[Histonet] Protocol of MMA Plastic section TRAP staining

2014-10-22 Thread Dorothy Hu
Dear Histoneters,

Can someone email me your TRAP protocol for MMA section? I have one, but
staining is not consistent. No matter I stain for how long, ~ several hours
sometimes. There are always variations. I sincerely hope I can get
different protocol form you and make change. I remember saw other TRAP
protocol which is much longer than mine.

The protocol I used was:

1. Dissolve 12mg Naphthol AS-MX phosphate (Sigma, N-5000) in 0.5ml N,N
methylformamide (Sigma,D8654).
2. Mix above into 50 ml Sodium tartrate with 0.1M sodium acetate buffer at
pH5.0.
3. Mix 30mg Fast Red Violet LB salt (Sigma, F3381) with above solution and
filter.

Stain slides @37oC for at least one hour. The solution can be use for one
month when stored in 4oC.
Continue to do counterstain and mount slides.
Thank you.

Dorothy Hu
MGH Endocrine histocore
Email: d...@partners.org
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Re: [Histonet] Protocol of MMA Plastic section TRAP staining

2014-10-22 Thread Jack Ratliff
Hello Dorothy! I will forward you my protocol just as soon as I can get to my 
computer.

On a side note, I no longer Chair the Hard Tissue Committee for the National 
Society for Histotechnology (NSH) as I have now been elected to the NSH Board 
of Directors as the Region III Director for the Southeast region. With that 
said, Sarah Mack is now the new Hard Tissue Committee Chairperson and Kim 
Simmons is the Education Development Manager for the NSH. I tell you this 
because Sarah is located in your part of the country and is currently the 
Histology Core Manager at University of Rochester Medical Center, Center for 
Musculosketeal Research. She works with bone and will be an good resource for 
you. I have copied her on this message. Kim Simmons will be helping to organize 
bone related educational materials and events for the NSH in the next year so 
she will be another good reference for you to follow. I have copied her to this 
message as well. I will still be a part of the Hard Tissue Committee in a 
supporting role. I just wanted you to know your additional options for 
information related to the histology of bone, biomaterials and medical device 
implants.

Best Regards,

Jack Ratliff






 On Oct 22, 2014, at 3:20 PM, Dorothy Hu abt...@gmail.com wrote:
 
 Dear Histoneters,
 
 Can someone email me your TRAP protocol for MMA section? I have one, but
 staining is not consistent. No matter I stain for how long, ~ several hours
 sometimes. There are always variations. I sincerely hope I can get
 different protocol form you and make change. I remember saw other TRAP
 protocol which is much longer than mine.
 
 The protocol I used was:
 
 1. Dissolve 12mg Naphthol AS-MX phosphate (Sigma, N-5000) in 0.5ml N,N
 methylformamide (Sigma,D8654).
 2. Mix above into 50 ml Sodium tartrate with 0.1M sodium acetate buffer at
 pH5.0.
 3. Mix 30mg Fast Red Violet LB salt (Sigma, F3381) with above solution and
 filter.
 
 Stain slides @37oC for at least one hour. The solution can be use for one
 month when stored in 4oC.
 Continue to do counterstain and mount slides.
 Thank you.
 
 Dorothy Hu
 MGH Endocrine histocore
 Email: d...@partners.org
 ___
 Histonet mailing list
 Histonet@lists.utsouthwestern.edu
 http://lists.utsouthwestern.edu/mailman/listinfo/histonet
 

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