• Avoid touching lens surfaces with the fingers or with any rough material. For dusting, use a feather or a soft lens brush and then a washed-out soft cotton cloth only to wipe off finger marks or grease, wet the cloth with xylor, but never with alcohol or ether. The microscope body surfaces should be dusted in the same way and may slightly be oiled,
• Tightness of the coarse focusing knobs should be adjusted, in this type
ring,
(L-Ke) of microscope, by means of the adjustingknobs.
• Dismantling of the internal optical parts and the microscope body should not be attempted, because it may interfere with the performance of the instrument. It can be accomplished only by an expert or the original manufacturer.
• Do not apply any grease of not specified type to the sliding surfaces of the coarse focusing adjustment and of the floating stage. If necessary, ask for your dealer or the manufacturer.
• The microscope is to be used at a dust-free place. Avoid any forcible manipulation of the moving parts. At all times the instrument is to be handled carefully e.g. for carrying the microscope, hold its base with one hand and its arm with the other.
• When not in use, it should be covered with the vinyl cover or kept in the wooden cabinet which is available on order. Store it at a dry place. It is recommended to keep the objectives and eyepieces in a desiccator.
Number 50mm 21.0 With adjustable eyepiece collar 25mm
25 mm
50mm 25mm ^17nim
25mm 18.0
18.0 With adjustable eyepiece collar
18.0
8.0 General purpose
21.0
12.0
8.0
7
-
Working Distance
9.50lim
7.10mm
5.70mm
0.54mm
0.54mm
Spring-loaded
0.52mm
No cover glass type
0.16mm
0.16mm
Spring-loaded
0.16mm
With iris diaphragm
29.7mm
35.6mm
28.6 mm
18.2mm
7.0mm
0.24mm
Spring-loaded
0.32mm
Spring-loaded,
0.12mm
Spring-loaded
0.12mm
Spring-loaded
0.19
mm'
Spring-loaded
0.10mm
Spring-loaded
2.0 mm
For tissue culture observation
6.4mm
Dark Contrast
6.4mm
Bright Contrast
4.5mm
Dark Contrast
4.5mm
Bright Contrast
0.54mm
Dark Contrast, Spring-loaded
0.54mm
Dark Contrast
0.54mm
Bright Contrast
0.16mm
Dark Contrast
0.16mm
Dark Contrast
0.16mm
Bright ContrastDark Contrast
2.0mm
(For tissue culture work)
15mm
7.1 mm
5.7mm
0.52mm
0.16mm
7.0mm
0.32mm
Spring-loaded
0.12mm
Spring-loaded
Remarks
High-power purpose
General purpose General purpose General purpose
Supplied together withWith
5X, lOX, 15X
lines
for
picture frames plus cross-
framing
and
Remarks
for
no
cover glass type
//
//
n
if
"U"
eyepiece tube
focusinsf
dark-field
3.
Combinations of Objectives and
Eyepieces
Total magnifying power obtained by the combination is the product of
individual objective power multiplied by individual eyepiece power. A selection
of the combination
will
be decided so as to get the highest resolution of the image (resolving power), the largest extent of object area
(real field) which can be observed without moving the stage or
slide,
or the greatest thickness of object (depth of focus) which can
be
distinctly
depending
are
the results compiled
and
eyepieces:
Objective
Objective
4X
lOX
20X
40X
lOOX
•
The working distance is the
cover
glass
seen
without raising or lowering the microscope stage,
upon the purpose of using the microscope. Shown below
from
the different combinations of objectives
Resolution
Eyepiece
Eyepiece
5X lOX 15X
5X lOX 15X
5X lOX 15X
5X lOX 15X
5X lOX 15X
Total
Total
Magnifying
Magnifying
Power
Power
20X 40X 60X
50X lOOX 150X
lOOX 200X 300X
200X 400X 600X
500X
lOOOX 1500X
Working Distance
(mm)
9.5
7.1
5.7
0.54
0.16
clearance
Minimum Resolved
in object
(^)
2.7-5.5
1.1-2.2
0.69-1.38
0.42-0.84
0.22-0.44
Distance
or
in image
(mm)
0.05-0.11
0.11-0.22
0.16-0.32
0.05-0.11
0.11-0.22
0.17-0.33
0.07-0.14
0.14-0.28
0.21-0.42
0.08-0.17
0.17-0.34
0.25-0.50
0.11-0.22
0.22-0.44
0.33-0.66
Real Field
of View
(mm)
5.25
4.5
3.5
2.1
1.8
1.4
1.05
0.9
0.7
0.52
0.45
0.35
0.21
0.18
0.14
Depth
Focus
(^)
100
1.8
1.2
1.0
0.6
0.44
0.38
between the upper surface of the
and the lowest edge of the objective critically focused. Note
of
64 52
16 10
8 6
4 3
that, as shown in the above table, the working distance becomes very small
for
high
power objectives.
