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

Or you might try ImageJ from:

http://rsb.info.nih.gov/ij/

On May 16, 2006, at 3:32 PM, Peng Xi wrote:

> Search the CONFOCAL archive at
> http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
>
> Hi,
>      You might have experienced the power of Confocal Assistant. Now, 
> when you have a set of images which is NOT Bio-Rad PIC format, what 
> can you do to use Confocal Assistant? I searched hard and found that 
> there is no simple answer. In this website Lance Ladic gave a solution 
> to this (http://www.biotech.ufl.edu/EM/data/tiff.html), but it is 
> difficult to put into practice. So, I compiled this small program to 
> answer this question. You can find it from:
> http://www.cyto.purdue.edu/flowcyt/software/picc1.htm
>     Thank you.
>
> -- 
>
> Sincerely,
> Peng Xi
> Purdue University Cytometry Laboratories
> Bindley Bioscience Center
> 1203 W. State Street
> West Lafayette, IN 47907
> Tel: 765-494-0757
> Fax: 765-494-0517
> http://web.ics.purdue.edu/~pxi
>
>

Michael J. Herron,  U of MN, Dept. of Entomology
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