CONFOCALMICROSCOPY Archives

April 2011

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:
Martin Wessendorf <[log in to unmask]>
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Thu, 14 Apr 2011 15:41:58 -0500
Content-Type:
text/plain
Parts/Attachments:
text/plain (28 lines)
*****
To join, leave or search the confocal microscopy listserv, go to:
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy
*****

On 4/14/2011 3:31 PM, Mark Cannell wrote:

> I'm afraid the idea is MUCH older than 2008. I recall reading a paper
> from the (?) 1960's that discussed the idea that the diffraction limit
> was not a real limit at all. I believe they were using bacteria as an
> example of where knowledge of the object imparts more information to
> overcome the 'limit'

I think no one would deny that if you know what you're looking at, you 
can break the "resolution barrier"--STORM and PALM being prime examples. 
  However, I'd still be interested in hearing whether--without having 
any additional information about the sample--there is any theoretical 
limit to resolution in fluorescence microscopy, other than that imposed 
by signal-to-noise ratio.

Martin
-- 
Martin Wessendorf, Ph.D.                   office: (612) 626-0145
Assoc Prof, Dept Neuroscience                 lab: (612) 624-2991
University of Minnesota             Preferred FAX: (612) 624-8118
6-145 Jackson Hall, 321 Church St. SE    Dept Fax: (612) 626-5009
Minneapolis, MN  55455                    e-mail: [log in to unmask]

ATOM RSS1 RSS2