Section 1 Problem Countermeasures
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1.
No fluorescent light
image.
2.
No transmitted light
image.
3. Images are disrupted.
4.
Visibility is
poor.
5. Bluning and uneven
clarity.
6. Flare is visible.
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The photomultiplier of the
channel set with the
detection mode setting knob
is not set.
The transmitted light
detector is not correctiy set.
The
U-ansmitted
light
filter
at
ttie microscope base is in
the light
patti.
The absorption filter is in the
light
path.
Too much vibration at the
setting location.
Fluorescent or other extemal
light is being detected.
The analyzer is in the light
path.
Scanning speed is fast
The fluorescent light dye
color and absorption filter
are not matched.
The excitation light is too
weak.
Too much vibration at Uie
setting location.
The specimen is mounted
inclined.
Non-fluorescent glass is not
being used.
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Check the [Chi] and [Ch2]
check boxes of the [Acquire]
panel.
Con-ectly set ttie transmitted
light path selector knob of
Uie transmitted light
detection unit.
Correctly set the detection
mode setting slider of the
scan unit
Remove the fllter from the
light
patti.
Remove the absorption filter
in the ti-ansmitted light
detection channel of the
scan unit from the light
path.
Consult your Olympus
dealer.
Darken the room and read
the image again.
Remove ttie analyzer from
the light
path.
Lower the scanning speed to
an appropriate speed or
integrate the images.
Select an absorption filter
that matches the fluorescent
light dye
color.
Refer to Operation, 4-1-2
Scan Unit Setting. Follow the
instmctions in the
[Microscope Configuration]
window.
Change to a high
transmission ratio ND
filter.
Consult your Olympus
dealer.
Set the specimen con-ectty.
Use non-fluorescent glass.
?Manual!Reference^
Hardware, 2-1.
Operation,
4-1-3-3.
Hardware, 3-2-3.
Hardware, 2-1,
3-2-4
Hardware, 2-2,
3-2-3.
Hardware, 3-2-5.
—
•
—
Hardware, 3-1-2,
3-2-3.
Operation,
4-1-3-11,
4-1-5.
Operation,
4-1-2.
Hardware, 3-1-5
and 4.
Hardware, 2-1,
3-1-6.
—
Refer to the
microscope
instmction manual.
1-2
