RE: [Histonet] Macrophage marker in sheep for IHC

2011-06-27 Thread Vivek Saroha
Thank you to everyone who has replied and given suggestions.

I now have some ideas to help me start and will update and acknowledge once 
again once I make some progress.


Best regards

Vivek

-Original Message-
From: Jan Shivers [mailto:shive...@umn.edu] 
Sent: 24 June 2011 14:37
To: Vivek Saroha; histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Macrophage marker in sheep for IHC

CD68 - clone KP1 has not worked on sheep (also not dogs, cows, horses, and 
chickens) in my experience.  I have found it to stain primates well (and 
rare cells in pigs and cats).

Jan Shivers
Senior Scientist
Histology/IHC/EM Section Head
Pathology Teaching Program
University of Minnesota
Veterinary Diagnostic Laboratory
1333 Gortner Ave.
St. Paul, MN  55108
612-624-7297
shive...@umn.edu

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think you have received this message in error, please advise the sender and 
then delete this message and any attachments immediately.)

- Original Message - 
From: Vivek Saroha vivek.sar...@nottingham.ac.uk
To: histonet@lists.utsouthwestern.edu
Sent: Friday, June 24, 2011 4:05 AM
Subject: [Histonet] Macrophage marker in sheep for IHC


Hi there,
I am very new to basic sciences research and am planning an experiment to 
quantify and compare adipose tissue macrophage infiltration in sheep model 
using immunohistochemistry. I am specifically interested in CD11c as a 
marker of M1 activation of Macrophages. I have been advised that it is not 
easy and previous effort by my predecessors have not been very successful in 
this!
From the general google, histonet/histosearch and pubmed search. I have 
made a list of potential candidates:

1.Clones PG M1 and Clone KP1
(Source : Histonet : 
http://www.histosearch.com/histonet/Nov03A/RE.HistonetSeepmacrophage.html)


2.EMB11, a mouse anti-human CD68 mAb (Dako, Carpenteria, CA)
(source: published paper: http://www.ncbi.nlm.nih.gov/pubmed/16460804 )


 1.  Another CD68 antibody
Source: 
http://www.ingentaconnect.com/content/ocean/ajra/2011/0025/0002/art00024)

 1.  Iba1 (ionized calcium binding adaptor molecule 1) is a 17-kDa EF hand 
protein that is specifically expressed in macrophages/microglia and is 
upregulated during the activation of these cells.[Wikipedia]
(source: I do not remember where I found this one from but Abcam has several 
antibodies none of which are predicted for sheep)
I am writing to ask for suggestions about which one to go for and any other 
tips about searching for antibodies or performing IHC in paraffin fixed 
adipose tissue/liver.
Any ideas will be gratefully appreciated as I am very new and isolated in 
this aspect.
Best wishes
Vivek

Dr Vivek Saroha
Clinical lecturer in Child health
University of Nottingham
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RE: [Histonet] Tissue Shriveling in Paraffin

2011-06-27 Thread sgoebel
You could have got the tissue wet or to hydrated.  Sometimes after you
face the block if you leave it on the ice to long and let moisture get
into the tissue then cut the slide, it looks ok at the time, but once
the moisture gets back out of the tissue it will start to look concave.
If you are going to be leaving your blocks on the ice for a long time
just put a 4X4 or paper towel under the block, this helps.
Good luck =)

Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas  78744
(512)901-0900 ext. 6912


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Michelle
Aono
Sent: Friday, June 24, 2011 8:28 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Tissue Shriveling in Paraffin

I was cutting some bone/joint tissue and noticed that the cartilaginous
portion was concave/indented, instead of flush with the rest of the
block surface.  Even as I continued to cut that portion always seemed a
little sunken into the block face and all the sections crumbled.  I
didn't seal the block after I was done and when I came back the next day
the entire tissue sample was shriveled and pulling away from the
paraffin.  I'm new, but in the few bone sections I've done I've never
had this happen!  Any ideas?

~Shelly

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RE: [Histonet] RE: HistoGel

2011-06-27 Thread sgoebel
You can also use agar.  It does the same thing and is cheaper =)

Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas  78744
(512)901-0900 ext. 6912


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Milne,
Katy
Sent: Friday, June 24, 2011 12:27 PM
To: 'histonet@lists.utsouthwestern.edu'; 'mjdess...@wvhcs.org'
Subject: [Histonet] RE: HistoGel

We use histogel a lot in our lab.  It's a research lab and we use it for
a few purposes - pelleting cultured cells then creating multi-culture
TMAs for testing antibodies and also pelleting cells from ascites and
pleural effusions.  Has also been used to process really small samples
that could have been lost in the processor through the cassettes.

Works quite well.  The researchers just put the samples in histogel and
give it to me in formalin then I process it as I would regular tissue.
Cuts very well too.

Katy


Message: 3
Date: Fri, 24 Jun 2011 12:26:46 -0400
From: Dessoye, Michael J mjdess...@wvhcs.org
Subject: [Histonet] HistoGel
To: histonet@lists.utsouthwestern.edu
Message-ID:

e2547e1cd0ee324488a2940994571efa0401f...@wvhcs-exchange.wvhcs.com
Content-Type: text/plain;   charset=iso-8859-1

Hello,
 
Does anyone out there have any experience with HistoGel?  It's Richard
Allan/Thermo Fisher.  They claim that you can embed scant tissues in
the gel and then process, embed, and cut as usual.  Just wondering how
it works in the real world
 
Michael J. Dessoye, M.S. | Histology Supervisor | Wyoming Valley Health
Care System | mjdess...@wvhcs.org mailto:mjdess...@wvhcs.org  |
575 N. River Street | Wilkes Barre, PA 18764 | Tel: 570-552-1485 | Fax:
570-552-1526 

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RE: [Histonet] bluing

2011-06-27 Thread sgoebel
Just add a little bit more ammonia hydroxide to the water =)  

Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas  78744
(512)901-0900 ext. 6912


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Webb,
Dorothy L
Sent: Friday, June 24, 2011 2:21 PM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] bluing

Looking to change my bluing step in the HE process to obtain a bluer
(less purple) hue to the nuclear detail.  What is everyone using in
their bluing step??