•
The resolution of minimum resolved distance (the limit of resolving power)
is
the minimum distance between object points discernible as separate
under
the microscope illuminated by the
The shorter the
is,
the small resolving distance results. In the table, the smaller values
indicate
central
#The
the resolution obtained by oblique and the larger values by
illumination, (see "Illumination" on page 11)
minimum resolved distance in the image is the value in the object
light
wave length, the higher the resolving power, that
light
of wave length
550myu.
multiplied by the total magnification of the microscope. If the resolving power of the microscope is important, choose the eyepiece by the use
of which the image resolution comes—0.3mmaccepted
(when the object is
seen
criterion on the upper limit of the total magnification of a
within
from
the distance
that of the naked eye
25mm);
generally
0.15
-8-
Page 6
microscope set up is about
500—lOOOX
of the numerical aperture of the objective to be used. Note that in photomicrography it is useless to raise the magnification beyond the resolving power of the emulsion (usually aboutis
higher than that of the naked eye, photographs are usually taken at
0.05mm).
However,
since the resolution of the emulsion
a lower magnification and thereafter they are enlarged.
•
Real field of view (in mm) represents the extent of the object that comes
under observation. In higher magnification it becomes extremely
small. Consequently, it is advisable to take aim at the object point to be exa-mined
first under lower magnification and then revolve the nosepiece to
higher magnification.
•
When focus is on the center of the
blurred,
because a curvature of the image plane is unavoidable in the
field,
its circumference will usually be
microscope, except when using a plan type objectives. In order to get sharp corner image, it is necessary to adjust the fine focusing knob and switch the focus from the center onto the corners.
•
Depth of focus represents the thickness or height of the object in fi sharply
seen when observation is made through the microscope. In photomicrogra-phy the depth of focus becomes smaller than the figure shown in the previous table. Therefore, careful attention must be made in focusing
when
taking
microscope pictures. By closing the condenser diaphragm, the depth of field can be made greater than the value shown in the table.
4.
Condensers
Type Abbe Abbe Aplanatic
Achromatic
Achromatic (long focal-length type)
Universal Dark-Field
Low-Power
These
condensers are not only capable of concentrating light-beam for better illuminationtion
of microscope image, image contrast and depth of focus. In precise
Condenser
Condenser
of the image
Numerical Aperture
1.30
Two lenses
1.30
Two lenses
1.40
Three
lenses
1.25
Five
lenses
0.7
Four
lenses
1.20-1.40
for
dark-field
Single lens
field,
but also gives a great influence on the resolu-
For central illumination (without oblique illumination slider) For central and oblique illumination (with oblique
nation
slider) For high-class microscopy For high-class microscopy
Long focal-length type. Working distance 12mm. With turret-mountedphase-interference microscopy. Supplied in centerable mount. With outer diameter 36.8
mm.
Objectives to be used lOX up to
for
fluorescence work.
built-in
adjustable iris diaphragm. Thickness of slide glass
to
be used, must be less than
For low-power macro-objectives, e.g., 1.2X, 2X, & 3X Plan Achromatic
Remarks
illumi-
annular diaphragms for phase-contrast and
lOOX.
lOOX
objective used should have
1.2mm.
