Re: [Histonet] Cell block preparations

2020-01-16 Thread Tony Henwood (SCHN) via Histonet
Hi Jennifer,

I have had excellent success with lysing the red blood cells (using  Isotonic 
Ammonium Chloride) prior to cell block preparation with thromboplastin-plasma. 
The lysing solution contains EDTA so you will need to add a few drops of 1% 
calcium chloride. Method as follows:

Lysis solution
Ammonium Chloride4.5g
Potassium carbonate  0.5g
EDTA 0.0186g
Distilled water  500mls

Method:
1.  Centrifuge bloody fluid.
2.  Remove supernatant and add equal volume of lysis solution.
3.  Resuspend and incubate for 5 minutes at 4oC.
4.  Centrifuge, if blood still remains, then repeat from step 2.
5. Rinse in Hanks or RPMI, centrifuge.
6.  Mix pellet in a few drops of plasma.
7. Add thromboplastin and a few drops  of 1% Calcium Chloride, mix gently 
and allow clot to form.
8. Add 10% buffered formalin and fix and process as usual.

Reference:  
Kuenen-Boumiester etal (1996) Acta Cytolog 40:475-479

If you donot use the plasma clot method for cell block preparation, then use 
your preferred method after step 5.
The lysis solution can also be purchased commercially from several companies 
(eg Biolegend). It is commonly used for sample preparation for flow cytometry. 
Check the SDS to make sure it does not contain formaldehyde.


-Original Message-
From: Mac Donald, Jennifer via Histonet 
[mailto:histonet@lists.utsouthwestern.edu] 
Sent: Friday, 17 January 2020 4:53 AM
To: Charles Riley ; Histo List 

Subject: Re: [Histonet] Cell block preparations

Acetic acid would work.

Get Outlook for iOS 
From: Charles Riley via Histonet 
Sent: Thursday, January 16, 2020 8:55:21 AM
To: Histo List 
Subject: [Histonet] Cell block preparations

  EXTERNAL SENDER- Exercise caution with requests, links, and attachments.

What is the best way to remove excess blood from FNA sample collections before 
spinning them down into cell blocks?

--

Charles Riley BS  HT, HTL(ASCP)CM

Histopathology Coordinator/ Mohs
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Re: [Histonet] Coverslipper

2020-01-16 Thread Margaryan, Naira via Histonet
Happy Thursday, 

We would like to sell our slightly used but in excellent condition Dako 
Coverslipper which was purchased in 2010 (purchase price was $ 25K). The 
instrument can handle up to 600 slides per hour making it one of the fastest on 
the market. In addition to the flexibility of the Coverslipper it is easy and 
straightforward to operate and cleaning and maintenance is simple to do. It is 
small enough to fit into fume cabinets, easy to move around and accepts a 
variety of commercial mounting media.

Picture by request.

Will take any offer,
Naira


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[Histonet] RVU for Histology

2020-01-16 Thread Heckford, Karen - SMMC-SF via Histonet
Good Morning,
I think we are getting the short end of the stick when it is coming to 
productivity.   Can anyone give me insight on how they are calculating their 
RVU's for productivity in the Histology Lab?   I am busy as all get out and 
administration is saying our productivity is low.

Thanks,

Karen Heckford HT ASCP CE
Lead Histology Technician
St. Mary's Medical Center
450 Stanyan St.
San Francisco, Ca. 94117
415-668-1000 ext. 6167
karen.heckf...@dignityhealth.org

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[Histonet] needing IHC contol tissue

2020-01-16 Thread LeRoy Brown via Histonet
Would anyone happen to have a small pc of normal stomach they are willing to
part with for my IHC control for GAS6 stain?

Please let me know at 1...@comcast.net  

Thanks

LeRoy Brown HT(ASCP) HTL

 

 

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Re: [Histonet] H&E trouble shooting

2020-01-16 Thread Bert Dotson via Histonet
Excessive heat during slide drying can look like this but I think Liz has the 
most likely culprit. More specifically I would say there has been water 
carryover into your first clearing station during processing. Reagents not 
changed frequently enough or a low-grade mistakenly placed where 100% should 
be. Regards, Bert


-Original Message-
From: Liz Chlipala  
Sent: Wednesday, January 15, 2020 1:49 PM
To: Wang, Weixi 
Cc: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] H&E trouble shooting

That an image of incomplete dehydration the samples have not been processed 
properly and adequately dehydrated.

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

From: Wang, Weixi via Histonet 
Sent: Wednesday, January 15, 2020 11:20 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] H&E trouble shooting

Hi,
I have some issues on the staining quality of biopsies. Please see the image 
link below, the overall staining looks good but the edge looks weird, no 
nuclear staining picked up. Under-fixed? Over-dehydrated in the processor? Or 
dried during grossing?
You expertise is greatly appreciated!

https://urldefense.proofpoint.com/v2/url?u=https-3A__imgur.com_gallery_kpLqRT9&d=DwIFAg&c=imBPVzF25OnBgGmVOlcsiEgHoG1i6YHLR0Sj_gZ4adc&r=IkXb8WHm-SU8QcloSa5zh99VMreL429Dgfd2s0o3mrA&m=9Zt4pLGTo6dCvnjHleUlTkBYb8LQQc2G52vrJRkdg9M&s=8qzwuTTHy5TnitTfvT39e_57wxXJFJ2nygQXLWjNxVo&e=
 



Thank you,
Weixi




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Re: [Histonet] Cell block preparations

2020-01-16 Thread Mac Donald, Jennifer via Histonet
Acetic acid would work.

Get Outlook for iOS

From: Charles Riley via Histonet 
Sent: Thursday, January 16, 2020 8:55:21 AM
To: Histo List 
Subject: [Histonet] Cell block preparations

  EXTERNAL SENDER- Exercise caution with requests, links, and attachments.

What is the best way to remove excess blood from FNA sample collections
before spinning them down into cell blocks?

--

Charles Riley BS  HT, HTL(ASCP)CM

Histopathology Coordinator/ Mohs
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[Histonet] Cell block preparations

2020-01-16 Thread Charles Riley via Histonet
What is the best way to remove excess blood from FNA sample collections
before spinning them down into cell blocks?

-- 

Charles Riley BS  HT, HTL(ASCP)CM

Histopathology Coordinator/ Mohs
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[Histonet] Histotech openings

2020-01-16 Thread Katherine Marano via Histonet
Hi histonetters~

I'm working with a top laboratory in a beautiful area of North Carolina
that is looking to hire histotechs. They currently have 2 positions open.
The hours are varied from 10 pm – 12 noon. They’ll either be 3rd shift or a
split 3rd/1st shift. Permanent positions with great benefits.

Let me know if you are interested in hearing more!

Sincerely,

Katherine Marano
*K.A. Recruiting, Inc.*
Your Partner in Healthcare Recruiting
10 Post Office Square, 8th Floor So.
Boston, MA 02109
P:  (617) 746-2750
F:  (617) 507-8009
kather...@ka-recruiting.com
http://www.ka-recruiting.com
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