Thanks for all of your ideas!!



  
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RE: Re: [Histonet] How many tissues an histo tech is suppose to cutper

2011-06-27 Thread sgoebel
Another solution...get out of clinical and go into research =)  There are no 
quotas or slide per second expectations in the research world =)  So sorry you 
are having such a bad time with your job.  HT's are not a dime a dozen and 
usually it is fairly easy to find a better job.  Not to mention research pays 
almost double the clinical world!!
Good Luck!!

Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas  78744
(512)901-0900 ext. 6912


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rene J Buesa
Sent: Sunday, June 26, 2011 9:43 AM
To: histonet-requ...@lists.utsouthwestern.edu; histonet@lists.utsouthwestern.edu
Subject: Fw: Re: [Histonet] How many tissues an histo tech is suppose to cutper



---






Joanne:
Read the attachment so you can have an idea about productivity ranges and 
averages in different tasks in the lab.
If you embedded 214 blocks and cut 148  in 5.5 hours, using the averages I 
provided, embedding should have taken 3.5 hours and cutting 6.2 hours which 
means you worked 1.76 times FASTER than the expected average.
René J.

--- On Sat, 6/25/11, Joanne joanne0...@comcast.net wrote:


From: Joanne joanne0...@comcast.net
Subject: [Histonet] How many tissues an histo tech is suppose to cut per
To: histonet@lists.utsouthwestern.edu
Date: Saturday, June 25, 2011, 7:07 PM


i am quite serious in my presentation and request for advice.  i too thought 
this goal was/is ridiculous to expect/ask for from someone so new and to attain 
in 6 months or less.  last monday i embedded 214 blocks and cut 148 between 5am 
and 10:30am (we had almost 600 cassettes to share among 3 people) . . . .for 
someone so very new i thought this pretty good . . . please note: most days 
aren't as hectic.  :)  what is an average though for blocks/minute?  what is 
meant by set sum per block? ---keeping in mind i am new to this field.



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[Histonet] Full Time HT position in Oklahoma City Ok

2011-06-27 Thread Gaiser, Marcia
POSITION REQUIREMENTS:

EDUCATION:   High school diploma or GED preferred.

CERTIFICATION, LICENSURE, BONDING:  Certified as an HT or HLT by the American 
Society of Clinical Pathologists (ASCP) – or – other nationally recognized 
certifying agency acceptable to the Laboratory Director – or – experience 
acceptable to the Laboratory Director.

EXPERIENCE:  Two years of satisfactory histology experience.

SIGN ON BONUS AVAILABLE FOR QUALIFIED CANDIDATES.  Outstanding benefits package 
including generous paid time off.

Apply online at www.saintsok.comhttp://www.saintsok.com, Ad# 10762, or 
contact Anna King at (405) 272-6105 for more information.

Thank you!

Anna King
HR Recruiter
St. Anthony Hospital
(405) 272-6105 - phone
(405) 272-6781 - fax
[https://mobile.ssmhc.com/owa/attachment.ashx?id=RgBMsXdcX9YUQLcxZSN9Shu5BwByj4F8AhEOSY2AOnw7DGJIAAUpEpPHAAByj4F8AhEOSY2AOnw7DGJIAAaNIGfxAAAJattcnt=1attid0=EACRQxAfu%2f2MRrpel0TNLrK5]


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[Histonet] How many tissues...

2011-06-27 Thread Gagnon, Eric
To add to the recent discussion about how many blocks can be cut per hour, the 
College of Medical Laboratory Technologists of Ontario published Practice 
Guidelines for Medical Laboratory Technologists Practising in Histology fairly 
recently, in 2008, which may be of use in this context.  The practice 
guidelines are intended to support, not replace, the exercise of professional 
judgment by medical laboratory technologists practising in histology...and are 
maintained...in consultation with CMLTO members and stakeholders. 
 
The usual workplace variables are taken into account in the guideline, but at 
least there are some daily ranges presented which may help Joanne in her quest 
for a reasonable goal.  
 
Link follows:
http://tinyurl.com/histology-guidelines 
http://tinyurl.com/histology-guidelines 
 
Eric Gagnon MLT
Histology Laboratory
Kingston General Hospital
Kingston, Ontario

 
 


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[Histonet] One block per minute

2011-06-27 Thread madary

   It  seems like this argument has been going on as long as the histonet
   =  has  been here for us. Just because some folks in histoland can cut
   60  block=  s  per  minute  does  not  mean that should be the minimum
   standard, esp for a n= ew tech, come on that is just dangerous to make
   someone  that nervous. = When we purchase a car that states it gets 23
   mpg  city and 31 mpg on the hi= ghway, those are in perfect conditions
   when  all  the  stars  align,  going  down= hill in neutral.  These so
   called intutive managers who expect someone= to cut 60 blocks per hour
   clearly  never had a pack of blades that took thr= ee minutes to get a
   blade  to  slide  out,  never had a dull blade, no interrup= tions, no
   fire alarms,no call for levels, decals, only had perfect processi= ng,
   perfect soak etc. In 30 plus years I have heard so many people tell me
   =  they can do this, but have never witnessed such an incredible feat,
   day in = day out.



