CONFOCALMICROSCOPY Archives

October 2009

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:
Claire Brown <[log in to unmask]>
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Thu, 1 Oct 2009 10:58:39 -0500
Content-Type:
text/plain
Parts/Attachments:
text/plain (6 lines)
Another thing you can do is put subresolution (0.1 um) beads on one of your
samples - i.e. on top of the cells. Then make sure they are deconvolved
properly along with your sample fluorescence.

Claire

ATOM RSS1 RSS2