Re: [Histonet] QIHC

2013-03-04 Thread Lee Peggy Wenk
Just to let everyone know - the Michigan Society of Histotechnologists have 
put together a Study Guide/Workbook, geared to help those studying for the 
QIHC. It is a workbook, where you have to look up the information in books, 
and write it in the booklet. There are no answers provided (it's not a 
multiple choice question book, it's writing out definitions and how 
procedures work). This workbook is tries to cover all the areas on the exam, 
as listed on the ASCP BOC QIHC exam content outline. It is to help people 
get organized in their studying. $20.


For more information, go to the MSH webpage:
www.mihisto.org
Click on Education
Click on Study Guides

Print out the order form at the bottom.

Disclosure statement: I am a member of MSH. I do not receive any money from 
the sale of the QIHC Study Guide. Any money made (after printing and mailing 
costs) goes to support MSH.


Peggy A. Wenk, HTL(ASCP)SLS

-Original Message- 
From: Renee H. Workman

Sent: Friday, March 01, 2013 11:26 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] QIHC

I will be taking the QIHC soon has anyone taken it recently.  I lost my QIHC 
when I changed jobs and want to get


it back.


Renee H. Workman
W: 804-527-1316 | F: 804-270-0917
rhwork...@uro.commailto:rhwork...@uro.com | 
www.uro.comhttp://www.uro.com/






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Re: [Histonet] RESCUING UNDER DECALCIFIED BONE FROM PARAFFIN EMBEDDEDBLOCKS

2013-03-04 Thread Lee Peggy Wenk

Can you surface decal?

After facing the block on the microtome, getting a full face, pour some 
decalcification fluid in the lid of a coplin jar. Place the block faced side 
down in the decal solution, for about 30 minutes.


Rinse the acid off the block with some cool water (don't want acid dripping 
on the microtome blade holder and blade). Line the block up exactly on the 
microtome to the knife. The first 2-4 sections will be decalcified enough 
for you to cut. (That's why the block has to be lined up exactly - can't 
waste rough trimming off the 10-20 um of decalcified tissue.)


Peggy A. Wenk, HTL(ASCP)SLS
Beaumont Health System
Royal Oak, MI 48073

The opinions expressed are mine, and do not reflect on my place of 
employment.


-Original Message- 
From: Fiona J Morrow

Sent: Thursday, February 28, 2013 8:59 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] RESCUING UNDER DECALCIFIED BONE FROM PARAFFIN 
EMBEDDEDBLOCKS


Hi

Has anyone ever tried to reprocess bone tissue that has been under
decalcified and processed through to wax?

Thanks

Fi M


Fiona Morrow
Dept. of Infection and Immunity
KFloor, Room K118
Medical School
University of Sheffield
Beech Hill Road
Sheffield
S10 2RX

0114 271 2102
f.mor...@sheffield.ac.uk

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Re: [Histonet] Unencased Ameoba Stain

2013-03-04 Thread Lee Peggy Wenk

Getting back a little late (been out of state).

If this is Acanthamoeba, then we do a PASH and/or a GMS. These are cysts, 
and show up nicely with both. The cornea can be PAS positive also, so the 
Acanthamoeba are a darker pink against a lighter pink, while the GMS is 
gray/black against the green background. It looks a lot like pneumocystis 
with a GMS, but without the bull's eye, and about 2-3 times larger.


But it's the cyst wall that is staining with the PAS and the GMS, as the 
cyst has a lot of glycogen.


But you are asking for unencased amoeba. So that sounds like no cyst. Are 
you looking for just the trophozoites? I would suggest one of the Giemsa 
stains, or maybe a Brown and Hopps. A cresyl echt violet (actually cresyl 
violet acetate, but everyone still calls it by it's old name), would 
probably also work - I read about it in the NSH Journal of Histotechnology 
about 20 years ago for the trophozoites of pneumocystis, but I've never 
tried the stain.


Peggy A. Wenk, HTL(ASCP)SLS
Beaumont Health System
Royal Oak, MI 48073

The opinions expressed are mine, and do not represent BHS.

-Original Message- 
From: Joseph Brooks

Sent: Wednesday, February 27, 2013 11:12 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Unencased Ameoba Stain

Hello All,

One of our Neuropath docs is inquiring about a special stain for unencased
ameobas in cornea biopsies.  I did a search and Gridley's Method was the
best option that appreaded.  Is there someone that could either verify this
stain will work on this organism or let me know what you stain you are
using?  Thanks in advance.

