Re: [Histonet] RE: Paraffin Temperature Checks

2015-01-08 Thread b427297
I like to use a chart recorder on paraffin dispensers in case the thing goes 
whacko over a weekend and boils the paraffin, then goes back to normal before 
anyone notices.

Sent from my iPhone

 On Jan 8, 2015, at 6:10 PM, Elizabeth Chlipala l...@premierlab.com wrote:
 
 All of our logs are use logs so we record when we use any piece of equipment 
 and any QC or maintenance if required, we do not record or document anything 
 if we do not use it, other than lab temperature and humidity which we record 
 daily.
 
 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
 
 March 10, 2014 is Histotechnology Professionals Day
 
 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 Cooper, Brian
 Sent: Thursday, January 08, 2015 4:34 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Paraffin Temperature Checks
 
 For those of you out there that are fortunate enough to have tissue 
 processors or embedding centers that are used less often than daily-like 
 maybe even weekly (or even less frequently,) how often are you checking and 
 documenting the paraffin temperatures on said pieces of equipment?  For our 
 daily equipment, it's no big deal obviously.  But we have a research 
 processor and embedding center that doesn't get used often-sometimes for a 
 week or two, and if we're not touching the machine, it seems overkill to 
 document paraffin temps daily.
 
 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.edumailto:bcoo...@chla.usc.edu
 
 
 
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Re: [Histonet] Salary exempt/nonexempt status

2014-10-25 Thread b427297
Are you paid a. by the hour or was your pay quoted to you by b. yearly salary? 
C. Do you fill out a time card to record your hours?  If A and C are yes, you 
are non exempt. Your human resource department should have the answer. If you 
don't have an HR dept and you cant ask your boss to clarify, then you have a 
crummy relationship with your boss, and should look for a better job.

Sent from my iPhone

 On Oct 25, 2014, at 4:38 PM, Sebree Linda A lseb...@uwhealth.org wrote:
 
 I fought this very same battle having been salaried for many years and 
 gradually working more and more OT.  I worked solely with hourly employees 
 and was not a manager or supervisor.  Everyone I worked with accrued OT pay 
 but I did not and I was usually working the most OT.  I contacted our state 
 office of labor and workforce development and learned about the 
 exempt/nonexempt statuses.  Upon bringing this information to both my 
 institution's personnel department and eventually my manager, they reviewed 
 my position description along with several other employees.  They resolved 
 the issue by making me and some other people hourly with no cut in pay so now 
 I still work some overtime but accrue OT pay.  I also received back pay from 
 2 years of overtime.  
 
 Maybe CA has a labor department that could help you as well.
 
 Good luck,
 
 Linda A. Sebree
 
 From: histonet-boun...@lists.utsouthwestern.edu 
 [histonet-boun...@lists.utsouthwestern.edu] on behalf of GMail 
 [nguy0...@gmail.com]
 Sent: Saturday, October 25, 2014 3:16 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Salary exempt/nonexempt status
 
 Can someone please help me, I've been losing sleep over this ever since 
 moving to CA and working here.
 
 If you are paid a salary but NOT a supervisor or manager are you considered 
 exempt or nonexempt?
 
 I was told by someone that if you are salary but not in a managerial position 
 you are considered nonexempt and are entitled to earn OT.
 
 I have tried searching the laws in CA and the only thing I could find is: 1. 
 If you earn twice the wage of minimum wage you are exempt. 2.  If you are a 
 type of professional (doctors and lawyers etc) or in a managerial position 
 you are exempt
 
 With that being said, I believe a lot of people in the U.S with other 
 professions make twice the wage of #1, so does that mean they are all exempt?
 
 Please help me answer this question!
 
 Thank you in advance!
 
 Sent from my iPhone
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Re: [Histonet] Preventative Maintenance Fees Gone Wild

2014-08-29 Thread b427297
Pm or a service contract? 

Sent from my iPhone

 On Aug 29, 2014, at 11:58 AM, Sandra Cheasty cheas...@svm.vetmed.wisc.edu 
 wrote:
 
 Does anyone else think that  $8,266 sounds a bit high for a PM on a Lab 
 Vision Immunostainer? Does that price include a Happy Ending?
 
