RE: [Histonet] Levels for Gastic and Esophogeal Bx's

2015-01-09 Thread Weems, Joyce K.
And I should have added that we do two unstained at level 2 - if needed for 
alcian blue/PAS and H. pylori on all gastrics. We only do them when ordered.

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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-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, Timothy
Sent: Friday, January 09, 2015 11:07 AM
To: 'Eileen Akemi Allison'; Histonet
Subject: RE: [Histonet] Levels for Gastic and Esophogeal Bx's

Akemi, it is really up to the pathologists to decide what they want. In some 
cases there is literature promoting certain standards (e.g, Hirschprung's) but 
in most cases it is just the comfort level of the person reviewing the case. We 
have a large variety of levels and unstained protocols but for standard 
biopsies it is two levels on one slide, no unstained. We only cut unstained if 
they are ordered as part of a protocol or ordered specifically. We do not cut 
extra unstained just in case. We had tens of thousands of unstained slides 
sitting in files just in case so I convinced them to stop that practice.

Tim Morken
Supervisor, Histology, Electron Microscopy and Neuromuscular Special Studies UC 
San Francisco Medical Center San Francisco, CA

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-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Eileen Akemi 
Allison
Sent: Friday, January 09, 2015 6:07 AM
To: Histonet
Subject: [Histonet] Levels for Gastic and Esophogeal Bx's

Good morning Histoland:

Happy Friday!  I believe this question was asked last year, but I would like to 
revisit this again. I have worked in a variety of laboratories in my career, 
both small and large. Most of my experience was in Oregon with large hospital 
laboratories and University institutions. Back then, we cut (6) levels on all 
our bx’s, and picked-up (2) sections on each level.  My current facility is 
cutting (3) levels and picking up (1) section on each level.

I would like to ask what everyone else is doing.  The reason I am asking is 
because our pathology director is requesting a change in our protocol to cut 
only (2) levels and (1) section at each level.

Sincerely,

Akemi Allison BS, HT/HTL (ASCP)

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RE: [Histonet] Levels for Gastic and Esophogeal Bx's

2015-01-09 Thread Morken, Timothy
Akemi, it is really up to the pathologists to decide what they want. In some 
cases there is literature promoting certain standards (e.g, Hirschprung's) but 
in most cases it is just the comfort level of the person reviewing the case. We 
have a large variety of levels and unstained protocols but for standard 
biopsies it is two levels on one slide, no unstained. We only cut unstained if 
they are ordered as part of a protocol or ordered specifically. We do not cut 
extra unstained just in case. We had tens of thousands of unstained slides 
sitting in files just in case so I convinced them to stop that practice. 

Tim Morken
Supervisor, Histology, Electron Microscopy and Neuromuscular Special Studies
UC San Francisco Medical Center
San Francisco, CA

CONFIDENTIALITY NOTICE: This email message, including any attachments, is for 
the sole use of the intended recipient(s) and may contain confidential, 
proprietary, and/or privileged information protected by law. If you are not the 
intended recipient, you may not use, copy, or distribute this email message or 
its attachments. If you believe you have received this email message in error, 
please contact the sender by reply email and destroy all copies of the original 
message.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Eileen Akemi 
Allison
Sent: Friday, January 09, 2015 6:07 AM
To: Histonet
Subject: [Histonet] Levels for Gastic and Esophogeal Bx's

Good morning Histoland:

Happy Friday!  I believe this question was asked last year, but I would like to 
revisit this again. I have worked in a variety of laboratories in my career, 
both small and large. Most of my experience was in Oregon with large hospital 
laboratories and University institutions. Back then, we cut (6) levels on all 
our bx’s, and picked-up (2) sections on each level.  My current facility is 
cutting (3) levels and picking up (1) section on each level.

I would like to ask what everyone else is doing.  The reason I am asking is 
because our pathology director is requesting a change in our protocol to cut 
only (2) levels and (1) section at each level.

Sincerely,

Akemi Allison BS, HT/HTL (ASCP)

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[Histonet] Slide and cassette labelers

2015-01-09 Thread Kim Shevlin
Hi Jim,
I do not have experience with the Tissue Tex Smartwrite, but I have used the 
Leica and Thermoscientific printers. Of the two, I prefer the Leica brand 
cassette and slide printers. The barcodes and human readable are crystal clear.

