Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

There is also a "Synch Windows" option available that will write the
same ROI into several selectable windows.  It should be available on
the plugins page at the IJ web site.



Date sent:              Mon, 13 Jun 2005 11:57:27 +0630
Send reply to:          Confocal Microscopy List <[log in to unmask]>
From:                   Nandini Rangaraj <[log in to unmask]>
Subject:                IMAGE J
To:                     [log in to unmask]

> Search the CONFOCAL archive at
> http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
>
> Hi ,
> Does anybody know how to quantitate fluorescence in a dual image (ie
> getting fluorescencs values for FITC and Texasred separately) using
> the same ROI(region of interest) using IMAGE J? Thanks in advance
> Nandini
>

Joel B. Sheffield, Ph.D
Department of Biology
Temple University
Philadelphia, PA 19122
Voice: 215 204 8839
e-mail: [log in to unmask]