   Nick(Rocky) Madary, HT/HTL(ASCP)QIHC
   Jun 26, 2011 12:01:08 PM, = histonet@lists.utsouthwestern.edu wrote:

 Send Histonet= mailing list submissions to
 histonet@lists.utsouthwestern.edu
 To= subscribe or unsubscribe via the World Wide Web, visit
 http://lists.uts= outhwestern.edu/mailman/listinfo/histonet
 or, via email, send a message = with subject or body 'help' to
 histonet-requ...@lists.utsouthwestern.edu You can reach the person 
managing the list at
 histonet-owner@lis= ts.utsouthwestern.edu
 When  replying,  please  edit  your  Subject  line  s= o it is more
 specific
 than Re: Contents of Histonet digest...
 = BRToday's Topics:
 1. for phd offer (mani kandan)
 2. Leica Bond f= or IHCs (Nancy Schmitt)
 3. Re: Histonet Digest, Vol 91, Issue 34 (Amos B= rooks)
 4.  How many tissues an histo tech is suppose to cut per (Joanne) 
BR5. RE: How many tissues an histo tech is suppose to cut per
 (Rittman,= Barry R)
 6. How many tissues an histo tech is suppose to cut per (Joann= e)
 7. Re: How many tissues an histo tech is suppose to cut per
 (histo= t...@imagesbyhopper.com)
 8. RE: How many tissues an histo tech is suppos= e to cut per
 (Thomas Jasper)
 9. RE: Leica Bond for IHCs (Houston, Ron= ald)
 10. RE: How many tissues an histo tech is suppose to cut per
 (Th= omas Jasper)
 11. Re: How many tissues an histo tech is suppose to cut pe= r
 (Victoria Baker)
 12. Re: AL state meeting? (David Kemler)
 13. RE= : How many tissues an histo tech is suppose to cut per
 (WILLIAM DESALVO) 14. Re: How many tissues an histo tech is suppose to 
cut per
 (histot= e...@imagesbyhopper.com)
 15. RE: Leica Bond for IHCs (Horn, Hazel V)
 1= 6. Re: How many tissues an histo tech is suppose to cut per
 (Rene J Bues= a)
 17. Fw: Re: [Histonet] How many tissues an histo tech is suppose
 t= o cut per (Rene J Buesa)
 18.  Sakura  auto  TEC  and  the  Leica  cassette prin= ter (Denise
 Mattingly)
 - -
 Message: 1
 Date: Sat, 25 Jun 2011 2= 3:06:06 +0530 (IST)
 From: mani kandan
 Subject= : [Histonet] for phd offer
 To: histonet@lists.utsouthwestern.edu
 Mess= age-ID:
 1309023366.93666.yahoomailclas...@web94702.mail.in2.yahoo.co= m
 Content-Type: text/plain; charset=iso-8859-1
 Hai hist= onetters,
   n=  bsp;i  am  a  master  of  science graduate  
working  in  stemcell research,looking for a phd offer or RA offer,
 currently=  i  am  working  on  cell derived from bone enosteal and
 central  region cells. = i am looking for research offer related to
 this field. i am looking for fav= ourable reply. thank u.
 M.Manikandan,
 Researcher,
 Stemcell uni= t,
 King Saud university,
 Riyadh,KSA
 +966552012697
 -= -
 Message: 2
 Date: Sat, 25 Jun 2011 17:49:21 = +
 From: Nancy Schmitt
 Subject: [Histon= et] Leica Bond for IHCs
 To: histonet@lists.utsouthwestern.edu
 Message-ID:
 906B4DA90ED1DB4DB6C7E9= 4d7cee6c36790...@peitha.wad.pa-ucl.com
 Content-Type: text/plain; cha= rset=us-ascii
 We  are  very  happy with our BOND and technical supp= ort has been
 great for any and all questions/issues.
 Nancy Schmitt H= T,MLT(ASCP)
 Dubuque, IA
 --
 Message= : 16
 Date: Sat, 25 Jun 2011 12:00:44 -0400
 From: Sheila Adey
 Subject: [Histonet] Leica Bond for IHCs
 To:
 Message-ID:
 Content-Type: text/plain; charset=iso-8859-1
 Hello= netters:
 Looking for opinions on the Leica Bond immuno stainer please.  Thanks.
 Sheila
 NOTICE:  This  email  may contain legal= ly privileged information.
 The information
 is  for  the  use  of  only  the  in=  tended  recipient(s) even if
 

RE: [Histonet] How many tissues an histo tech is suppose to cut per

2011-06-27 Thread Morken, Timothy
The only time I have seen techs cut that fast was when there was a team - one 
cuts, the other picks up the section and labels the slides. These were Aussies 
and Kiwis I worked with overseas and that is how they work in some places. BTW, 
they also stand at the bench and put the microtome sideways in order to work 
faster (pull the ribbon off, throw it on the waterbath and go on to the next 
block. Otherwise, forget it, it is not possible and still keep quality and 
sanity intact.