Ideally suited
observation and photomicrography, the use of an achromatic or aplanatic condenser with the maximum numerical aperture 1.25 provided with an oblique illumination device and a filter case is specially recommended.
—
9 —
ATTACHING
THE LENSES
Before attaching the objective and the eyepiece to the microscope, first clean their outer lens surfaces.
often
interfere with the image contrast.
1.
Mounting
Take
special care in handling the objectives.
the
Objectives
Even
a slightly stained finger mark may
Before attaching the objectives on the nosepiece revolver, lower the microscope stage sufficiently. Securing each objective with the fingers
of one hand, screw it into
each nosepiece hole with those of the other hand (Fig. 4).
It
is recommended to
mount
the objectives on the nosepiece or-derly from low to high
powers so that the
magnification
of each objective augments as the
revolver is rotated clockwise or counter-clockwise.
Microscope Model L-Ke has on its upper surface of the nosepiece revolver
five
blank spots (Fig. 5) on each of which the objective magnification can
be Inked solookingtions
from above, the
that,
by
these Indica-
objective located below can be identifiedout
having to turn away
your
the
eyepiece.
eyes
with-
from
When rotating the re-volver, hold its outer milled
rim with
thumb
and first finger,
but
do not push the
your
objective barrels, other-wise alignment of the objectives may be
trou-
bled.
-10-
Page 7
2.
Mounting the
Eyepieces
For mounting, simply droprecommended
to
leave
an
the
eyepiece
eyepiece into
in
place even when
the
eyepiece tube.
it is not in use, in
order
to
prevententrancetheputcap
of
dust into eyepiece tube. on the
in
eyepiece
placeeyepiece removed.The inclined eyepiece body
tube,
trinocular, bino-
cular
or
monocular,can
be rotated after loosen-
ing
the
clamp screw
(Fig.
6) for
ence
in
viewing from any desired direction without
moving
It is
the
Or
of the
conveni-
the
Resolution
and
illumination.
1.
Condenser
Stop downtion
the
from center
higher becomes
object
by
increased
(Fig.
8, a, b).
ILLUMINATION
contrast
Iris Diaphragm and
condenser iris diaphragm
to
the
of
image
are
edge.
The
farther
contrast
and
and
resolution, which distinguish details
unsymmetrical shadow
Images
the
greatly affected
and
slide
it in the
iris diaphragm
at the
by the
radial direc-
is
off-centered,
boundary
method
of
object
of
the
of
microscope stand.
can
be
removed
3.
IVIounting the
To
mount
the
By
further releasing
and
replaced with another type eyepiece body tube.
Condenser
condenser, unlockbeneath the condenser holder
as far as itgo. Then, tightenlock screw.case locate
In
the
will
the this dia-
phragm eccentering lever
and itsa proper placeto
facilitate their manipulationhand
(Fig. 7). The correct distancetain
immersiontweenface
of the
the
top of
is secured when
condenser
the
lower sur-
condenser
is
screw
so as
with
oil be-
slide
raised
at
one
to re-
and
the
to the
knob.
upper
the
lock screw,
limit
the
by
turning
clamp screw
and
insert
the
condenser focusing
the
the
body tube
condenser
(a)
Central illumination (b) Oblique illumination (c) Dark field illumination
When
the
iris diaphragm
the
object
at anobjectiveresolutionIfintroducenation will
the
the
resolution reaches maximum
by
central illumination.
diaphragm
the
light bundle directly into
be
obtained.by various angle illuminationsfavorableInopening
thefieldsmaller,ifaperture,If
for the
the
central illumination
of the
objective.