 
 
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Re: [Histonet] RE: Cornflaking artifact

2014-03-13 Thread b427297
Is this a tape coverslipper? If so, you do have minute traces of water 
carryover to your xylene. If there is even the hint of pink in you last 
dehydrant before xylene, you will get that cornflake artifact. Acetone wont 
help, because water still be present. Increase number of absolute alcohol 
before xylene, and check often for eosin carryover. This fixed our problem. 
Jackie O'

Sent from my iPhone

 On Mar 12, 2014, at 21:59, Sharon Scalise sscal...@beaumont.edu wrote:
 
 I am looking for help with cornflaking (tiny, brown dry spots under 
 coverslip)artifact.  We have been using fresh xylene on our stainer and 
 coverslipper, cleaned and wiped all containers dry before filling, tried 
 different lots of coverslipping film and had service on our coverslipper to 
 make sure it was functioning properly, including the xylene drip.  We 
 continue to have this artifact and it is driving us crazy.  It is sporadic 
 with no pattern of tissue type or placement on the slide.  Sometimes it lands 
 on tissue other times not.  Most of the time when we remove the coverslip and 
 re-coverslip it goes away (I am assuming because the acetone removes any 
 minute amounts of water that may be present).  We just cannot figure out 
 where the water is coming from.  Has anyone seen this artifact while using 
 the drying step on the prisma stainer?  We just recently started using the 
 drying on some slides and I am thinking maybe it is causing humidity???  I 
 cannot say for a fact that our cornflaking started at the same time, but it 
 is suspicious. HELP!
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Wait, Trevor 
 Jordan
 Sent: Wednesday, March 12, 2014 3:57 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Paraffin type and Tetracycline labelling Questions
 
 For those who have done Decalcified bone processing with paraffinwhat is 
 the best type of paraffin that you guys are familiar with?
 
 Also, if you are wanting to see a tetracycline label on the bone for bone 
 turnover, must undecalcified sections be used? How for a double tetracycline 
 label?
 
 
 Trevor Jordan Wait
 University of Texas Health Science Center, San Antonio Class of 2017 MD 
 Candidate Abilene Christian University Class of 2013 Graduate B.S.  
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Re: [Histonet] Soaking artifact

2014-01-05 Thread b427297
Your supervisor is wrong, and inexperienced.  What artifact?  Some tissues MUST 
be soaked on wet ice, spleen, liver, eye lens, anything bloody -   You just 
can't get quality sections without soaking some tissues. You can tell her I 
said so.  I'd like to know what artifact she is 'seeing'.
Jackie O'Connor



-Original Message-
From: Deanna Leslie dea.les...@gmail.com
To: histonet histonet@lists.utsouthwestern.edu
Sent: Sun, Jan 5, 2014 3:44 pm
Subject: [Histonet] Soaking artifact


Has anybody in histoland ever heard of this?  I have been cutting tissue
for 25 yrs and until recently I had never heard of this!
I am under contract to a facility and the supervisor there does not want
anybody to soak their tissue or use ice!  Your are supposed to use the cold
plate, because as I have stated soaking them causing an artifact. I have
not disputed this because it is not my place or in my job discription as a
traveler.  I am not even sure what it is supposed to look like or what type
of problems it causes.

Thanks for listening!
Deanna Leslie HT ASCP
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[Histonet] Rodent eye paraffin microtomy

2013-12-12 Thread b427297

I have a study coming up where obtaining perfect lens histology is critical.  
We do a pretty good job routinely, but since the lens is of interest, I would 
appreciate any tricks and techniques that can help us improve our paraffin lens 
histology within intact rodent eyes.
Thanks,
Jackie O'
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Re: [Histonet] Cutting issues

2013-12-12 Thread b427297

My educated guess would be that the tissues are being dried out prior to being 
placed in formalin at time of collection.  Surgeons are our biggest histology 
problems.
Jackie O'



-Original Message-
From: April P - Assocd apr...@associateddermhelena.com
To: histonet histonet@lists.utsouthwestern.edu
Sent: Thu, Dec 12, 2013 11:24 am
Subject: [Histonet] Cutting issues


Need feedback. We are a Derm lab
We are having an issue with some small punches and shaves being crushed or
arched. It does not happen every day and it is maybe one or two when it is
appening. Does anyone have any ideas on what can be causing this issue? 
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Re: [Histonet] histology tracking systems for pharma or contract lab

2013-12-05 Thread b427297
xybion is in the process of developing a histology module for Phama histo. We 
at AbbVie will be using this system. 
Jackie

Sent from my iPhone

 On Dec 5, 2013, at 13:23, Kim Merriam kmerriam2...@yahoo.com wrote:
 
 Hi,
 
 My company is considering a new tracking system for our histology studies.  
 This system needs to track everything from trimming, decal, embedding, 
 cutting, routine and molecular pathology/staining.  It also needs to be able 
 to accommodate complex study designs (multiple animals, groups, necropsy 
 timepoints, etc).
 
 I am interesting in hearing from people in other pharma/biotech/CROs to see 
 what they are using to capture this information.
 
