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April 2002

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From:
Martin Wessendorf <[log in to unmask]>
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Tue, 2 Apr 2002 10:13:06 -0600
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Hey, folks--

We have a BioRad 1024 running LaserSharp 3.2 on an OS/2 machine.  I've
recently tried to set up a "method" for imaging triple-labeled tissue
using photon-counting.  I began by opening the default "triple-labeling"
method, going to "setup", pulling down to "method" and choosing
"save-as".

After that, I simply opened my new method and repeated the steps,
chosing "edit method", instead.  When editing it, I expected that all
I'd need to do was to select the "mixer" button, choose photon-counting
("PhC" rather than "PMT"), and turn on the correct PMT for each mixer.
I did so, and was able to collect single images for each color.

However, the real trouble began when I attempted to collect a sequential
z-series.  This is something we did all the time using the default
"triple-labeling" method, and so I was expecting no changes.  The method
would appear to set everything up correctly, but when it came time to
collect the images, only one color would be imaged--for the other two it
would be as if the PMT was turned off: the image-stacks would be saved,
but would be empty, with every pixel at a value of zero.  The color that
is successfully saved varies from occasion to occasion, which makes
things particularly confusing!

So...does anyone out there have any insight into what's going wrong?
Has anyone successfully made a method-file for photon-counting that
works?

Thanks!

Martin Wessendorf
--
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]

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