We get our B-plus from BBC Biomedical.
Charlene
-----Original Message-----
From: histonet-bounces@lists.utsouthwestern.edu [mailto:histonet-bounces@lists.utsouthwestern.edu] On Behalf Of Weber, Susan (VHACLE)
Sent: Wednesday, May 07, 2008 12:10 PM
To: Paul Bradbury; karen adams; HistoNet Server
Subject: RE: [Histonet] B-plus question. .
I may have missed this, but may I have the name of the Vendor you purchase your B-plus from. Thanks.
Susan M Weber HT(ASCP)
Histology Supervisor
Louis Stokes Cleveland VA Medical Center
10701 East Blvd
Cleveland, Ohio 44106
(216) 791-3800 X6154
-----Original Message-----
From: histonet-bounces@lists.utsouthwestern.edu
[mailto:histonet-bounces@lists.utsouthwestern.edu] On Behalf Of Paul Bradbury
Sent: Tuesday, May 06, 2008 9:53 AM
To: karen adams; HistoNet Server
Subject: Re: [Histonet] B-plus question
Hi Karen,
I have been using the same sequence of reagents for several years with great success. We routinely fix bone marrow cores for 3 hours in B-plus,
rinse in water, decalcify, rinse again, and put the cassette in with all
the other tissues for processing. B-plus contains formaldehyde anyway, so your are not introducing a different reagent when you transfer them to formalin during processing.
B-plus gives much better cytological detail than formalin. Nuclear detail is crisper, granules are better preserved, hemosiderin is not effected. CD-3, CD-20, kappa and lambda, etc. all work beautifully after
B-plus. It also has the advantage of not producing an fixation artefact pigment like B-5 does. I think you will be happy with your decision to change.
Paul Bradbury
Kamloops, Canada
karen adams wrote:
> Hello all....we are changing bone marrow fixative from formalin to
B-plus.
> If we fix for the required time in B-plu and then process on the VIP
w/ the
> other specimens using formalin are there any effects on the tissue
going
> from B-plus to formalin??
> Thank you in advance
>
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