Hope this helps.
Kim

Kim Shevlin, HT ASCP
Histology and Pathology Operations Manager
Seventh Wave Laboratories, LLC
743 Spirit 40 Park Drive, Suite 108
Chesterfield, MO 63005
kshev...@7thwavelabs.commailto:kshev...@7thwavelabs.com
www.7thwavelabs.comhttp://www.7thwavelabs.com
636.519.4885 (Main Phone)
636.519.4776 (Histology Lab)
618.570.9383 (Cell Phone)

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RE: [Histonet] Automatic H E slide stainer recommendations

2015-01-09 Thread Sohrab,Behnaz
I agree


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of 
histot...@imagesbyhopper.com [histot...@imagesbyhopper.com]
Sent: Friday, January 09, 2015 3:37 AM
To: ian bernard
Cc: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Automatic H  E slide stainer recommendations

I second the Leica XL.  That stainer is a reliable workhorse.

Sent from my iPhone

On Jan 7, 2015, at 8:08 PM, ian bernard ian.bern...@comcast.net wrote:

The Leica Autostainer XL has proven effective for our lab.

IRB

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Conway, Carla
Sent: Tuesday, January 06, 2015 2:24 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Automatic H  E slide stainer recommendations

Hello colleagues,

I would appreciate any recommendations for an automatic slide stainer. It will 
primarily be used for H  E staining, not IHC.

Thanks in advance,

Carla







Carla Conway
Histology Technician
Western Fisheries Research Center, USGS
6505 N.E. 65th Street
Seattle, WA 98115-5016 USA
Phone: 206-526-2042
Fax: 206-526-6654
E-mail: cmcon...@usgs.gov
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RE: [Histonet] Automatic H E slide stainer recommendations

2015-01-09 Thread Sanders, Jeanine (CDC/OID/NCEZID)
Agree

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
histot...@imagesbyhopper.com
Sent: Friday, January 09, 2015 6:37 AM
To: ian bernard
Cc: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Automatic H  E slide stainer recommendations

I second the Leica XL.  That stainer is a reliable workhorse.

Sent from my iPhone

On Jan 7, 2015, at 8:08 PM, ian bernard ian.bern...@comcast.net wrote:

The Leica Autostainer XL has proven effective for our lab.

IRB

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Conway, Carla
Sent: Tuesday, January 06, 2015 2:24 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Automatic H  E slide stainer recommendations

Hello colleagues,

I would appreciate any recommendations for an automatic slide stainer. It will 
primarily be used for H  E staining, not IHC.

Thanks in advance,

Carla







Carla Conway
Histology Technician
Western Fisheries Research Center, USGS
6505 N.E. 65th Street
Seattle, WA 98115-5016 USA
Phone: 206-526-2042
Fax: 206-526-6654
E-mail: cmcon...@usgs.gov
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Re: [Histonet] Anyone using Biogenex stainers

2015-01-09 Thread Wendy L Roberts
Hi Everyone, 

Our lab has just inherited an old Leica cryostat (2800 Frigocut-E), which uses 
the disc style specimen stages (no post).  I've contacted Leica, but they no 
longer sell them, and the person I spoke to suggested that I contact this list 
for ideas.

Thanks in advance for any and all help!

Wendy

Wendy L Roberts

Research Analyst, Caron Lab
Department of Cell Biology
Duke University Medical Center
Box 3287 DUMC
Durham NC 27710

wendy.robe...@dm.duke.edu
919.681.4549


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[Histonet] Leica Aperio

2015-01-09 Thread Cynthia Robinson
Does anyone have experience setting up a report template for a breast panel on 
the Aperio? We just got ours set up and haven't had training yet. The thing has 
been here since November but with holidays and schedules not working it has 
been a trial. Are trying to get a jumpstart before the pathologists start 
training and think it should be ready to go immediately.



Thanks.



Cindi Robinson HT(ASCP)

Mercy Medical Center-Sioux City

Dunes Medical Laboratories

350 W Anchor Dr

Dakota Dunes SD 57049

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[Histonet] Bone Tissue in plastic embedding

2015-01-09 Thread Hernandez, Jesus Willibaldo
Dear Histonetter's,

Happy new year to everyone! I come today with a couple of questions regarding 
human bone embedded  in MMA:


1.   What is a good technique to dissolve the MMA from the tissue section? 
Also any suggestions on how to stain with HE?



