[Histonet] Anti-Human Hepatocyte antibody clone OCH1E5

2013-07-12 Thread Randolph-Habecker, Julie
Hey Histonetters,

Has anyone noted negative staining with the anti-human hepatocyte antibody 
Clone OCH1E5 on hepatocytes surrounding the centrilobular vein? We are staining 
mouse liver samples and get great staining on about 80-90% of the hepatocytes 
in normal liver but then see very low to frank negative staining only in this 
region.

Thanks!

Julie

Julie Randolph-Habecker, Ph.D.
Director, Experimental Histopathology Shared Resources
Fred Hutchinson Cancer Research Center
1100 Fairview Ave N, DE-360
Seattle WA 98109-1024
Tel: 206-667-6119
Fax: 206-667-6845
jhabe...@fhcrc.org

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[Histonet] Luciferase IHC!

2011-11-02 Thread Randolph-Habecker, Julie
Thanks for the help!
We actually tried antigen retrieval in Holy water in a pressure cooker for 10 
minutes. I even brought in an old priest and a young priest to perform the 
staining but no luck! Sorry, no vendor for the holy water - the old priest 
makes his own.

I enjoyed the laugh! This project has been hell!

Thanks,

Julie

Message: 21
Date: Wed, 2 Nov 2011 08:46:28 -0500
From: Beckham, Sharon s...@stowers.org
Subject: RE: [Histonet] Luciferase IHC
To: 'O'Donnell, Bill' billodonn...@catholichealth.net, Kim Donadio
one_angel_sec...@yahoo.com, Randolph-Habecker, Julie
jhabe...@fhcrc.org, histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Message-ID:

2c40e43d1f7a56408c4463fd245dddf98aee2...@exchmb-02.stowers-institute.org

Content-Type: text/plain; charset=iso-8859-1

You know sometimes I wish these emails had a LIKE button on them.   I found 
this quite funny and wanted to LIKE it.  Too much facebook for me! 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of O'Donnell, Bill
Sent: Wednesday, November 02, 2011 8:19 AM
To: Kim Donadio; Randolph-Habecker, Julie; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Luciferase IHC

Actually, I have found that holy water reduces its sensitivity, greatly 
diminishes its signal and will destroy its reactivity. (Listen closely and you 
will hear the slide scream and growl and tell you no one likes you) (It's only 
Wednesday, what'll Friday look like?)

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Kim Donadio
Sent: Tuesday, November 01, 2011 7:01 PM
To: Randolph-Habecker, Julie; histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Luciferase IHC

You have to soak it in holy water, then all H311 will break out
 
Sorry, I couldnt resist. 
 
 



From: Randolph-Habecker, Julie jhabe...@fhcrc.org
To: histonet@lists.utsouthwestern.edu
Sent: Tuesday, November 1, 2011 6:49 PM
Subject: [Histonet] Luciferase IHC

Has anyone had good results staining for luciferase in FFPE tissue? If so, what 
antibody did you use.



Thanks!!



Julie



Julie Randolph-Habecker, Ph.D.

Director, Experimental Histopathology Shared Resources

Fred Hutchinson Cancer Research Center

1100 Fairview Ave N, DE-360

Seattle WA 98109-1024

Tel: 206-667-6119

Fax: 206-667-6845

jhabe...@fhcrc.org



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End of Histonet Digest, Vol 96, Issue 3
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[Histonet] Luciferase IHC

2011-11-01 Thread Randolph-Habecker, Julie
Has anyone had good results staining for luciferase in FFPE tissue? If
so, what antibody did you use.

 

Thanks!!

 

Julie

 

Julie Randolph-Habecker, Ph.D.

Director, Experimental Histopathology Shared Resources

Fred Hutchinson Cancer Research Center

1100 Fairview Ave N, DE-360

Seattle WA 98109-1024

Tel: 206-667-6119

Fax: 206-667-6845

jhabe...@fhcrc.org

 

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[Histonet] Turnaround time for Research Pathology

2010-08-05 Thread Randolph-Habecker, Julie
Folks,

 

I am looking for some standard turnaround times for histology services
including processing to embedding, processing to HE, and processing to
HE and IHC. Does anyone have that data?

 

Also, how do other folks handle standard turnaround time for research
samples? We may get anything from 5 specimens to 300 specimens that just
need paraffin processing and 1 HE. Or we may get a request for 10
samples for paraffin-processing, 10 slides each with 2 HE and 7
different IHC stains per case.

 

Any insight on this would be very helpful.

 

Thanks,

 

Julie

 

Julie Randolph-Habecker, Ph.D.

Director, Experimental Histopathology Shared Resources

Fred Hutchinson Cancer Research Center

1100 Fairview Ave N, DE-360

Seattle WA 98109-1024

Tel: 206-667-6119

Fax: 206-667-6845

jhabe...@fhcrc.org

 

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[Histonet] Control slides for Flag-Tag IHC

2010-02-25 Thread Randolph-Habecker, Julie
Folks,

I am looking for a control for some Flag-tag IHC I am doing on FFPE
tissue. I was wondering if someone could share some slides off of a
block of flag transfected cells.

THANKS!!

Julie

Julie Randolph-Habecker, Ph.D.
Staff Scientist - Director
Experimental Histopathology Shared Resource
Fred Hutchinson Cancer Research Center
1100 Fairview Ave, N. DE-360 (Please note new location)
Seattle WA 98109-1024
206-667-6119
jhabe...@fhcrc.org

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[Histonet] CD4 and CD8 in FFPE mouse tissue

2009-08-24 Thread Randolph-Habecker, Julie
Folks,

It's my annual inquiry as to whether someone has optimized
immunohistochemistry for CD4 and CD8 on formalin-fixed paraffin mouse
tissue. Over the years we have tried lots of different antibodies but I
am wondering if there is anything new that we have not tried. Any leads
would be great!

Thanks,

Julie

Julie Randolph-Habecker, Ph.D.
Staff Scientist - Director
Experimental Histopathology Shared Resource
Fred Hutchinson Cancer Research Center
1100 Fairview Ave, N. DE-360 (Please note new location)
Seattle WA 98109-1024
206-667-6119
jhabe...@fhcrc.org

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[Histonet] Problems with mouse brains

2009-04-03 Thread Randolph-Habecker, Julie
Folks,

I need some input on a problem we're seeing with some mouse brain
samples. The samples are from new born mice P0 to P14 which have been
fixed in 10% NBF (Fisher brand and well within expiration date) for 72
hours. They are then transferred to 70% etoh and processed on an 8 hour
process. After the tissue is embedded, we are taking sagital sections,
drying them overnight, and then baking overnight at 60C. They are then
stained with HE. This has been working great but now all of a sudden we
have very light HE staining, nuclear bubbling, and extensive tissue
cracking. I also have noticed some formalin pigment.

My first thought is that there was difference in formalin or time in
formalin but that is not the case. I also wondered if the tissue might
be exposed to excessive heat. We checked all of the temperatures in our
processor, embedding center, and water baths - all were within
tolerance. 

Any ideas what might cause all three artifacts? Could it be from
inadequate paraffin infiltration?

Any help would be greatly appreciated! 

Thanks,

Julie

Julie Randolph-Habecker, Ph.D.
Staff Scientist - Director
Experimental Histopathology Shared Resource
Fred Hutchinson Cancer Research Center
1100 Fairview Ave, N. DE-360 (Please note new location)
Seattle WA 98109-1024
206-667-6119
jhabe...@fhcrc.org

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