Tim Morken
Supervisor, Histology, IPOX
UCSF Medical Center
San Francisco, CA, USA

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joanne
Sent: Saturday, June 25, 2011 2:50 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] How many tissues an histo tech is suppose to cut per


 
i've only been working 2 months.  although older, i am new as a histotech 
(graduated in may 2010, found a job in april 2011).  seems management is 
setting a goal of a block per minute as far as cutting goes for me.  i have 
until october to attain this goal. this minute for cutting is to include 
facing, writing out slides, cutting, and putting tray into symphony stainer 
(not to mention getting up to answer the phone, fielding questions regarding 
send-out cases, and other slight cutting interruptions).   this seems an 
extreme, possibly unattainable goal.  i'm up for a challenge  at age 53, but 
any advice would be SWONDERFUL :)   
 
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[Histonet] Interesting article on a Healthcare Camp to educate children on the healthcare professions.

2011-06-27 Thread Pam Barker
Hi Histonetters,
I found this article on a healthcare camp to educate kids on the
healthcare professions:
http://billingsgazette.com/news/state-and-regional/wyoming/article_06923
0e4-c77e-5b4d-95e0-bd9741f0595f.html

Have a great day!
 
Thank You!
 
 
Pam Barker
President
RELIA 
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  search Pam Barker RELIA
www.linkedin.com/reliasolutions
www.myspace.com/pamatrelia
www.twitter.com/pamatrelia 

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RE: [Histonet] How many tissues an histo tech is suppose to cut per

2011-06-27 Thread Weems, Joyce
At one place I worked we teamed like this and it was so efficient! It also 
helped with error reduction. 

The main problem I see for Joanne is the getting up to answer the phone, 
fielding questions regarding send-out cases, and other slight cutting 
interruptions. No one can predict how long these interruptions would take. 

Joanne, I think I would ask for uninterrupted time in the beginning to hone 
your cutting skills. As your confidence builds, so will your speed. And so will 
the time to refocus after an interruption. I rarely cut these days and when I 
do I am slower than slow. 

Best wishes, j


Joyce Weems 
Pathology Manager 
Saint Joseph's Hospital 
5665 Peachtree Dunwoody Rd NE 
Atlanta, GA 30342 
678-843-7376 - Phone 
678-843-7831 - Fax 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, Timothy
Sent: Monday, June 27, 2011 11:15
To: 'Joanne'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] How many tissues an histo tech is suppose to cut per

The only time I have seen techs cut that fast was when there was a team - one 
cuts, the other picks up the section and labels the slides. These were Aussies 
and Kiwis I worked with overseas and that is how they work in some places. BTW, 
they also stand at the bench and put the microtome sideways in order to work 
faster (pull the ribbon off, throw it on the waterbath and go on to the next 
block. Otherwise, forget it, it is not possible and still keep quality and 
sanity intact.

Tim Morken
Supervisor, Histology, IPOX
UCSF Medical Center
San Francisco, CA, USA

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joanne
Sent: Saturday, June 25, 2011 2:50 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] How many tissues an histo tech is suppose to cut per


 
i've only been working 2 months.  although older, i am new as a histotech 
(graduated in may 2010, found a job in april 2011).  seems management is 
setting a goal of a block per minute as far as cutting goes for me.  i have 
until october to attain this goal. this minute for cutting is to include 
facing, writing out slides, cutting, and putting tray into symphony stainer 
(not to mention getting up to answer the phone, fielding questions regarding 
send-out cases, and other slight cutting interruptions).   this seems an 
extreme, possibly unattainable goal.  i'm up for a challenge  at age 53, but 
any advice would be SWONDERFUL :)   
 
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[Histonet] Histogel Protocol FROZEN Histonet Digest, Vol 91, Issue 34

2011-06-27 Thread Kathy Bonness
Katy (or anyone else who has used Histogel for FROZEN samples),
  I am using Histogel mixed with OCT to create a frozen cell pellet.  I was 
successful with doing a single pellet but now I am being asked to do multiple 
and have found hit some challenges.
  I have never done a TMA but that sounds like a great option.  We are a 
research lab but using the Cell Pellet for a normalizing control of IF 
intensity (for computational analysis normalization for lung tissue) and one of 
the largest challenges is retaining cell density while still trying to 
cryoprotect and freeze well with the OCT surrounding it.
  Has anyone worked out a method for frozen cell pellets to embedded with 
multiple cell lines?  Most of what I have found has been from FFPE, any 
suggestions would be appreciated.
  Thank you!
Kathy

Kathy M. Bonness, PhD.



251-533-2661

kathy.bonn...@utsouthwestern.edu

http://www.linkedin.com/pub/kathy-bonness/6/1a1/931



UTSW  Dallas, TX

Green Center for Computational  Systems Biology

Department of Pharmacology

Altschuler/Wu Lab   (ND9.214)


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of 
histonet-requ...@lists.utsouthwestern.edu 
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Sent: Saturday, June 25, 2011 12:00 PM
To: histonet@lists.utsouthwestern.edu
Subject: Histonet Digest, Vol 91, Issue 34

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Today's Topics:

   1. RE: HistoGel (Milne, Katy)
   2. Histogel Problem (Amos Brooks)
   3. RE: Histogel Problem (Delossantos_Roseann)
   4. bluing (Webb, Dorothy L)
   5. Re: bluing (Rene J Buesa)
   6. RE: bluing (Harrison, Sandra C.)
   7. blades (Webb, Dorothy L)
   8. Re: blades (Sean McBride)
   9. Re: blades (Esther C Peters)
  10. Re: blades (Victoria Baker)
  11. Re: blades (Jennifer MacDonald)
  12. HT Position - Irvine, CA (Eric Velazquez)
  13. Re: HT Position - Irvine, CA (Lee  Peggy Wenk)
  14. Contents of Histonet digest (Aurea Marquez)
  15. Re: bluing (Lee  Peggy Wenk)
  16. Leica Bond for IHCs (Sheila Adey)
  17. RE:  Bluing  (gayle callis)