In
illumination
the
contrast
the
iris diaphragm
the
decrease
the
diaphragm
iris diaphragm just corresponds
is
positioned
angle
o'f
incidence
is
further eccentered
If the
object
may be
the
this case
excessive
are cut off and
is
enhanced, though
is
large enough
of
resolution will
is
stopped down
so as to let the
the
same
as the
and
to
such
the
objective, dark field
iris diaphragm
are
integrated.
is
An
included.
maximum resolution
to the
outer
rays
flare
is
minimized.
the
resolution
to
cover
60-70%
not be
to
minimum
remarkable.
for
light bundle enter into
aperture angle
twice
as
much
an
extent
as not to
widely opened, images
illumination angle
is
obtained when
aperture angle
to be
If the
used opening is
lowered.
of the
admitting only
of the
as the
illumi-
not
the
of
as
dark
is
made
But
objective
very
-11—
—12—
Page 8
small
light bundles, the effects by diffraction, reflection, refraction, etc., may be exaggerated so that fringes may be seen at the image edges which may likely induce misinterpretation of the image, but it may be effective for special occassions (e.g. definition of general structure of non stained
specimens). (Fig. 8, c).
2.
Light
As already cited, the iris diaphragm plays an important role In thenationthatobjective being used, in order to obtain the maximum resolution. In
user, however, may dispense with such a procedure, and will obtain the same result by adjusting the diaphragm opening until satisfactory distinct-ness of the image is obtained.
If a high resolution and, at the sameoblique illumination will be effective.specimens, transparent phase-contrast specimens, etc.
illumination,
it
is necessary for observation to change the direction of illumination, by turningThe condenser aperture is off-centered in any direction by rotating and at the
done only by using one hand, the thumb and the first finger for off-centering
and the middle finger for opening or closing the diaphragm. (See Fig. 9).
3.
Condenser
The condenser focusing is made by turning the condenser focusing knob. This
Source
illumi-
on microscopy. As a principle the diaphragm should be so adjusted
the numerical aperture of the condenser is equal to that of the
practice, however, to keep out stray light which would reduce image contrast, closing the aperture of the condenser down to 60-70%
of that of the objec-tive lens will bring about a good result in most cases. The coincidence of condenser diaphragm aperture with the opening (exit pupil) of the objec-
tive can be ascertained
by looking through the microscope tube after re-moving
the eyepiece and
closing the diaphragm
slowly. An experienced
time,
a high contrast are desirable,
This
is suited especially for lowdyed
However,
a remarkable polarity in contrast and resolution may appear;
the iris diaphragm.
same time by radially sliding the diaphragm.
Focusing
manipulation is necessary only in case of Koehler illumination or dark
Knob
-13-
This
manipulation can be
in this
field
observation. The condenser is usually to stay at the upperneed not to be lowered, except when a stray image of an outside object superimposes the specimen image too sharply in such a case as in direct sun light illumination or as some uneven brightness interferes with the observation.
4.
Brightness
For this purpose adjust the voltage of current supply by regulating the
transformer of the illuminator or by using a proper neutral density filter. Adjustment by means of the condenser diaphragm is not at all possible.
5.
Preparation
(1) Lamp and Socket
As shown in Fig. 10, lining
up the red dot on the socket
retaining
the
lamp housing, fit the
socket to the housing by
bayonet fashion.
(2) Centering and Focusing of
the
Lamp Bring the illumination change-over lever in the position "M". Stop down
the
condenser diaphragm beneath the microscope
stage. Move the lamp back and forth to bring the image of the filament into sharp focus on the bottom sur-face of the diaphragm. For this
purpose, it is conve-nient to utilize the reflection on themirror,ring
to fasten the lamp socket in position. Bring the illumination change-over lever to the position "H". Manipu-lating
condenser diaphragm.
(3) Centering of the Illumination Field Diaphragm
Stop down the opening of the illumination field diaphragm to about 2mmViewing through the microscope, focus the objective 40X to the image of specimen.
Moving up and down the condenser, make a sharp focused image of
the
illumination field diaphragm on the specimen.
