SPAM-LOW: [Histonet] Partially muddy slides
pruegg <@t> ihctech.net
Sun Nov 21 12:43:15 CST 2010
Sounds to me like an individual tissue collection issue (aka time to
fixative) since it is so random and individual. Ask those collecting the
samples to record when the sample was removed from the body, and when it
went into fixative if you can get them to do that.
Patsy Ruegg, HT(ASCP)QIHC
12635 Montview Blvd. Ste.215
Aurora, CO 80045
From: histonet-bounces <@t> lists.utsouthwestern.edu
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histotech <@t> imagesbyhopper.com
Sent: Tuesday, November 16, 2010 10:09 AM
To: histonet <@t> lists.utsouthwestern.edu
Subject: SPAM-LOW: [Histonet] Partially muddy slides
We are having an issue in our lab with some inconsistent staining. It's an
odd situation. One small biopsy can stain reasonably well over most of the
tissue, but then one area of it is muddy. This does not affect all the
slides in the same staining rack, nor does it affect all the small biopsies
that were processed in the same processing cycle. Troubleshooting this has
been difficult, at best. It's sort of hit or miss on when/where the
Here are my thoughts:
** I don't know if this is a processing issue, a staining issue or perhaps
even a collection issue.
** If it affected all small biopsies equally, I would be tempted to question
the processing/fixation. But it doesn't affect across the board.
** If all the staining was muddy, I would look to the stainer, but again,
even within the same slide, we can have clear and muddy areas.
** The stainer is a Leica XL (about 3 years old), hooked up to tap water
for the washes.
** We are using a regressive staining method with Fisher brand Protocol
Harris hematoxylin and Protocol Eosin Y. We use acid alcohol and ammonia
water for differentiating and bluing.
** The xylene we use is recycled, but verified for purity.
** The alcohols are recycled, but the last alcohol prior to the
xylene/coverslipping is "pure", not recycled (for just in case).
Suggestions on what could be causing this issue would be greatly
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