--

Message: 1
Date: Fri, 24 Jun 2011 10:27:09 -0700
From: Milne, Katy kmi...@bccancer.bc.ca
Subject: [Histonet] RE: HistoGel
To: 'histonet@lists.utsouthwestern.edu'
histonet@lists.utsouthwestern.edu,'mjdess...@wvhcs.org'
mjdess...@wvhcs.org
Message-ID:
3feff18ff4e1914a9ab7d8498591be8610cf058...@vexccr02.phsabc.ehcnet.ca
Content-Type: text/plain; charset=us-ascii

We use histogel a lot in our lab.  It's a research lab and we use it for a few 
purposes - pelleting cultured cells then creating multi-culture TMAs for 
testing antibodies and also pelleting cells from ascites and pleural effusions. 
 Has also been used to process really small samples that could have been lost 
in the processor through the cassettes.

Works quite well.  The researchers just put the samples in histogel and give it 
to me in formalin then I process it as I would regular tissue.  Cuts very well 
too.

Katy


Message: 3
Date: Fri, 24 Jun 2011 12:26:46 -0400
From: Dessoye, Michael J mjdess...@wvhcs.org
Subject: [Histonet] HistoGel
To: histonet@lists.utsouthwestern.edu
Message-ID:
e2547e1cd0ee324488a2940994571efa0401f...@wvhcs-exchange.wvhcs.com
Content-Type: text/plain;   charset=iso-8859-1

Hello,

Does anyone out there have any experience with HistoGel?  It's Richard 
Allan/Thermo Fisher.  They claim that you can embed scant tissues in the gel 
and then process, embed, and cut as usual.  Just wondering how it works in the 
real world

Michael J. Dessoye, M.S. | Histology Supervisor | Wyoming Valley Health Care 
System | mjdess...@wvhcs.org mailto:mjdess...@wvhcs.org  |
575 N. River Street | Wilkes Barre, PA 18764 | Tel: 570-552-1485 | Fax: 
570-552-1526



--

Message: 2
Date: Fri, 24 Jun 2011 13:29:09 -0400
From: Amos Brooks amosbro...@gmail.com
Subject: [Histonet] Histogel Problem
To: histonet@lists.utsouthwestern.edu
Message-ID: BANLkTinbTG=qcs3peuf8zfa3bz2wqrt...@mail.gmail.com
Content-Type: text/plain; charset=ISO-8859-1

Hi,
   I have a problem with some blocks that were prepared with Histogel. I was
hoping someone else might have had a similar problem and figured it out. I
took a photo of the blocks that were mads and put them in a Picassa album
here:

RE: [Histonet] How many tissues an histo tech is suppose to cut per

2011-06-27 Thread Blazek, Linda
Unless you are in some remote area that there aren't any other facilities 
around, I would look for a new job!  I don't think your age should have any 
bearing on finding one.  If you were close to me I'd hire you.  Working under 
that kind of condition is unacceptable in my opinion.  It promotes errors and 
that isn't what we are all about.  Those blocks are our patients.

Linda

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joanne
Sent: Saturday, June 25, 2011 2:50 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] How many tissues an histo tech is suppose to cut per


 
i've only been working 2 months.  although older, i am new as a histotech 
(graduated in may 2010, found a job in april 2011).  seems management is 
setting a goal of a block per minute as far as cutting goes for me.  i have 
until october to attain this goal. this minute for cutting is to include 
facing, writing out slides, cutting, and putting tray into symphony stainer 
(not to mention getting up to answer the phone, fielding questions regarding 
send-out cases, and other slight cutting interruptions).   this seems an 
extreme, possibly unattainable goal.  i'm up for a challenge  at age 53, but 
any advice would be SWONDERFUL :)   
 
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RE: [Histonet] How many tissues an histo tech is suppose to cut per

2011-06-27 Thread Garcia, Lori, Sr. Scientist
 I agree with Tim. I have been in the field for over 20 years, and this is an 
unrealistic goal even for a veteran. Your manager obviously has no experience 
or understanding of your job in order to set that type of goal for you. It 
would be possible if the blocks are already chilled, the slides pre-labeled, 
and you have a helper to load the slides in the racks and onto the stainer. 
Even then there will be some sacrifice of quality for quantity. Just my two 
cents.

Lori

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, Timothy
Sent: Monday, June 27, 2011 8:15 AM
To: 'Joanne'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] How many tissues an histo tech is suppose to cut per

The only time I have seen techs cut that fast was when there was a team - one 
cuts, the other picks up the section and labels the slides. These were Aussies 
and Kiwis I worked with overseas and that is how they work in some places. BTW, 
they also stand at the bench and put the microtome sideways in order to work 
faster (pull the ribbon off, throw it on the waterbath and go on to the next 
block. Otherwise, forget it, it is not possible and still keep quality and 
sanity intact.