Matt Brooks
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Re: Re: [Histonet] teeth sectioning

2013-03-04 Thread E. Wayne Johnson 朱稳森

Jack,
That sounds really awesome.

I did some work with the teeth of sows (female pigs) from
specimens collected at slaughter.  Those are very difficult to decalcify,
and when finished, are likely to have no nuclear detail remaining.

Interested to hear what you learn

Wayne Johnson
Beijing Enable Ag Consulting
Yuanmingyuan West Road Meiyuan Com,


On 3:59, Jack Ratliff wrote:

Mes,

This is a very good question and I look forward to answers from individuals 
that have accomplished this with PMMA and a rotary microtome with 
tungsten-carbide knives. If you are talking about an undecalcified specimen 
embedded in PMMA, then I would imagine that the age of the rat could affect the 
ability to achieve an adequate infiltration of the resin. Again, I look forward 
to what others have to say about their success by the method you have outlined.

On the other hand, I know you can achieve the micron thickness you desire if 
you were to use a non-contact femtosecond laser! The machine I am talking about 
is basically a laser microtome manufactured by Rowiak in Germany and it is 
officially called the TissueSurgeon. In fact, Dr. Heiko Richter from Germany 
has accomplished what you ask with human teeth, revealing the full anatomy of 
the tooth and even with ameloblasts on the enamel surface!

I would be interested to hear more about your project. I will be traveling to 
Germany one week from today to work with this laser microtome until the end of 
the month so I could arrange to have laser cut sections made for you if you are 
interested and unable to make your cuts using PMMA and a rotary microtome. If 
you would like more information, please feel free to contact me by email reply.

Best Regards,

Jack



Jack L Ratliff
Owner/Histologist, Ratliff Histology Consultants, LLC
Chairman, Hard Tissue Committee - National Society for Histotechnology



On Mar 1, 2013, at 7:03 PM, mesruh turkekulturke...@gmail.com  wrote:

   

Dear Histonetters,


I have one more question. Is it possible to obtain 5-10um thick sections of
PMMA embedded teeth using regular Leica paraffin microtome (RM2265)
equipped with disposable tungsten carbide blade?

Thanks,
Mes
On Fri, Mar 1, 2013 at 7:40 PM, mesruh turkekulturke...@gmail.com  wrote:

 

Dear Histonetters,


I am studying bone and teeth growth in rat maxilla. I will inject calcein
green and would like to fix, embed and sections the rat maxilla.
Any suggestions for the best method to fix, embed and section the samples
for fluorescnet microscopy?

Thank you very much!

Mes HTL (ASCP)
Memorial Sloan-Kettering Cancer Center

On Fri, Mar 1, 2013 at 1:01 PM,
histonet-requ...@lists.utsouthwestern.edu  wrote:

   

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When replying, please edit your Subject line so it is more specific
than Re: Contents of Histonet digest...


Today's Topics:

   1. FNA Clia Guidelines (PicheGrocki, Jessica)
   2. RE: FNA Clia Guidelines (Horn, Hazel V)
   3. GSH Symposium April 12-14 (Zimmerman, Billie)
   4. FSH abstracts deadline (Jerry Santiago, MSEd, HTL (ASCP) QIHC)
   5. (no subject) (Vikrant Piprode)
   6. The GSH 4oth Anniversary Meeting (David Kemler)
   7. QIHC (Renee H. Workman)


--

Message: 1
Date: Thu, 28 Feb 2013 20:26:30 +
From: PicheGrocki, Jessicajpiche-gro...@wtbyhosp.org
Subject: [Histonet] FNA Clia Guidelines
To: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Message-ID:

631955447a364b45b9458d2905635110655d2...@win08-mbx-01.wtbyhosp.org
Content-Type: text/plain; charset=s-ascii

Hi All,

Quick questionwhat are the Clia requirements for Fine needle
aspirate procedures? Is it considered high complexity testing? And who
prepares the slides when the needle is handed off?

Thank you,

Jessica Piche, HT(ASCP)



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Message: 2
Date: Thu, 28 

[Histonet] pH and temperature

2013-03-04 Thread Emily Sours
Hello!