2.   After mounting my tissue sections (5-10microns) with Haupts adhesive, 
I noticed that the bone within the section was appearing opaque/darkened on the 
microscope? Any suggestions on what this might be?

Thank you very much,

-Jesse H.
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[Histonet] And other crazy stuff.

2015-01-09 Thread Shirley A. Powell
Orangutan testicle macro section and alligator jawbones, not my best work, very 
humbling, after 52 years in the business.
Shirley 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, Timothy
Sent: Tuesday, January 06, 2015 2:24 PM
To: Patsy Ruegg; Roberta Horner; Douglas Gregg; Histonet@Lists. Edu
Subject: And other crazy stuff. RE: [Histonet] cutting honey bees

You crazy research people...OK, so what is the craziest thing you ever had to 
cut, or were asked to cut?

For me, not too bad, but embedding for EM and sectioning a single oocyte that 
was nearly microscopic. I'll just say it took a LOT of thick sections too face 
down to it without actually cutting through it.


Open the floodgates

Tim Morken

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Patsy Ruegg
Sent: Tuesday, January 06, 2015 11:13 AM
To: Roberta Horner; Douglas Gregg; Histonet@Lists. Edu
Subject: RE: [Histonet] cutting honey bees

for the whole bee I probably would process and embed it in glycol methacrylate 
(gma) it is much harder and would give better sections, we have done zebra fish 
and several other harder tissues including calcified bone in GMA.

Cheers,
Patsy

Patsy Ruegg, HT(ASCP)QIHC
Ruegg IHC Consulting
40864 E Arkansas Ave
Bennett, CO 80102
H 303-644-4538
C 720-281-5406
prueg...@hotmail.com



 From: r...@psu.edu
 To: classic...@gmail.com; histonet@lists.utsouthwestern.edu
 Date: Sat, 3 Jan 2015 23:15:33 +
 Subject: RE: [Histonet] cutting honey bees
 CC: 
 
 I sectioned and stained honey bee and yellow jacket stingers years ago.  They 
 wanted to show the difference between the stingers.  I wasn't sure what to do 
 so I processed and handled like everything else.  I was able to get some good 
 sections.  I put 6 stingers in each block and cut several sections figuring 
 there should be at least one good stinger in each block and it worked.
 Roberta Horner
 Penn State University
 Animal Diagnostic Lab
 
 From: histonet-boun...@lists.utsouthwestern.edu
 [histonet-boun...@lists.utsouthwestern.edu] on behalf of Douglas Gregg 
 [classic...@gmail.com]
 Sent: Saturday, January 03, 2015 6:08 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] cutting honey bees
 
 Has anyone had experience embedding and cutting honey bees. I am sure 
 there are some issues with the harder exoskeleton. Would that have to 
 be dissected away first. I am considering helping a student with a 
 science fair project on bees.
 
 Douglas Gregg
 Veterianary pathologist
 
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[Histonet] small biopsy protocol

2015-01-09 Thread Terri Braud
Hi Akemi – 

For what it is worth.  We used to cut small GI biopsies at 2 levels, 4 sections 
per level, per slide for HE, plus one extra unstained between levels.  We 
changed last year to 3 levels, 2 sections per level, all mounted on the same 
slide,  plus one extra unstained with 2 sections from between levels 2 and 3 on 
gastrics for possible H.Pylori stain.  For me, this is better because we are 
getting fewer requests for recuts.  I Hope this helps

Terri

 

Terri L. Braud, HT(ASCP)

Anatomic Pathology Supervisor

Holy Redeemer Hospital Laboratory

1648 Huntingdon Pike

Meadowbrook, PA 19046

Ph: 215-938-3676

Fax: 215-938-3874

 

Date: Fri, 9 Jan 2015 06:07:05 -0800

From: Eileen Akemi Allison akemiat3...@gmail.com

Subject: [Histonet] Levels for Gastic and Esophogeal Bx's

 

Good morning Histoland:

Happy Friday!  I believe this question was asked last year, but I would like to 
revisit this again. I have worked in a variety of laboratories in my career, 
both small and large. Most of my experience was in Oregon with large hospital 
laboratories and University institutions. Back then, we cut (6) levels on all 
our bx’s, and picked-up (2) sections on each level.  My current facility is 
cutting (3) levels and picking up (1) section on each level.

I would like to ask what everyone else is doing.  The reason I am asking is 
because our pathology director is requesting a change in our protocol to cut 
only (2) levels and (1) section at each level.