Tim Morken
Supervisor, Histology, IPOX
UCSF Medical Center
San Francisco, CA, USA

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joanne
Sent: Saturday, June 25, 2011 2:50 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] How many tissues an histo tech is suppose to cut per



i've only been working 2 months.  although older, i am new as a histotech 
(graduated in may 2010, found a job in april 2011).  seems management is 
setting a goal of a block per minute as far as cutting goes for me.  i have 
until october to attain this goal. this minute for cutting is to include 
facing, writing out slides, cutting, and putting tray into symphony stainer 
(not to mention getting up to answer the phone, fielding questions regarding 
send-out cases, and other slight cutting interruptions).   this seems an 
extreme, possibly unattainable goal.  i'm up for a challenge  at age 53, but 
any advice would be SWONDERFUL :)

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[Histonet] Re: Histogel

2011-06-27 Thread Robert Richmond
Histogel is indeed expensive, and often not permitted by Management
for that reason.

Preparing your own agar is a bit tricky - you really need a hot plate
and a magnetic stirrer, unlikely items in a histology lab. (2% or 3%
dry agar, in water.)

Back before hospital microbiology turned into the black box it is
today, you used to be able to walk across the hall and pick up a tube
of trypticase soy agar (TSA - I think it was 3% agar with some stuff
in it to make bugs grow) and use that.

One way to use agar is for the pathologist to pour out some melted
agar on a glass slide or metal ruler, and embed small specimens in it
so they stay oriented - works great for temporal artery biopsies and
vasectomy specimens - time consuming.

A blood bank heating block is useful for keeping tubes of agar melted
at the gross desk.

Whether you use Histogel or some other agar, it's very important not
to commit any valuable specimens to it until you're sure it works in
your system. I like to carve out some pseudo-biopsies from a normal
mucosa in a colon resection specimen and run them. - I've seen some
disasters when this precaution wasn't taken.

Bob Richmond
Samurai Pathologist
Knoxville TN

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RE: [Histonet] How many tissues an histo tech is suppose to cut per

2011-06-27 Thread sgoebel
I second this motion!!

Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas  78744
(512)901-0900 ext. 6912


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Blazek,
Linda
Sent: Monday, June 27, 2011 12:10 PM
To: 'Joanne'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] How many tissues an histo tech is suppose to cut
per

Unless you are in some remote area that there aren't any other
facilities around, I would look for a new job!  I don't think your age
should have any bearing on finding one.  If you were close to me I'd
hire you.  Working under that kind of condition is unacceptable in my
opinion.  It promotes errors and that isn't what we are all about.
Those blocks are our patients.

Linda

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joanne
Sent: Saturday, June 25, 2011 2:50 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] How many tissues an histo tech is suppose to cut per


 
i've only been working 2 months.  although older, i am new as a
histotech (graduated in may 2010, found a job in april 2011).  seems
management is setting a goal of a block per minute as far as cutting
goes for me.  i have until october to attain this goal. this minute for
cutting is to include facing, writing out slides, cutting, and putting
tray into symphony stainer (not to mention getting up to answer the
phone, fielding questions regarding send-out cases, and other slight
cutting interruptions).   this seems an extreme, possibly unattainable
goal.  i'm up for a challenge  at age 53, but any advice would be
SWONDERFUL :)   
 
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RE: Re: [Histonet] How many tissues an histo tech is suppose to cutper

2011-06-27 Thread Horn, Hazel V
As a manager I would never expect that kind of turn around.  I think it's 
impossible to achieve.

Hazel Horn
Hazel Horn, HT/HTL (ASCP)
Supervisor of Autopsy/Histology/Transcription
Arkansas Children's Hospital
1 Children's WaySlot 820
Little Rock, AR   72202

phone   501.364.4240
fax501.364.3155

visit us on the web at:www.archildrens.org

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
sgoe...@mirnarx.com
Sent: Monday, June 27, 2011 9:38 AM
To: rjbu...@yahoo.com; histonet-requ...@lists.utsouthwestern.edu; 
histonet@lists.utsouthwestern.edu
Subject: RE: Re: [Histonet] How many tissues an histo tech is suppose to cutper

Another solution...get out of clinical and go into research =)  There are no 
quotas or slide per second expectations in the research world =)  So sorry you 
are having such a bad time with your job.  HT's are not a dime a dozen and 
usually it is fairly easy to find a better job.  Not to mention research pays 
almost double the clinical world!!
Good Luck!!

Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas  78744
(512)901-0900 ext. 6912


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rene J Buesa
Sent: Sunday, June 26, 2011 9:43 AM
To: histonet-requ...@lists.utsouthwestern.edu; histonet@lists.utsouthwestern.edu
Subject: Fw: Re: [Histonet] How many tissues an histo tech is suppose to cutper



---






Joanne:
Read the attachment so you can have an idea about productivity ranges and 
averages in different tasks in the lab.
If you embedded 214 blocks and cut 148  in 5.5 hours, using the averages I 
provided, embedding should have taken 3.5 hours and cutting 6.2 hours which 
means you worked 1.76 times FASTER than the expected average.
René J.

--- On Sat, 6/25/11, Joanne joanne0...@comcast.net wrote:


From: Joanne joanne0...@comcast.net
Subject: [Histonet] How many tissues an histo tech is suppose to cut per
To: histonet@lists.utsouthwestern.edu
Date: Saturday, June 25, 2011, 7:07 PM


i am quite serious in my presentation and request for advice.  i too thought 
this goal was/is ridiculous to expect/ask for from someone so new and to attain 
in 6 months or less.  last monday i embedded 214 blocks and cut 148 between 5am 
and 10:30am (we had almost 600 cassettes to share among 3 people) . . . .for 
someone so very new i thought this pretty good . . . please note: most days 
aren't as hectic.  :)  what is an average though for blocks/minute?  what is 
meant by set sum per block? ---keeping in mind i am new to this field.