Can someone explain why pH is temperature dependent?
Really, I'm just worried about pHing 4% paraformaldehyde at about 50
degrees Celsius.  If I wait until it cools down to room temp, the para
usually precipitates--I assume because the pH is off.
I know I could measure the pH at room temperature, but I'm not making para
anytime soon, and I just thought of this.
By the way, the pH we are aiming for is 7.2 to 7.4

Emily


By bitching and bitching and bitching, they could exhaust the drama of
their own horror stories. Grow bored. Only then could they accept a new
story for their lives. Move forward.

-Chuck Palahniuk, Haunted
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[Histonet] KY HT Poisitons

2013-03-04 Thread Hale, Meredith
Please no Recruiter calls

Great opportunity for Histotechnician's in Crestview Hills, KY ! Tri-State 
Gastroenterology Associates is  a multi-physician practice located in Northern 
Kentucky. Its mission is To provide compassionate, high quality, 
cost-effective care to pateints with gastrointestinal problems  Looking for 2 
Full Time HT/HTL's  ( 32 hours a week is full time employement at this practice 
)

* Meet CLIA Grossing Requirements : CFR  493.1489,  
http://wwwn.cdc.gov/clia/regs/toc.aspx/ ,prior experience grossing GI specimens

* Supervisor experience preferred

* HT/HTL ASCP Certified

* Experience with CLIA and CAP

* Experience writing  and maintaining policies and procedures

* Prior laboratory start up experience is preferred

* Ability to work independently
Duties include:

* Grossing

* Embedding

* Microtomy

* Staining; routine and special stains only

* Maintain supply orders and laboratory budget

* Ability to be flexible and take on additional duties' as needed

* Ability to work independently

* Maintenance of laboratory for inspections

* Maintenance of quality records


  Interested applicants should contact Meredith Hale; phone 214-596-2219 or 
through email mh...@miracals.commailto:mh...@miracals.com


Meredith Hale HT  (ASCP)cm
Director External Sales Support

Miraca Life Sciences
6655 North MacArthur Blvd.
Irving , Texas 75039
Office: 214-596-2219
Cell: 469-648-8253
Fax: 1-866-688-3280
mh...@miracals.commailto:mh...@miracals.commailto:mh...@miracals.com%3cmailto:mh...@miracals.com

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[Histonet] standards for embedding

2013-03-04 Thread Diana McCaig
I know this topic has been beaten to death in the past and do realize it is 
dependent on tissue
orientation, quantity of pieces in a block, and experience.

There are guidelines suggested by the College of Med Lab of Ontario in a 
document Oct 2008
that indicates the expected minimum daily range is

Specimens with no orientation   16-38 seconds per specimen
Specimens with orientation21 to 52 seconds peer 
specimen
Mixed cassettes  60-70 per hour

I would like to know if this is monitored and what do you if your techs are 
unable to reach these recommendations,
even after several years of experience.  I realize these are minimum 
suggestions and should be achievable but what
recommendations are suggested if a tech with over 10 years experience still 
averages close to 2 minutes a block.  On
average we may have 120-140 blocks a day and it takes 3.5-4 hours to embed.  I 
have had ergonomic assessments done.
They seem to maintain a constant level and will not strive for improvement.  
Any suggestions?

Diana
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Re: [Histonet] standards for embedding

2013-03-04 Thread Rene J Buesa
Ontario standards are above national and international averages and would be 
difficult to duplicate for the majority of labs.
Your averages are more in accordance with the averages I mention.
Please go to http://www.histosearch.com/rene.html to compare with the results 
of a survey I published.
René J.

From: Diana McCaig dmcc...@ckha.on.ca
To: 'histonet@lists.utsouthwestern.edu' histonet@lists.utsouthwestern.edu 
Sent: Monday, March 4, 2013 11:07 AM
Subject: [Histonet] standards for embedding

I know this topic has been beaten to death in the past and do realize it is 
dependent on tissue
orientation, quantity of pieces in a block, and experience.