 Thanks,
 Kim
  
 Kim Merriam, MA, HT(ASCP)QIHC
 Cambridge, MA
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Re: [Histonet] coverslipping question

2013-11-14 Thread b427297

Are you using tape or glass coverslips?  We have found that when using tape 
coverslips, at least two very clean 100% alcohol steps must be added before 
slides go into the clearing reagent, be it xylene or Histoclear.  If not, brown 
spots appear on some tissues, usually liver and bone.  If there is any TRACE of 
water retained in the tissue, it will show up as a brown artifact on the 
tissue.  This doesn't happen with conventional glass coverslipping and mounting 
medium - I think the mounting medium compensates for the retained moisture in 
the tissues.
Jackie


-Original Message-
From: Kim Donadio one_angel_sec...@yahoo.com
To: Gautier, Nicole M. nga...@lsuhsc.edu
Cc: histonet histonet@lists.utsouthwestern.edu
Sent: Wed, Nov 13, 2013 1:37 pm
Subject: Re: [Histonet] coverslipping question


I would try adding 1 or 2 more 100% alcohols before the histoclear. 

Sent from my iPhone

On Nov 12, 2013, at 9:32 AM, Gautier, Nicole M. nga...@lsuhsc.edu wrote:

 My lab has been having a problem with specks appearing on our slides after 
they come out of Histoclear.  Our protocol is to dehydrate in 2 minutes each of 
70%, 80%, 95%, and 100% ethanol before 2 minutes 2 times in Histoclear.  The 
slides are perfectly clear when they come out of the ethanols, but not when 
they 
come out of the Histoclear.
 Since it's not a problem we had when we first started, I tried changing out 
the Histoclear, but the problem remained.  At the end of last week, I changed 
out everything - all glassware, all ethanols, all Histoclear.  The problem went 
away and the 24 slides looked fine.  Today, the slides are looking speckled 
again.
 So I guess my questions are: What could be causing the speckled appearance of 
the slides? and  How often should I have to change the ethanols and Histoclear? 
 
I seem to remember years ago when I did this that we only changed the solutions 
monthly...
 
 Nicky Gautier
 Research Associate
 
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Re: [Histonet] processing eyes

2013-08-08 Thread b427297
We transfer eyes out of Mod Davidsons after 24 hours and process with the other 
soft tissues in formalin- why transfer to alcohol? We have beautiful  eye 
sections.
Jackie O'

Sent from my iPhone

On Aug 8, 2013, at 3:12 PM, Bea DeBrosse-Serra bdebrosse-se...@isisph.com 
wrote:

 Patsy, 
 
 18-24 hours in Davidson's followed by 70% ethanol prior to processing. Some 
 people also store the eyes in 10%NBF. I will attach a schedule for you off 
 line. 
 
 Bea
 
 Beatrice DeBrosse-Serra HT(ASCP)QIHC
 Isis Pharmaceuticals
 Antisense Drug Discovery
 2855 Gazelle Ct.
 Carlsbad, CA 92010
 760-603-2371
 
 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
 pru...@ihctech.net
 Sent: Thursday, August 08, 2013 1:06 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] processing eyes
 
 
 Can someone direct me to a protocol for processing eyes which have been 
 injected with Davidson's fixative and are now in 10% NBF.  We had an eye 
 expert at the U for years I was going to send my techs to but apparently she 
 has finally retired because we cannot get a hold of her.  Where are you Mary 
 Jo?
 
 
 We need insight on how to process non-human primate eyes? They have been 
 injected with Davidson's fixative and are now in 10%NBF. We need a specific 
 processing schedule, embedding and sectioning advice.
 
 
 
 Thank you,
 
 
 
 Patsy
 
 
 
 
 
 
 
 
 
 Patsy Ruegg, HT(ASCP)QIHC
 Ruegg IHC Consulting
 
 40864 E. Arkansas Ave
 
 Bennett, CO 80102
 
 H 303-644-4538
 
 C 720-281-5406
 
 mailto:prueg...@hotmail.com prueg...@hotmail.com 
 
 mailto:rueggihcconsultin...@outlook.com rueggihcconsultin...@outlook.com
 
 
 
 
 
 
 
 
 
 
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Re: [Histonet] monkey control slides

2012-10-25 Thread b427297
It depends on the species. All monkeys are not created equal. Some primaries 
work on Rhesus but not Cyno.

Sent from my iPhone

On Oct 25, 2012, at 12:54 PM, Eric Hoy eric@utsouthwestern.edu wrote:

 Amy,
 
 Try MeDiCa in Carlsbad, CA.  They have a variety of animal tissues for
 autoantibody detection.
 
 Their website, which is not very helpful, but will give you contact info:
 
 http://www.medica-dx.com
 
 Let me know if you can't get in touch with them.
 