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[Histonet] Oncotype

2011-06-27 Thread Amy Self
I was wandering how many of you out there are using oncotype dx. for some of 
your breast patients?  And what is your handling process for this test?


Thanks in advance,
Amy


Amy Self
Georgetown Hospital System

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Re: [Histonet] Oncotype

2011-06-27 Thread Gmail
We do this testing for oncology. They pay for the shipping via fedex.  
The oncologist fills out the requsition and the lab pulls the block ,  
packages it and ships it.


Andrea

On 2011-06-27, at 2:10 PM, Amy Self  
as...@georgetownhospitalsystem.org wrote:


I was wandering how many of you out there are using oncotype dx. for  
some of your breast patients?  And what is your handling process for  
this test?



Thanks in advance,
Amy


Amy Self
Georgetown Hospital System

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Re: [Histonet] Oncotype

2011-06-27 Thread Cohen, Sherene
When I was working in the lab, we sent specimens for Oncotype. They perform. 21 
gene assay to predict the chance of recurrence of the cancer within 10 years. 
You can either send the tissue block or slides (depending on your send out 
policy). The testing can have an impact on the patient's tratment. 

Sherene

- Original Message -
From: histonet-boun...@lists.utsouthwestern.edu 
histonet-boun...@lists.utsouthwestern.edu
To: 'histonet@lists.utsouthwestern.edu' histonet@lists.utsouthwestern.edu
Sent: Mon Jun 27 14:10:59 2011
Subject: [Histonet] Oncotype

I was wandering how many of you out there are using oncotype dx. for some of 
your breast patients?  And what is your handling process for this test?


Thanks in advance,
Amy


Amy Self
Georgetown Hospital System

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Re: [Histonet] How many tissues an histo tech is suppose to cut per

2011-06-27 Thread Patrick Laurie
I have known one or two people who can attain this rate.  However with them,
it is not consistent, especially if there are any interruptions.  I would
take a couple of articles, especially some of Rene Buesa's authoritative
articles to your management and encourage them to set realistic
expectations.  If your manager has any experience in histology, ask them to
show you how to do it, (put them on the spot to try to meet their own
goals).  Good luck.

On Mon, Jun 27, 2011 at 10:51 AM, sgoe...@mirnarx.com wrote:

 I second this motion!!

 Sarah Goebel-Dysart, BA, HT(ASCP)
 Histotechnologist
 Mirna Therapeutics
 2150 Woodward Street
 Suite 100
 Austin, Texas  78744
 (512)901-0900 ext. 6912


 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Blazek,
 Linda
 Sent: Monday, June 27, 2011 12:10 PM
 To: 'Joanne'; histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] How many tissues an histo tech is suppose to cut
  per

 Unless you are in some remote area that there aren't any other
 facilities around, I would look for a new job!  I don't think your age
 should have any bearing on finding one.  If you were close to me I'd
 hire you.  Working under that kind of condition is unacceptable in my
 opinion.  It promotes errors and that isn't what we are all about.
 Those blocks are our patients.

 Linda

 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joanne
 Sent: Saturday, June 25, 2011 2:50 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] How many tissues an histo tech is suppose to cut per



 i've only been working 2 months.  although older, i am new as a
 histotech (graduated in may 2010, found a job in april 2011).  seems
 management is setting a goal of a block per minute as far as cutting
 goes for me.  i have until october to attain this goal. this minute for
 cutting is to include facing, writing out slides, cutting, and putting
 tray into symphony stainer (not to mention getting up to answer the
 phone, fielding questions regarding send-out cases, and other slight
 cutting interruptions).   this seems an extreme, possibly unattainable
 goal.  i'm up for a challenge  at age 53, but any advice would be
 SWONDERFUL :)

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-- 
Patrick Laurie HT(ASCP)QIHC
CellNetix Pathology  Laboratories
1124 Columbia Street, Suite 200
Seattle, WA 98104
plau...@cellnetix.com
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RE: [Histonet] How many tissues an histo tech is suppose to cut per

2011-06-27 Thread CHRISTIE GOWAN

The proper way to do this would be to time each tech in your lab as to how many 
blocks they can cut in one hour. Take everyones number of blocks and do an 
average for your lab. The average for my lab is 2.15 minutes per block. I 
compiled these numbers in an effort to determine what our labor costs are, not 
to set an expectation for productivity. I have some people who cut really fast 
and some who cut slow. I am curious as to how your management came up with 
these numbers and are any of them histotechs??
 Christie

 

 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joanne
 Sent: Saturday, June 25, 2011 2:50 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] How many tissues an histo tech is suppose to cut per
 
 
 
 i've only been working 2 months. although older, i am new as a histotech 
 (graduated in may 2010, found a job in april 2011). seems management is 
 setting a goal of a block per minute as far as cutting goes for me. i have 
 until october to attain this goal. this minute for cutting is to include 
 facing, writing out slides, cutting, and putting tray into symphony stainer 
 (not to mention getting up to answer the phone, fielding questions regarding 
 send-out cases, and other slight cutting interruptions). this seems an 
 extreme, possibly unattainable goal. i'm up for a challenge at age 53, but 
 any advice would be SWONDERFUL :) 
 
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 Histonet@lists.utsouthwestern.edu
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[Histonet] Austin PRN

2011-06-27 Thread sgoebel
Hello all =)

Since I just recently got married and still own a house we do not live
in, I am finding myself in the pickle of 2 houses and not enough
income...Does anyone know of any kind of part time histology jobs in
Austin that I could go to either early until around 7am or late after
5pm?  Or if not histology specific, I could log specimens for intake or
something...I just can't bring myself to ask the question...would you
like fries with that? with a college education and 10 years of
histology experience...I'm doing ok, I just want my fluff back =)

Thanks ya'll!!

