anyone using AGAR to processes specimens?

From:	Susie Seward <sseward@statlab.com> (by way of histonet)
To:	histonet@histosearch.com
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I know someone who is experiencing problems when they change their Paraplast
(using Paraplast plus with DMSO) on their processor. The very next day after
changing the paraffin, the agar and tissue is "brittle" "shrunken"
"disintegrated" but the next day and rest of the month it is fine. What may
be
causing this?

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