21
II. Microscopy Method
4
Return to the bright-field microscopy under the
episcopic illumination.
1
Pull out the analyzer slider to remove the analyzer
from the optical path. (See Page 60.)
2
Pull out the polarizer slider to remove the polarizer
from the optical path. (See Page 57.)
3
Pull out the DIC slider to remove the DIC prism
from the optical path. (See Page 64.)
4
Pull out the lambda plate slider to remove the
lambda plate from the optical path.
(See Page 62.)
5
Operate the EPI brightness switch on the
operation panel to adjust the brightness of the
episcopic illumination. (See Page 42.)
6
Adjust the brightness with ND filters.
(See Page 44.)
5
Rotate the rotation ring of the polarizer slider to adjust the contrast. (See Page 57.)
The polarizer slider is equipped with the 1/4 lambda plate so that the contrast can be adjusted by
adjusting the orientation of the polarizer.
6
To perform the sensitive color microscopy, push in the lambda plate slider to place the lambda
plate into the optical path. (See Page 62.)
7
Adjust the EPI brightness switch on the operation panel to adjust the brightness of the episcopic
illumination. (See Page 42.)
8
Adjust the brightness with ND filters. (See Page 44.)
UEPI2
A
USB
RS23
2C
LCNT
ND8
NCB
F.S.
Achr N.A = 0.9
JAPAN
0.8
0.7 0.6
0.5 0.4 0.3 0.2 0.1
3 x 2 ST
AGE
JAPAN
F
.
STOP
JAPAN
BF
DF FL1 FL2
FL1
FL2
100
20
0
100
IN
OUT
LV-TT
2
OBJ.
CUBE
A.S.
EPI
DIA
EPI
DIA
3
Operation
panel
6
EPI brightness switch
5
1
2
6
5
4
Содержание Eclipse LV100DA-U
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