 

Sarah Goebel-Dysart, BA, HT(ASCP)

Histotechnologist

Mirna Therapeutics

2150 Woodward Street

Suite 100

Austin, Texas  78744

(512)901-0900 ext. 6912

 

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[Histonet] Invitation to connect on LinkedIn

2011-06-27 Thread Thomas Huynh via LinkedIn
LinkedIn





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[Histonet] Flk2 / Flt3 / CD135 on mouse bone

2011-06-27 Thread Adam .
Hi all,

One of my fellow graduate students is trying to perform immunofluorescence
on PFA fixed, EDTA decalcified mouse bone for Flk2 (aka Flt3 or CD135). So
far, he hasn't had any luck on either paraffin embedded or frozen sections
using HIER. Has anyone done this successfully? I know the ideal way to
perform IF on bone is using a tape-transfer system, but, alas, we don't
quite have that working yet.

Thanks,
Adam
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Re: [Histonet] Flk2 / Flt3 / CD135 on mouse bone

2011-06-27 Thread koellingr


Adam/his fellow grad student, 

  

I could be somewhat off not being up to date with current literature.  Sorry.  
But used to look for Flk2/Flt3/CD135 in murine bone marrow and not the bone 
itself.  In immature hematopoeitic progenitor cells.  Along with looking in 
thymus, etc.  But for something like femurs, I removed the bone marrow, and 
there are some slick ways to do it without disrupting the core architecture too 
much.  Could take it out and obviously flow (cytometry) the cells.  But could 
also get out a fairly intact core and freeze it, or paraffin process/section it 
or glycol methacrylate section it and worry very little about the minute amount 
of trabecular bone in murine bone marrow. Depending on age, etc of course. 

  

So unless for the specific needs of the project call for looking actually for 
staining within the cortical bone, I'd take that problem out of the picture by 
getting the bone marrow out and then not having to worry  about decalcification 
and tape transfer and things like that.  Makes IHC staining a lot easier in my 
experience but  perhaps there are those out there who have worked out whole, 
intact mouse bone CD135 staining. 



Ray 



Ray Koelling 

PhenoPath Labs 

Seattle WA 



- Original Message -




From: Adam . anonwu...@gmail.com 
To: histonet@lists.utsouthwestern.edu 
Sent: Monday, June 27, 2011 5:49:23 PM 
Subject: [Histonet] Flk2 / Flt3 / CD135 on mouse bone 

Hi all, 

One of my fellow graduate students is trying to perform immunofluorescence 
on PFA fixed, EDTA decalcified mouse bone for Flk2 (aka Flt3 or CD135). So 
far, he hasn't had any luck on either paraffin embedded or frozen sections 
using HIER. Has anyone done this successfully? I know the ideal way to 
perform IF on bone is using a tape-transfer system, but, alas, we don't 
quite have that working yet. 

Thanks, 
Adam 
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Re: [Histonet] Flk2 / Flt3 / CD135 on mouse bone

2011-06-27 Thread Adam .
Hi Ray,

That is a great idea. We are indeed looking for Flk2 expression on
hematopoietic progenitors cells, but alas, we are looking at these cells in
relationship to bone elements such as osteoblasts, so we need to do it on
intact bone.

Adam

On Mon, Jun 27, 2011 at 8:43 PM, koelli...@comcast.net wrote:

 Adam/his fellow grad student,



 I could be somewhat off not being up to date with current literature.
 Sorry.  But used to look for Flk2/Flt3/CD135 in murine bone marrow and not
 the bone itself.  In immature hematopoeitic progenitor cells.  Along with
 looking in thymus, etc.  But for something like femurs, I *removed* the
 bone marrow, and there are some slick ways to do it without disrupting the
 core architecture too much.  Could take it out and obviously flow
 (cytometry) the cells.  But could also get out a fairly intact core and
 freeze it, or paraffin process/section it or glycol methacrylate section it
 and worry very little about the minute amount of trabecular bone in murine
 bone marrow. Depending on age, etc of course.



 So unless for the specific needs of the project call for looking actually
 for staining within the cortical bone, I'd take that problem out of the
 picture by getting the bone marrow out and then not having to worry  about
 decalcification and tape transfer and things like that.  Makes IHC staining
 a lot easier in my experience but  perhaps there are those out there who
 have worked out whole, intact mouse bone CD135 staining.



 Ray



 Ray Koelling

 PhenoPath Labs

 Seattle WA

  --

 *From: *Adam . anonwu...@gmail.com
 *To: *histonet@lists.utsouthwestern.edu
 *Sent: *Monday, June 27, 2011 5:49:23 PM
 *Subject: *[Histonet] Flk2 / Flt3 / CD135 on mouse bone


 Hi all,

 One of my fellow graduate students is trying to perform immunofluorescence
 on PFA fixed, EDTA decalcified mouse bone for Flk2 (aka Flt3 or CD135). So
 far, he hasn't had any luck on either paraffin embedded or frozen sections
 using HIER. Has anyone done this successfully? I know the ideal way to
 perform IF on bone is using a tape-transfer system, but, alas, we don't
 quite have that working yet.

 Thanks,
 Adam
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