Sincerely,

Akemi Allison BS, HT/HTL (ASCP)

 

 


-



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[Histonet] PAS rx

2015-01-09 Thread Jennifer MacDonald
Some PAS procedures call for sulphurous rinses after the Schiffs reagent. 
From your experience is there a noticeable difference if you do not do the 
rinse?  Would it matter if you used sodium metabisulfite rather than 
potassium metabisulfite? 
Thank,
Jennifer
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RE: [Histonet] Automatic H E slide stainer recommendations

2015-01-09 Thread Bernice Frederick
I agree as well. The XL is a wokhorse. We have the transfer station and the 
CV5030 to go with it.

Bernice Frederick (HTL) ASCP
Senior Research Tech
Pathology Core Facility
Robert H. Lurie Cancer Center
Northwestern University
710 North Fairbanks Court
Olson Room 8421
Chicago, IL 60611
312-503-3723
b-freder...@northwestern.edu


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of 
histot...@imagesbyhopper.com [histot...@imagesbyhopper.com]
Sent: Friday, January 09, 2015 5:37 AM
To: ian bernard
Cc: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Automatic H  E slide stainer recommendations

I second the Leica XL.  That stainer is a reliable workhorse.

Sent from my iPhone

On Jan 7, 2015, at 8:08 PM, ian bernard ian.bern...@comcast.net wrote:

The Leica Autostainer XL has proven effective for our lab.

IRB

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Conway, Carla
Sent: Tuesday, January 06, 2015 2:24 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Automatic H  E slide stainer recommendations

Hello colleagues,

I would appreciate any recommendations for an automatic slide stainer. It will 
primarily be used for H  E staining, not IHC.

Thanks in advance,

Carla







Carla Conway
Histology Technician
Western Fisheries Research Center, USGS
6505 N.E. 65th Street
Seattle, WA 98115-5016 USA
Phone: 206-526-2042
Fax: 206-526-6654
E-mail: cmcon...@usgs.gov
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Re: [Histonet] And other crazy stuff.

2015-01-09 Thread Hans B Snyder
 You crazy research people...OK, so what is the craziest thing you
ever had to cut, or were asked to cut?

For me, I work in a research facility where I do everything.  One day
a botanist emailed me to cut pine on the cryostat and asked what the
largest size should be.  I told him 2 mm x 2mm and explained the
process as he had no idea what I was going to do. I thought ok, what
is pine?  He brought 5 pieces of wood pieces (pine) and asked if they
could be cut cross section at 10um with 5 sections per slide.  Of
course this is not something I have ever had expience in doing, and
they are hard as a rock.  The trick that ended up working, was to soak
the wood in warm water for 30 minutes, embed in OCT and cut.  After
cutting the sections were all balled up, so I floated them on water
and picked them up on the slide.  The sections were still folded and
looked horiffic in my mind but he loved them.  He said was going to
look at them under a Raman confocal and wanted to see the plant cell
wall.
Hans B Snyder
Histologistics
60 Prescott Street
Worcester, MA 01605
508-308-7800
h...@histologistics.com


On Fri, Jan 9, 2015 at 2:39 PM, Shirley A. Powell powell...@mercer.edu wrote:
 Orangutan testicle macro section and alligator jawbones, not my best work, 
 very humbling, after 52 years in the business.
 Shirley


 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, 
 Timothy
 Sent: Tuesday, January 06, 2015 2:24 PM
 To: Patsy Ruegg; Roberta Horner; Douglas Gregg; Histonet@Lists. Edu
 Subject: And other crazy stuff. RE: [Histonet] cutting honey bees

 You crazy research people...OK, so what is the craziest thing you ever had to 
 cut, or were asked to cut?

 For me, not too bad, but embedding for EM and sectioning a single oocyte that 
 was nearly microscopic. I'll just say it took a LOT of thick sections too 
 face down to it without actually cutting through it.


 Open the floodgates

 Tim Morken

 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Patsy Ruegg
 Sent: Tuesday, January 06, 2015 11:13 AM
 To: Roberta Horner; Douglas Gregg; Histonet@Lists. Edu
 Subject: RE: [Histonet] cutting honey bees

 for the whole bee I probably would process and embed it in glycol 
 methacrylate (gma) it is much harder and would give better sections, we have 
 done zebra fish and several other harder tissues including calcified bone in 
 GMA.

