RE: fixatives
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From: | jim <jim@proscitech.com.au> |
To: | "'Berger, Jennifer'" <jberger@lrri.org>, "'histonet'" <histonet@Pathology.swmed.edu> |
Reply-To: | |
Date: | Tue, 13 Jul 1999 15:27:28 +1000 |
Content-Type: | text/plain; charset="us-ascii" |
Hi Jennifer -
For EM purposes its not a good idea to store in fixative for any lengths of
time. GA keeps on cross-linking which affects structure at very high powers.
How long is an endless question; many procedures have somewhat arbitrary timing
schedules suggested, these can be modified but taken to extreme the result will
be poor. Storage in buffer is better than in GA, but slowly some of the lipids
will be lost.
Don't store in fixative. Store in buffer or low alcohol for not much over a
week. Then process and embed and cure.
Cheers
Jim Darley
ProSciTech Microscopy PLUS
PO Box 111, Thuringowa QLD 4817 Australia
Ph +61 7 4774 0370 Fax:+61 7 4789 2313 service@proscitech.com.au
Great microscopy catalogue, 500 Links, MSDS, User Notes
www.proscitech.com.au
On Tuesday, July 13, 1999 1:09 AM, Berger, Jennifer [SMTP:jberger@lrri.org]
wrote:
> We are going to be embedding rat lung tissue in GMA . How long can you store
> the tissue in a fixative of paraformaldehyde 1% gluteraldehyde in a
> phosphate buffer?
> Thanks
> Jennifer
>
> Jennifer Berger
> Lovelace Respiratory Research Institute
> Albuquerque, NM
> jberger@lrri.org
>
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