beautypg.com

Troubleshooting guide – Olympus IX2 RFAEVA2 User Manual

Page 20

background image

17

TROUBLESHOOTING GUIDE

Problem

Cause

Remedy

Caution

L

aser beam

output

No laser beam is output

.

The laser oscillator is not ON.

Set the main switch and key of the laser oscillator to ON.

Never look into an objective

to check if the laser beam is

output

.

The illumination selector knob is set for the mer

-

cury burner illuminator

.

Push in the illumination selector knob to select the laser

illuminator light path.

The filter slider of the fiber light illuminator is pulled

out

.

Push in the filter slider to open the light path.

The manual shutter of the fluor

escence mirr

or unit

cassette is closed.

Release the manual shutter

.

Other fluor

escence mirr

or unit than a total internal

reflection fluor

escence mirr

or unit is engaged in

the light path.

Engage a total internal r

eflection fluor

escence mirr

or unit

in the light path.

The laser beam incidence angle adjustment knob

is turned too much counterclockwise.

Tu

rn the laser beam incidence angle adjustment knob all

the w

a

y clockwise.

The binocular tube shutter is pulled out

.

Push in the binocular tube shutter

.

Classification

It takes long time after the laser oscillator is

s

w

itched ON till the laser beam is output

.

The equipment is normal if the laser beam is out-

put within about 1 minute.

W

ait until the laser beam is output

.

The interlock k

e

y s

witch is set to OFF

.

Set the interlock key switch to ON.

The AC adapter connector is connected im-

pr

operly

.

L

aser beam

observation

Total internal r

eflection fluor

escence cannot

be obtained.

The laser incidence angle is not the critical angle.

Turn the laser incidence angle adjustment knob counter

clock

wise.

The laser beam incidence angle adjustment knob

is turned too much counterclockwise.

Turn the laser beam incidence angle adjustment knob

clockwise.

An objective other than the total internal r

eflection

fluorescence objectiv

e is engaged in the light path.

Engage a total internal r

eflection fluor

escence objective in

the light path.

Be sur

e to pulled out the shut

-

ter to block the laser beam be-

for

e pr

oceeding to tr

eatment

.

The specimen is tilted.

Place the co

ver glass so that it is par

allel with the stage

center plate.

The specimen being observ

ed has a r

e

fr

activ

e

inde

x of 1

.38 or mor

e (gly

cerin sealed specimen,

etc.)

Use the Apo1

00X

OHR objectiv

e (NA 1

.65) to observ

e a speci-

men with a r

efr

activ

e inde

x of 1

.38 (inde

x of c

ytoplasm) or

mor

e.

The immersion oil or cover glass is not suitable.

Special immersion oil and co

ver glass ar

e requir

ed when

using the Apo1

0

0

X

OHR (NA 1

.65).

Linear or elliptical interfer

ence stripes are

observed in the field.

The ND filter in the filter slider is tilted.

Stand the ND filter vertically using the ring spring provided

in the filter slider

.

If the interfer

ence stripe still does not disappear

, r

o

tate the

ND filter to minimize the interfer

ence stripe.

Be sur

e to pulled out the shut

-

ter to block the laser beam be-

for

e pr

oceeding to tr

eatment

.

If the interfer

ence stripe does

not disappear after tr

eatment

,

please consult Olympus.

A fluor

escence mirr

or unit incorpor

ating an e

xcita-

tion filter is engaged in the light path.

Engage a total r

eflection fluor

escence mirr

or unit without

excitation filter in the light path.

Random interfer

ence stripe is observed in the

field, and the stripe moves when the stage is

moved.

The specimen (cell) is not in close contact with

the co

ver glass but is separ

ated fr

om it at some

positions.

Put the specimen (cell) in close and perfect contact with

the cover glass.

The immersion oil contains bubbles.

Wipe off the immersion oil and attach new oil by avoiding

bubble penetr

ation.

Random interfer

ence stripe is observ

ed in

the field, and the stripe does not move even

when the stage is moved.

The

objectiv

e

is

dirt

y.

Clean the objectiv

e top lens with the cleaning mixtur

e fluid.

Connect it pr

operly

.

The specimen r

eplacement lid is r

e

m

o

ved.

Place the specimen replacement lid on the specimen

box

.

An interfer

ence stripe with a concentric pat

-

tern is observed.

Dust is attached to the dichr

oic mirr

or or barrier

filter

.

Blo

w dust a

w

ay using a blo

wer

, etc.