 Cheers,
 Patsy

 Patsy Ruegg, HT(ASCP)QIHC
 Ruegg IHC Consulting
 40864 E Arkansas Ave
 Bennett, CO 80102
 H 303-644-4538
 C 720-281-5406
 prueg...@hotmail.com



 From: r...@psu.edu
 To: classic...@gmail.com; histonet@lists.utsouthwestern.edu
 Date: Sat, 3 Jan 2015 23:15:33 +
 Subject: RE: [Histonet] cutting honey bees
 CC:

 I sectioned and stained honey bee and yellow jacket stingers years ago.  
 They wanted to show the difference between the stingers.  I wasn't sure what 
 to do so I processed and handled like everything else.  I was able to get 
 some good sections.  I put 6 stingers in each block and cut several sections 
 figuring there should be at least one good stinger in each block and it 
 worked.
 Roberta Horner
 Penn State University
 Animal Diagnostic Lab
 
 From: histonet-boun...@lists.utsouthwestern.edu
 [histonet-boun...@lists.utsouthwestern.edu] on behalf of Douglas Gregg
 [classic...@gmail.com]
 Sent: Saturday, January 03, 2015 6:08 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] cutting honey bees

 Has anyone had experience embedding and cutting honey bees. I am sure
 there are some issues with the harder exoskeleton. Would that have to
 be dissected away first. I am considering helping a student with a
 science fair project on bees.

 Douglas Gregg
 Veterianary pathologist

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Re: [Histonet] And other crazy stuff.

2015-01-09 Thread Paula Sicurello
I forgot to mention:   dirt

Happy Friday

Paula

On Fri, Jan 9, 2015 at 2:39 PM, Shirley A. Powell powell...@mercer.edu
wrote:

 Orangutan testicle macro section and alligator jawbones, not my best work,
 very humbling, after 52 years in the business.
 Shirley


 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu [mailto:
 histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, Timothy
 Sent: Tuesday, January 06, 2015 2:24 PM
 To: Patsy Ruegg; Roberta Horner; Douglas Gregg; Histonet@Lists. Edu
 Subject: And other crazy stuff. RE: [Histonet] cutting honey bees

 You crazy research people...OK, so what is the craziest thing you ever had
 to cut, or were asked to cut?

 For me, not too bad, but embedding for EM and sectioning a single oocyte
 that was nearly microscopic. I'll just say it took a LOT of thick sections
 too face down to it without actually cutting through it.


 Open the floodgates

 Tim Morken

 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu [mailto:
 histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Patsy Ruegg
 Sent: Tuesday, January 06, 2015 11:13 AM
 To: Roberta Horner; Douglas Gregg; Histonet@Lists. Edu
 Subject: RE: [Histonet] cutting honey bees

 for the whole bee I probably would process and embed it in glycol
 methacrylate (gma) it is much harder and would give better sections, we
 have done zebra fish and several other harder tissues including calcified
 bone in GMA.

 Cheers,
 Patsy

 Patsy Ruegg, HT(ASCP)QIHC
 Ruegg IHC Consulting
 40864 E Arkansas Ave
 Bennett, CO 80102
 H 303-644-4538
 C 720-281-5406
 prueg...@hotmail.com



  From: r...@psu.edu
  To: classic...@gmail.com; histonet@lists.utsouthwestern.edu
  Date: Sat, 3 Jan 2015 23:15:33 +
  Subject: RE: [Histonet] cutting honey bees
  CC:
 
  I sectioned and stained honey bee and yellow jacket stingers years ago.
 They wanted to show the difference between the stingers.  I wasn't sure
 what to do so I processed and handled like everything else.  I was able to
 get some good sections.  I put 6 stingers in each block and cut several
 sections figuring there should be at least one good stinger in each block
 and it worked.
  Roberta Horner
  Penn State University
  Animal Diagnostic Lab
  
  From: histonet-boun...@lists.utsouthwestern.edu
  [histonet-boun...@lists.utsouthwestern.edu] on behalf of Douglas Gregg
  [classic...@gmail.com]
  Sent: Saturday, January 03, 2015 6:08 PM
  To: histonet@lists.utsouthwestern.edu
  Subject: [Histonet] cutting honey bees
 
  Has anyone had experience embedding and cutting honey bees. I am sure
  there are some issues with the harder exoskeleton. Would that have to
  be dissected away first. I am considering helping a student with a
  science fair project on bees.
 
