[Histonet] collagen I IHC detection in mouse pulmonary fibrosis

2013-07-07 Thread abijag
All,

I would like to quantify collagen 1 in bleomycin induced lung fibrosis in mice. 
It will be highly appreciated if any of our histonetters will share their 
protocol for IHC staining of perfusion fixed(10% NBF) mouse fibrotic lungs.



Thanks in advance



Abi
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


Re: [Histonet] phobic slides

2013-07-07 Thread Tony Reilly
Hi Bruce
 
Our Immuno staff have reported the uneven staining artifact with some brands of 
coated slides but not others and we are staining on the Ventana platform.  I 
have also noticed in some cases when slides are inadequately dewaxed the 
Haematoxylin will stain even though there is loss of immunostaining..
 
regards
Tony
 
 
 

Tony Reilly  B.App.Sc. , M.Sc.
Chief Scientist, Anatomical Pathology
Pathology Queensland-PA Laboratory 

Health Services Support Agency | Department of Health
 
Level 1, Building 15,Princess Alexandra Hospital
Ipswich Road,WOOLLOONGABBA  Qld4102
Ph: 07 3176 2412
Mob: 0402 139411
Fax: 07 3176 2930
Email: tony_rei...@health.qld.gov.au
Web:  www.health.qld.gov.au/qhcss/
 
 


 Bruce Gapinski bgapin...@pathgroup.com 7/6/2013 2:57 am 
Histonians!
Has anyone else had incorrect  IHC  staining due to overly 
charged slides that are hydrophobic? My Ventana service department was out 
because I kept complaining about incomplete staining. For instance, the control 
at the top of the slide stained with  both DAB and hematoxylin. But on the very 
same slide the hematoxylin was missing from the patient tissue.
I told them how this unnerved me. If the same thing happens but 
the hematoxylin stains and the DAB does not...I could be looking at a false 
negative. This may have happened already as far as I know.
The solution according to Ventana is to take 4 slides from each 
new box of slides (1/2 gross) and do a vortex mix on each of them one at a 
time. Then you know you have valid slides to stain patient tissues! I have no 
time for this. And I'm trying to believe it but it's just not scientific. How 
is it that my results have been free of this phobia for over a year? Why 
didn't I get this (EVER) with Dako instrumentation? The answer, I was told, was 
that the humidity was a problem. If I were to take this to it's ridiculous 
conclusion, I would need to inform oncologists not to operate during these 
incorrectly humidified days. It IS summer so I'm not sure how much humidity is 
required.

1.   What brand of slides do you use?

2.   Have you had the slide phobia so that it compromised the results? 
(Slide-phobia is for retired Histologists, no?)

3.   (I think I know the answer but I just have to ask) Do you validate 
slides?

Bruce Gapinsk HT (ASCP)
Chief Histologist
Marin Medical Laboratories
PathGroup SF




Important Notice: This e-mail is intended for the use of the person to whom it 
is addressed and may contain information that is privileged and confidential. 
If you are not the intended recipient, any disclosure, copying, distribution, 
or use of the contents of this message is strictly prohibited. If you have 
received this e-mail in error, please destroy this message and contact the 
Security Officer at PathGroup, Inc immediately at 615-562-9255. Thank you
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu 
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


This email, including any attachments sent with it, is confidential and for the 
sole use of the intended recipient(s). This confidentiality is not waived or 
lost, if you receive it and you are not the intended recipient(s), or if it is 
transmitted/received in error.
Any unauthorised use, alteration, disclosure, distribution or review of this 
email is strictly prohibited.  The information contained in this email, 
including any attachment sent with it, may be subject to a statutory duty of 
confidentiality if it relates to health service matters.
If you are not the intended recipient(s), or if you have received this email in 
error, you are asked to immediately notify the sender by telephone collect on 
Australia +61 1800 198 175 or by return email.  You should also delete this 
email, and any copies, from your computer system network and destroy any hard 
copies produced.
If not an intended recipient of this email, you must not copy, distribute or 
take any action(s) that relies on it; any form of disclosure, modification, 
distribution and/or publication of this email is also prohibited.
Although Queensland Health takes all reasonable steps to ensure this email does 
not contain malicious software, Queensland Health does not accept 
responsibility for the consequences if any person's computer inadvertently 
suffers any disruption to services, loss of information, harm or is infected 
with a virus, other malicious computer programme or code that may occur as a 
consequence of receiving this email.
Unless stated otherwise, this email represents only the views of the sender and 
not the views of the Queensland Government.
**


[Histonet] Calcein labeled plastic section mounting procedure

2013-07-07 Thread Dorothy Hu
Hi All,

I am relatively new to plastic embedding media. I need to permanently mount
acrylosin calcein labeled undecaled bone sections under coverslip. Would be
possible for someone tell me that do I need to de-plastic first in xylene?
What mounting media should I use to protect fluorescent green color fading?

Much gratitude.

Dorothy Hu
abt...@gmail.com
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet