RE: bone marrow trephines
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From: | "Weems, Joyce" <JWEEMS@sjha.org> (by way of histonet) |
To: | histonet <histonet@magicnet.net> |
Reply-To: | |
Content-Type: | text/plain; charset="us-ascii" |
We "demineralize" this way also, and have and alk phos immuno procedure
works better on our bone marrows. J:>)
>----------
>From: Hagerty, Marjorie A.[SMTP:mhagerty@emc.org]
>Sent: Thursday, November 12, 1998 2:58 PM
>To: Histonet
>Subject: bone marrow trephines
>
>
>Histonetters,
>We are currently using RDO for one hour to decal our BM core bxs. This works
>perfectly for us, they are easy to cut, and the nuclear detail is excellent.
>I think, however, that the HCL in the decalcifier may be interfering with
>our Kappy/Lambda immunoperoxidase staining. I tried an antigen retrieval
>solution specifically for decalcified tissue but that did not seem to
>correct the problem. Doing this on one case does not count as any kind of
>"study" so this may be an excellent product. We would like to try a non-HCL
>decalcifier. Alex metioned formal citrate but our clinicians would not
>tolerate the length of time it takes. Does anyone know of a decalcifier that
>takes no more than an hour for very small core bxs and does not use HCL?
>Thanks
>Marg
>EMC, Rancho Mirage, CA
>
>
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