There are guidelines suggested by the College of Med Lab of Ontario in a 
document Oct 2008
that indicates the expected minimum daily range is

Specimens with no orientation                      16-38 seconds per specimen
Specimens with orientation                            21 to 52 seconds peer 
specimen
Mixed cassettes                                              60-70 per hour

I would like to know if this is monitored and what do you if your techs are 
unable to reach these recommendations,
even after several years of experience.  I realize these are minimum 
suggestions and should be achievable but what
recommendations are suggested if a tech with over 10 years experience still 
averages close to 2 minutes a block.  On
average we may have 120-140 blocks a day and it takes 3.5-4 hours to embed.  I 
have had ergonomic assessments done.
They seem to maintain a constant level and will not strive for improvement.  
Any suggestions?

Diana
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[Histonet] RELIA Solutions HOT JOB ALERT and a link to my blog post Essential Tips for Working with a Recruiter 3/4/2013

2013-03-04 Thread Pam Barker
Hi Histonetters!!
I hope your week is off to a great start!!  I know mine is!!
I have a couple of new opportunities that I want to share.  Also I recently
started a blog called Dream Job Diva here is the link to one of my posts if
you think you might like to check it out.  This has been without a doubt my
most popular post which is why I chose it to share.  I have even had other
recruiting firms praise this post.  - Enjoy.
 Here is the link:
http://reliasolutionspambarker.wordpress.com/2012/07/28/esssential-tips-for-
working-with-a-recruiter/ 

Here are the hot jobs I want to share with you!
Histology Tech - East Texas - exciting opportunity to work in dermpath AND
work with one of the top Mohs techs in the country!
Histo Tech - Syracuse, NY - NYS license required
Histotechnician - East of Columbus, OH
IHC Specialist - Charlotte, NC
Grossing Histotech - Charlotte, NC

All of my clients offer excellent compensation, benefits and relocation
assistance.  These are full time permanent positions with stable secure
labs.  My clients are eager to interview and hire for these positions!
If any of these opportunities are the right one for you RELIA can make it
happen.

If you do take the time to read my blog post I would love feedback.
Thanks-Pam

Right Place, Right Time, Right Move with RELIA!

Thank You!
 Pam M. Barker
 
Pam Barker
President/Senior Recruiting Specialist-Histology
RELIA Solutions
Specialists in Allied Healthcare Recruiting
5703 Red Bug Lake Road #330
Winter Springs, FL 32708-4969
Phone: (407)657-2027
Cell: (407)353-5070
FAX: (407)678-2788
E-mail: rel...@earthlink.net 
www.facebook.com http://www.facebook.com/PamBarkerRELIA /PamBarkerRELIA
www.linkedin.com/in/reliasolutions
www.twitter.com/pamatrelia 





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[Histonet] Jekyll Island, GA

2013-03-04 Thread Zimmerman, Billie
Come to Jekyll Island for the sunrise, sunsets, and CEU's!! Earn up to 15 CEU's 
with incredible speakers and a chance to network with your peers for the low 
all inclusive rate of $135.  GSH is packing a punch for $135. GSH has planned 
an educational 40th anniversary celebration with fun, food, and time to visit 
the vendors.  We have filled our block of rooms, but the symposium rate has 
been extended and is still available at Oceanside Inns and Suites. Also,  if 
you love to ride bikes, bring them  to the beach.  I was impressed with the 
number of bike trails on the island.  Go to our website and join the 
celebration.  www.histosearch.com/gsh/http://www.histosearch.com/gsh/
If you have any questions or concerns please contact one of our officers.

Hope to see you there next month!

Wanda K. Simons
GSH President

WS/bz
Augusta State University and Georgia Health Sciences University have 
consolidated to become Georgia Regents University. Effective January 9, 2013, 
my email address has changed to bzimm...@gru.edu. Please update your address 
book to reflect this change.
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[Histonet] Re: teeth sectioning

2013-03-04 Thread Teri Johnson
This might or might not be helpful, but there was an article written by Janet 
Maas, Processing the Complete Canine Tooth. It is for paraffin sectioning.
JOH, Number 3, Sept 2002, pp. 137-140(4)

Teri Johnson, HT(ASCP)QIHC
GNF Histology Lab Manager
Genomics Institute of the Novartis Research Foundation
858-332-4752

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[Histonet] Re: pH and temperature

2013-03-04 Thread Emily Sours
Well, I found this on the site below:
To make an accurate pH measurement you need to use temperature
compensation. Exception is if you measure a pH of about 7.

Which makes me feel better.  Every other solution I pH is made at room
temperature.
I don't know why our para precipitates out--it might be because sometimes
the water doesn't reach a high enough temperature before it's added, or the
para solution cools down too much before the NaOH is added.  It hasn't done
it for a while though.

