CONFOCALMICROSCOPY Archives

September 2006

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:
Thomas Stroh <[log in to unmask]>
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Fri, 15 Sep 2006 12:36:06 -0400
Content-Type:
text/plain
Parts/Attachments:
text/plain (29 lines)
Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

Dear All

I have the following problem:  We want to quantify abundant approx.1 µm  
bodies in confocal stacks.  The user is oversampling by acquiring 0.1µm  
step size z-stacks through a 100x/1.4 N.A lens on a LSM 510.  However, it  
still appears difficult to be confident  in our interpretation whether a  
given object is continuous or not in neighboring sections due to  
limitations in resolution.  Can we improve our confidence in determining  
the size and number of bodies using deconvolution of these images?  If so,  
what software would be recommended?





-- 
Thomas Stroh, Ph.D.
Director, MNI Microscopy Unit
Montreal Neurological Institute
McGill University
3801 University Street, Room 753a
Montreal, PQ, H3A 2B4, CANADA
Phone: (514) 398-2719, Fax: (514) 398-5871

Using M2, Opera's revolutionary e-mail client: http://www.opera.com/m2/

ATOM RSS1 RSS2