 Eric Hoy
 
 ===
 Eric S. Hoy, Ph.D., SI(ASCP)
 Clinical Associate Professor
 Department of Medical Laboratory Sciences
 The University of Texas Southwestern Medical Center
 Dallas, Texas
 Email: eric@utsouthwestern.edu
 ===
 
 
 On 10/25/12 5:29 PM, Amy Lee amylee...@yahoo.com wrote:
 
 Hello,
  
 I was asked to do IHC on monkey atrium, kidney and spleen or liver tissue.
 Could anybody tell me which company carry these monkey slides?
  
 Thanks!
  
 Amy
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[Histonet] Gross macro digital camera

2012-06-28 Thread b427297
Would appreciate suggestions for a good digital camera for taking macro photos 
during necropsy. Any takers? Thanks much.
Jackie O'
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Re: [Histonet] Neutrophil Antibodies

2012-05-05 Thread b427297
While on the topic of neuts-anyone have an antibody for canine neutrphils in 
ffpe?

Sent from my iPhone

On May 5, 2012, at 9:59 AM, John Shelley jshel...@sanfordburnham.org wrote:

 Hi All in Histoland,
 
 Problem solving never ends! I am working up two antibodies for neutrophils 
 which are NIMP-R14 from Abcam which it is a rat monoclonal and also 
 Anti-Neutrophil Elastase also from Abcam but this is a Rb polyclonal. I have 
 tried different conditions without any luck and was wondering if anyone has 
 worked with these antibodies either from Abcam or another supplier and might 
 have working conditions that have given results in the past. We are trying 
 this on FFPE sections which the antibodies say they work on but I am thinking 
 that I may try frozens. I was trying to avoid this however because I am using 
 these antibodies on mouse WAT. Any help would be appreciated. Thanks!!!
 
 Happy Monday morning!!!
 Kind Regards!
 John J Shelley
 
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Re: [Histonet] Unregistered HT testing

2012-04-18 Thread b427297
The pathologist is interpreting the staining result, right? The HT is only 
evaluating the stain quality, not the results.

Sent from my iPhone

On Apr 18, 2012, at 9:43 AM, Dessoye, Michael J 
mjdess...@commonwealthhealth.net wrote:

 Our interpretation of special stains/IHC/ISH is that it is the
 'interpretation' of these stains that is 'high complexity'.  I believe
 that CLIA is the place where 'high complexity' is defined (although CAP
 may expand on this) and CLIA does not recognize ASCP registration.
 
 Michael J. Dessoye, M.S. | Histology Supervisor | Wilkes-Barre General
 Hospital | An Affiliate of Commonwealth Health |
 mjdess...@commonwealthhealth.net | 575 N. River Street | Wilkes Barre,
 PA 18764 | Tel: 570-552-1432 | Fax: 570-552-1526 
 
 
 -Original Message-
 From: Konop, Nicole [mailto:nko...@chw.org] 
 Sent: Tuesday, April 17, 2012 3:37 PM
 To: 'histonet@lists.utsouthwestern.edu'
 Subject: [Histonet] Unregistered HT testing
 
 Hello everyone!
 
 I'm just curious to know if anyone is allowing unregistered HT's to do
 special stains in their CAP accredited lab?  I have been involved in
 discussions regarding high complexity testing.  From the feedback I have
 received, special stains and IHC stains are considered high complexity
 testing.  I beg to disagree.  I can understand IHC/ISH as high
 complexity but I don't think routine special stains fall under that
 category.  I'd appreciate any feedback or literature you can reference
 for me to review.  Thank you!
 
 Nicole Anne Konop BS, HTL(ASCP)
 Histology Team Lead
 Children's Hospital of Wisconsin
 (414)266-6580 Direct Line
 (414)907-0366 Pager
 (414)266-2524 Histology Department
 
 
 
 
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[Histonet] Shipping prepared histology slides

2011-08-10 Thread b427297

Can someone provide a quick reference to ANYTHING I can use to prove to my EHS 
that fixed, processed, coverslipped slides are not HAZMAT?
They insist shipping finished slides cannot be performed by histotechs.  Wha?
Thanks.



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[Histonet] Vet tissue processing

2009-07-23 Thread B427297
I'm looking for a histology processing lab who will process NBF  veterinary 
tissues to H+E slides.  I need a short turn around time,  like 7-10 days.  
Any suggestions will be considered.
Thanks,
 
**Dell Deals: Treat yourself to a sweet deal on popular 
laptops! 
(http://pr.atwola.com/promoclk/100126575x1223100673x1201716527/aol?redir=http:%2F%2Faltfarm.mediaplex.com%2Fad%2Fck%2F12309%2D81939%2D1629%2D7)
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