Emily


By bitching and bitching and bitching, they could exhaust the drama of
their own horror stories. Grow bored. Only then could they accept a new
story for their lives. Move forward.

-Chuck Palahniuk, Haunted


On Mon, Mar 4, 2013 at 1:28 PM, Tamara Howard thow...@unm.edu wrote:

  It is pretty basic chemistry...Even has a website!

 http://www.all-about-ph.com/ph-versus-temperature.html


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RE: [Histonet] Ventana HPV High/Low Replacements?

2013-03-04 Thread Michael Kent
Hi Jennifer,

I'd recommend looking at this study and comments on biomarkers in HPV:

The Lower Anogenital Squamous Terminology Standardization Project for 
HPV-Associated Lesions:
Background and Consensus Recommendations from the College of American 
Pathologists and the American Society for Colposcopy and Cervical Pathology

Arch Pathol Lab Med-Vol 136, October 2012 The CAP-ASCCP LAST Project--Darragh 
et al

Regards,

Mike

Michael Kent, MS, PhD
www.dermpathlab.com

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-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jennifer 
Masuzumi
Sent: Friday, March 01, 2013 2:09 PM
To: Histonet
Subject: [Histonet] Ventana HPV High/Low Replacements?

Hello everyone,

My lab is interested in starting HPV High and Low Risk ISH testing, but it 
seems like we just missed the boat on it. We have Benchmark XTs, but Ventana 
discontinued their HPV probes sometime around last December, and they don't 
have an alternative at this time. After talking with nearby labs that are 
currently using stockpiles of Ventana probes, they told me the following 
courses of action they were planning on using when their stock runs out:
-One lab is thinking of doing HPV by PCR -Another is thinking of switching to 
Dako probes

After discussing the possibility of Dako probes with Ventana and Dako, neither 
could recommend using them together because each side was unfamiliar with the 
other's reagents or system, though both said it might be possible.

Is anybody in a similar situation, looking for a replacement for the Ventana 
HPV High/Low Risk probes? Any insight on possibilities to pursue would be much 
appreciated!

Sincerely,
 
Jennifer Masuzumi
Sterling Pathology
Seal Beach, CA
jennifer.masuz...@sterlingpath.com
562-799-8900
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[Histonet] QC Slide retention

2013-03-04 Thread Riesen, Rebecca
How long do you folks retain you Daily QC slides?  Is it the same as the 
diagnostic slides?  I know the correct length of time for diagnostic slides 
in my particular area, but I wasn't sure if the same timeline applies to the 
actual daily HE or PAP QC slides. Is the retention of the actual 
documentation that I have of the quality of these stains each day sufficient? 
 I looked thru the archives, but could only find the previous discussions on 
Diagnostic slides.  Thanks Histonetters!!



Rebecca Riesen, Histology Supervisor, PRMC, Naples, FL
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[Histonet] Sponges and Processing

2013-03-04 Thread Laurie Colbert
If there is anyone out there that uses the blue sponges for biopsy specimens, 
would you please contact me offline?  I would like to know what your processing 
times are.  Thanks!

Laurie Colbert, HT (ASCP)
Histology Supervisor
PATH MD
8158 Beverly Blvd.
Los Angeles, CA  90048
(323) 648-3214 direct
(424) 245-7284 main lab

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[Histonet] RE: QC Slide retention

2013-03-04 Thread Bernice Frederick
We keep ours for 2 years- kind of like those lovely QC sheets for CAP.

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 Riesen, Rebecca
Sent: Monday, March 04, 2013 2:34 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] QC Slide retention

How long do you folks retain you Daily QC slides?  Is it the same as the 
diagnostic slides?  I know the correct length of time for diagnostic slides 
in my particular area, but I wasn't sure if the same timeline applies to the 
actual daily HE or PAP QC slides. Is the retention of the actual 
documentation that I have of the quality of these stains each day sufficient? 
 I looked thru the archives, but could only find the previous discussions on 
Diagnostic slides.  Thanks Histonetters!!



Rebecca Riesen, Histology Supervisor, PRMC, Naples, FL 
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[Histonet] RE: QC Slide retention

2013-03-04 Thread Weems, Joyce K.
We do the same.

