Subject: | |
From: | |
Reply To: | |
Date: | Mon, 27 Jun 2011 13:49:29 -0500 |
Content-Type: | text/plain |
Parts/Attachments: |
|
|
*****
To join, leave or search the confocal microscopy listserv, go to:
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy
*****
Hallo,
thanks everybody for their input regarding this topic.
I have some results from a simple test.
Long dwell time (200 us) seem to produce essentially the same signal to
background ratio as accumulation of 100 images with 2us dwell times:
signal:
1 x 200us dwell time:
area (pixels) mean STDEV signal-to-background
specimen 20812 181.76 34.44 14.63
background 20812 12.42 8.99
100 x 2 us dwell time, Sum of frames
area (pixels) mean STDEV signal-to-background
specimen 20812 185.28 33.97 14.73
background 20812 12.58 8.97
The specimen is a Chroma fluorescent slide occupying half of the field of view,
the other half does not have any sample (= background).
The Sum was calculated in ImageJ (Image-Stack-Z Project-Sum of Slices).
FYI,
I also tested for the linearity of the signal versus laser power in the photon
counring mode to see when the pile-up error would become noticeable.
Using 10 us dwell time, spectral detector was set to narrow width (2 nm band
pass)to restrict the photon flux. The signal seems to scale well with intensity,
with just a slight drop off at the highest laser powers (but some of that drop
off can be due to photobleahching; after acquisition I zoomed out and the
scanned area showed as a darker rectangle):
(results from an area of 16756 pixels)
Specimen background
laser power (%) mean STDEV mean STDEV
0.1 9.36 7.62 0.67 2.13
0.2 11.3 8.42 0.65 2
0.3 13.26 8.89 0.65 2
0.4 15.21 9.69 0.67 2.1
0.5 16.85 10.22 0.68 2.09
1 45.54 16.63 0.68 2.13
2 82.51 22.64 0.67 2.15
4 155.69 31.58 0.66 2.09
8 297.19 43.26 0.73 2.19
16 567.71 60.79 0.79 2.32
32 1049.43 82.74 0.86 2.36
So it seems that I can count about 100 photons per microsecond without
having to worry too much about the pile-up. Does anybody know how how the
Olympus's "Hybrid photon counting" works?
Spreadsheed file with more details, graphs are here:
http://microscopy.tamu.edu/instruments/light-microscopy/fv1000-tests
This folder also contains some of the image files.
Sincerely,
Stan Vitha
Microscopy and Imaging Center
Texas A&M University
|
|
|