  Douglas Gregg
  Veterianary pathologist
 
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[Histonet] Levels for Gastic and Esophogeal Bx's

2015-01-09 Thread Eileen Akemi Allison
Good morning Histoland:

Happy Friday!  I believe this question was asked last year, but I would like to 
revisit this again. I have worked in a variety of laboratories in my career, 
both small and large. Most of my experience was in Oregon with large hospital 
laboratories and University institutions. Back then, we cut (6) levels on all 
our bx’s, and picked-up (2) sections on each level.  My current facility is 
cutting (3) levels and picking up (1) section on each level.

I would like to ask what everyone else is doing.  The reason I am asking is 
because our pathology director is requesting a change in our protocol to cut 
only (2) levels and (1) section at each level.

Sincerely,

Akemi Allison BS, HT/HTL (ASCP)

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RE: [Histonet] Levels for Gastic and Esophogeal Bx's

2015-01-09 Thread Marcum, Pamela A
We do 3 levels with no more than 2 sections per level.  It is what the 
pathologists prefer and therefore what we do.  

Pam Marcum 
UAMS

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Eileen Akemi 
Allison
Sent: Friday, January 09, 2015 8:07 AM
To: Histonet
Subject: [Histonet] Levels for Gastic and Esophogeal Bx's

Good morning Histoland:

Happy Friday!  I believe this question was asked last year, but I would like to 
revisit this again. I have worked in a variety of laboratories in my career, 
both small and large. Most of my experience was in Oregon with large hospital 
laboratories and University institutions. Back then, we cut (6) levels on all 
our bx’s, and picked-up (2) sections on each level.  My current facility is 
cutting (3) levels and picking up (1) section on each level.

I would like to ask what everyone else is doing.  The reason I am asking is 
because our pathology director is requesting a change in our protocol to cut 
only (2) levels and (1) section at each level.

Sincerely,

Akemi Allison BS, HT/HTL (ASCP)

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RE: And other crazy stuff. RE: [Histonet] cutting honey bees

2015-01-09 Thread Grantham, Andrea L - (algranth)
Shrew mandible, spittle bugs, white fly salivary glands, mosquito ovaries.

From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of Paula Sicurello 
[pat...@gmail.com]
Sent: Thursday, January 08, 2015 1:43 PM
To: Michael Ann Jones
Cc: histonet@lists.utsouthwestern.edu; Morken, Timothy; Roberta Horner; Douglas 
Gregg
Subject: Re: And other crazy stuff. RE: [Histonet] cutting honey bees

You asked for it:

squid tentacle tip, frog oocyte, serial sections through a entire zebra
fish embryo, honey bee eyes, harbor seal artery, Andean mummy muscle (flaky
little boogers), probably lots of others that I can't remember off the top
of my head.

Paula

On Thu, Jan 8, 2015 at 3:20 PM, Michael Ann Jones mjo...@metropath.com
wrote:

 We did a goldfish once, interesting microscopically and difficult for
 peeling (lots of keratin?)
 Michael Ann Jones, HT (ASCP)
 Histology Manager
 Metropath
 7444 W. Alaska Dr. #250
 Lakewood, CO 80226
 303.634.2511
 mjo...@metropath.com




 On 1/6/15, 12:23 PM, Morken, Timothy timothy.mor...@ucsf.edu wrote:

 You crazy research people...OK, so what is the craziest thing you ever
 had to cut, or were asked to cut?
 
 For me, not too bad, but embedding for EM and sectioning a single oocyte
 that was nearly microscopic. I'll just say it took a LOT of thick
 sections too face down to it without actually cutting through it.
 
 
 Open the floodgates
 
 Tim Morken
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Patsy
 Ruegg
 Sent: Tuesday, January 06, 2015 11:13 AM
 To: Roberta Horner; Douglas Gregg; Histonet@Lists. Edu
 Subject: RE: [Histonet] cutting honey bees
 
 for the whole bee I probably would process and embed it in glycol
 methacrylate (gma) it is much harder and would give better sections, we
 have done zebra fish and several other harder tissues including calcified
 bone in GMA.
 