Joyce Weems
Pathology Manager
678-843-7376 Phone
678-843-7831 Fax
joyce.we...@emoryhealthcare.org



www.saintjosephsatlanta.org
5665 Peachtree Dunwoody Road
Atlanta, GA 30342

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regarding the error in a separate email.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Bernice 
Frederick
Sent: Monday, March 04, 2013 3:46 PM
To: Riesen, Rebecca; histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: QC Slide retention

We keep ours for 2 years- kind of like those lovely QC sheets for CAP.

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 Riesen, Rebecca
Sent: Monday, March 04, 2013 2:34 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] QC Slide retention

How long do you folks retain you Daily QC slides?  Is it the same as the 
diagnostic slides?  I know the correct length of time for diagnostic slides 
in my particular area, but I wasn't sure if the same timeline applies to the 
actual daily HE or PAP QC slides. Is the retention of the actual 
documentation that I have of the quality of these stains each day sufficient? 
 I looked thru the archives, but could only find the previous discussions on 
Diagnostic slides.  Thanks Histonetters!!



Rebecca Riesen, Histology Supervisor, PRMC, Naples, FL 
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[Histonet] Per Diem opportunity near Port Chester, NY

2013-03-04 Thread Brannon Owens
Allied Search Partners is currently working with a large organization with
leading edge technologies to find a qualified Histology professional.

Location:  White Plains/Port Chester, NY area
Position title:  Histotechnician or Histotechnologist
Schedule:  Sunday 5am-1:30pm

Email bran...@alliesearchpartners.com for a full job description.  NY lab
license is required.

Brannon Owens
Recruitment Manager
Allied Search Partners


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[Histonet] RE: Antibody IDH1

2013-03-04 Thread Sue Hunter
We use Dianova's antibody at a 1:100 dilution on the Ultra.  CC1 cell 
conditioning for 40 minutes, antibody for 32 minutes - no heat.  We use 
Optiview detection system. No amp.  Make sure you are using the correct type of 
brain tissue for a control - most oligodendrogliomas should be positive, altho 
there are a few with other mutations.  Remember that this antibody only picks 
up the R132H point mutation.  This occurs in about 70% of oligos so it is 
possible that you happened to pick one that was positive for one of the other 
mutations.  Perhaps try a few different patient tissues.

Sue


Sue Hunter, Supervisor
Advanced Diagnostics
Beaumont Health System
Royal Oak MI
248-898-5146
shun...@beaumont.edu



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Zimmerman, 
Billie
Sent: Friday, February 22, 2013 4:21 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Antibody IDH1

Does anyone perform this antibody?? We can't get it to work on the Ventana 
Ultra.  PhenoPath in Seattle performs it on the Dako autostainer using a small 
size polymer detection kit.  I would appreciate any input.

Thanks,

Billie Zimmerman


Augusta State University and Georgia Health Sciences University have 
consolidated to become Georgia Regents University. Effective January 9, 2013, 
my email address has changed to bzimm...@gru.edu. Please update your address 
book to reflect this change.
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[Histonet] SOP numbering for whole lab

2013-03-04 Thread Cheryl
Help?  What kind of formula do you use when numbering and coding your SOPs for 
the lab?  Is there an easy way to keep them sorted and in line with all the 
regulatory bodies to help on inspection days?
 
Any suggestions welcome--we're starting from scratch.
 
Cheryl


 
 
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[Histonet] Back processing Histogel

2013-03-04 Thread Andrea Hooper
Has anyone back processed something that was both Histogel and FFPE embedded? 
If so, any hints or problems? 

Andrea
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[Histonet] Paraffin block archival storage

2013-03-04 Thread Clarence Owens
Does anyone know if there is a CAP or board of health regulation on storing 
archival paraffin blocks in a walk in morgue cooler. Currently we are storing 
our archival paraffin blocks in the morgue cooler for the ten year retention 
CAP regulation. The blocks are at a controlled temperature where the integrity 
of the blocks are not compromised. The blocks are stored in their block filing 
cabinet in one part of the cooler. Is there a problem with having the blocks 
stored in this area. Lastly the cooler is under lock and key and the key has to 
be signed out as well. This also provide a security aspect for the blocks and 
monitors who enters in and out of this secured area. Thanks for your help. 


Clarence Owens, HT (ASCP)
Lawrence General Hospital 
Lawrence, MA 01842
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