why it had to be dropped. I never really understood the issue
before.

I must confess I always enjoyed helping the prospective examinee
obtain exactly the right tissue.

No, this endometrium is poorly preserved. We'll arrange with surgery
for a completely fresh specimen - I'll block it initially for the
diagnosis, then we'll fix it overnight and then block it exactly to
specifications. - Ick - this one's been curetted - we'll get another
one.

I'll block the margins of this colon resection specimen, then we'll
pin a portion of tissue onto paraffin and fix it flat overnight.

Next time I do an autopsy we'll get a lumbar spinal cord in the
intact dura. I'll open the dura dorsally and ventrally with iridectomy
scissors, then we'll hang it in neutral buffered formalin for two
days. Then I'll tie the dura and dependent nerves with a cotton
string. When you embed you'll remove the string, taking care that dura
and nerves remain in position. After that it's all yours. If it
doesn't work the first time, we've got three more levels in the jar.

OK, I'm a geek, I'm 72 years old, I got a right.

Bob Richmond
Samurai Pathologist
Knoxville TN

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