[Histonet] Water contamination [Scanned]
Kemlo Rogerson
Kemlo.Rogerson <@t> elht.nhs.uk
Tue Nov 30 02:34:41 CST 2004
I don't think fiddling with a few percentages of alcohol in the initial
steps of dehydration makes any difference, bung it straight in 100%, it'll
get diluted after a few batches.
Change your last alcohol more regularly or have a 'drip bottle' of alcohol
and, if you are manual staining, give the slides a quick wash of fresh
alcohol before entering the first xylene. That's a point, did you say you
were manual staining or not?
Kemlo Rogerson
Cellular Pathology Manager
East Lancashire Hospitals NHS Trust
DD. 01254-294162
Mobile 0774-9754194
-----Original Message-----
From: Jose Luis Palazon Fernandez [mailto:jluis.palazon <@t> icman.csic.es]
Sent: 29 November 2004 16:59
To: histonet <@t> lists.utsouthwestern.edu
Subject: Re: [Histonet] Water contamination [Scanned]
In my lab we normally use 95 % EtOH before absolute alcohols, instead of the
70 % you use, without any problem. Maybe your contaminating agent is 70 %
EtOH, try changing this step with a 95 % one
José Luis
El dia 27/11/2004 19:32 usted envio el siguiente mensaje:
>Date: 27 de Noviembre de 2004 19:32:07
>From: Paula Pierce <contact <@t> excaliburpathology.com>
>Subject: [Histonet] Water contamination
>To: histonet <@t> lists.utsouthwestern.edu
>
> First, you SLICE meat. Histotechs SECTION tissue.
>
> 70% EtOH is 30% water. You are probably getting too much water carryover
into your 100%. Make sure the 100% EtOH is 100%. If the solutions are fresh,
10 to 20 dips each is enough time for dehydration before xylene and
coverslipping.
>
>
> Paula Pierce, HTL(ASCP)HT
>
> Excalibur Pathology, Inc.
> 631 N. Broadway
> Moore, OK 73160
> 405-759-3953
> contact <@t> excaliburpathology.com
> www.excaliburpathology.com
> _______________________________________________
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>
Universidad de Oriente-Isla Margarita-Venezuela
actualmente en: Instituto de Ciencias Marinas de Andalucia
Puerto Real, Cádiz, España.
email: jluis.palazon <@t> icman.csic.es
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