CONFOCALMICROSCOPY Archives

December 2004

CONFOCALMICROSCOPY@LISTS.UMN.EDU

Options: Use Monospaced Font
Show Text Part by Default
Show All Mail Headers

Message: [<< First] [< Prev] [Next >] [Last >>]
Topic: [<< First] [< Prev] [Next >] [Last >>]
Author: [<< First] [< Prev] [Next >] [Last >>]

Print Reply
Subject:
From:
Michael Cammer <[log in to unmask]>
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Wed, 15 Dec 2004 15:42:08 -0500
Content-Type:
TEXT/PLAIN
Parts/Attachments:
TEXT/PLAIN (14 lines)
Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

I would add incubation with trypsin and/or pepsin to remove all residual
proteins and a strong detergent.
We may have to begin reusing the special Olympus TIRF coverslips.  One
idea we have (but havene't tried yet) is commercial laundry detergents
which are enzyme detergent cocktails.
 -Michael

> too much of a problem. The hard parts are washing to the point of
> scrupulous cleanliness and sterilizing. One approach would be to wash
> the culture vessels with soap/water, rinse well, soak in 70% ethanol and

ATOM RSS1 RSS2