 Cheers,
 Patsy
 
 Patsy Ruegg, HT(ASCP)QIHC
 Ruegg IHC Consulting
 40864 E Arkansas Ave
 Bennett, CO 80102
 H 303-644-4538
 C 720-281-5406
 prueg...@hotmail.com
 
 
 
  From: r...@psu.edu
  To: classic...@gmail.com; histonet@lists.utsouthwestern.edu
  Date: Sat, 3 Jan 2015 23:15:33 +
  Subject: RE: [Histonet] cutting honey bees
  CC:
 
  I sectioned and stained honey bee and yellow jacket stingers years ago.
  They wanted to show the difference between the stingers.  I wasn't sure
 what to do so I processed and handled like everything else.  I was able
 to get some good sections.  I put 6 stingers in each block and cut
 several sections figuring there should be at least one good stinger in
 each block and it worked.
  Roberta Horner
  Penn State University
  Animal Diagnostic Lab
  
  From: histonet-boun...@lists.utsouthwestern.edu
  [histonet-boun...@lists.utsouthwestern.edu] on behalf of Douglas Gregg
  [classic...@gmail.com]
  Sent: Saturday, January 03, 2015 6:08 PM
  To: histonet@lists.utsouthwestern.edu
  Subject: [Histonet] cutting honey bees
 
  Has anyone had experience embedding and cutting honey bees. I am sure
  there are some issues with the harder exoskeleton. Would that have to
  be dissected away first. I am considering helping a student with a
  science fair project on bees.
 
  Douglas Gregg
  Veterianary pathologist
 
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  Histonet mailing list
  Histonet@lists.utsouthwestern.edu
  http://lists.utsouthwestern.edu/mailman/listinfo/histonet
 
  ___
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  Histonet@lists.utsouthwestern.edu
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 Histonet mailing list
 Histonet@lists.utsouthwestern.edu
 http://lists.utsouthwestern.edu/mailman/listinfo/histonet
 
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 Histonet@lists.utsouthwestern.edu
 http://lists.utsouthwestern.edu/mailman/listinfo/histonet


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[Histonet] Tesr

2015-01-09 Thread histot...@imagesbyhopper.com
Please disregard 

Sent from my iPhone

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Re: [Histonet] Automatic H E slide stainer recommendations

2015-01-09 Thread histot...@imagesbyhopper.com
I second the Leica XL.  That stainer is a reliable workhorse.

Sent from my iPhone

On Jan 7, 2015, at 8:08 PM, ian bernard ian.bern...@comcast.net wrote:

The Leica Autostainer XL has proven effective for our lab.

IRB

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Conway, Carla
Sent: Tuesday, January 06, 2015 2:24 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Automatic H  E slide stainer recommendations

Hello colleagues,

I would appreciate any recommendations for an automatic slide stainer. It will 
primarily be used for H  E staining, not IHC.

Thanks in advance,

Carla







Carla Conway
Histology Technician
Western Fisheries Research Center, USGS
6505 N.E. 65th Street
Seattle, WA 98115-5016 USA
Phone: 206-526-2042
Fax: 206-526-6654
E-mail: cmcon...@usgs.gov
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RE: [Histonet] Levels for Gastic and Esophogeal Bx's

2015-01-09 Thread Weems, Joyce K.
Same here

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

This e-mail, including any attachments is the property of Saint Joseph’s 
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-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Marcum, Pamela A
Sent: Friday, January 09, 2015 9:34 AM
To: 'Eileen Akemi Allison'; Histonet
Subject: RE: [Histonet] Levels for Gastic and Esophogeal Bx's

We do 3 levels with no more than 2 sections per level.  It is what the 
pathologists prefer and therefore what we do.

Pam Marcum
UAMS

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Eileen Akemi 
Allison
Sent: Friday, January 09, 2015 8:07 AM
To: Histonet
Subject: [Histonet] Levels for Gastic and Esophogeal Bx's

Good morning Histoland:

Happy Friday!  I believe this question was asked last year, but I would like to 
revisit this again. I have worked in a variety of laboratories in my career, 
both small and large. Most of my experience was in Oregon with large hospital 
laboratories and University institutions. Back then, we cut (6) levels on all 
our bx’s, and picked-up (2) sections on each level.  My current facility is 
cutting (3) levels and picking up (1) section on each level.

I would like to ask what everyone else is doing.  The reason I am asking is 
because our pathology director is requesting a change in our protocol to cut 
only (2) levels and (1) section at each level.

Sincerely,

Akemi Allison BS, HT/HTL (ASCP)

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the sole use of the intended recipient(s) and may contain confidential and 
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contact the sender by reply e-mail and destroy all copies of the original 
message.



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