Adjustment
and
Adjustment
ring to that on
accessory as shown in Fig. 11. Then, turn right or left only the socket
the lamp centering screws, make centering of the image on the
in diameter.
reflecting
—
14—
limit
and
Page 9
Manipulate two centering screws until the image of the illumination
field
diaphragm comes to the center.
You need not mind about a slight deviation from this centering caused
by switchingany objectionable result.
6.
Observation
For usual case of observation with objectives from 4X tosion), it suffices to leave the change-over lever at the position L. When an exact illumination or extreme brightness is required, as is the case with photomicrography, it is necessary to make adjustment for each magnifi-cation by switching
7.
Photomicrography
Make exact adjustment, depending upon the magnification of the objec-
tive being used, by switching the change-over lever as below:
over
to other objectives because this will not produce
lOOX
(oil-immer-
over
the lever.
lens. A filter of the diameterin
the filter case of the microscope.
the
microscope base is available on order.
33mm
can be placed in the condenser or
This
filter case to be attached onto
FOCUSING
1.
Focusing
The microscope model L-Ke is provided with coaxial, coarse and fine focusing knobs, both of which are located near the microscope base (Fig.
13).
Forward rotation of either of the focusing knobs by the operator raises
the
microscope stage and vice
Adjustment
versa
(Fig. 13, 14).
Objective magnification 4X Position of the change-over lever L
10-20X
M i H
40-lOOX
i
When using an objective 3X or lower, set the change-over lever to H and replace the condenser with the one specifically designed for lower magnification.
The illumination for the Model L-Ke will not change its color temper-
ature by the change-over above mentioned.
8.
Other
When using any other
lightthethe
lens with thereflectingshown in Fig. 12.
9.
Filter
A filter of the diameter
Light
Sources
source outside of microscope, replace illumination field
accessory
mirror, as
Case
45mm
can be mounted on the illumination field
—15—
2.
Eyepiece
When using a binocular or trinocular eyepiece tube for observation the adjustmentright
and left
ring
on the lefthand eyepiece. After focusing withstage, turn the adjusting ring left or right to obtain the sharp image with your
left eye, too. Then, regulate the interpupillary distance of the bino-cular or trinocular tube by sliding the eyepieces left or right by means of the
knob (Fig. 15), until the viewfields of both eyepieces merge together.
It
will be advantageous to memorize the attained diopter and inter-pupillary distance readings for future use. The red dot engraved on the interpupillary distance scale indicates the position where the mechanical tube length becomes exactlyHK (high eyepoint type) eyepieces have an eyecup on top, the rotation of
Adjustment
of the user's eye-sight (diopter) discrepancy between the
eyes
is necessary which is made by rotating the adjusting
your
right eye by raising or lowering the microscope
—
16—
160mm.
The
Page 10
which will give proper eye-to-lens distance.eyecup should
3.
Coarse
The coarse adjustmentadjusting
If
the
revolution
justing
ring counterclockwise.
clockwise turning.
Never
twist
microscope whose focusing knobs, coarse
(not coaxial). Focusing
microscope stage untilobjective becomes less longer thanto
be
used
the
stage until
4X,
lOX, 20X, 40X and lOOX
mately
in
of
the
fine focusing knob only being required
4.
Preset
The right-hand focusing knobWhen
theengraved besides) untilin
the
direction
be
screwed
Focusing
ring:
of the
the
focusing knobs
(see
table
the
focus when revolved into position
Device
lever
is
fastened
to
drive
in.
may be
coarse focusing knob
may be
the
on p. 8),
specimen
it
stops,
the
eased
Too
much tightness
for
this adjustment
performed
distance between
the
then looking through
to be
objectives
has a
by
turning clockwise
the
coarse focusing knobs cannot
stage closer
—
17--
or
working distance
examined
are
preset lever
to the
For
those wear eyeglasses,
tightened
is too
and
as
is parfocal
one
for
objective.
by
means
loose, turn
may be
fine,
follows: First, raise
the
plainly visible.
critical focusing.
on its
(as
adjusted
as in the are
located separate
specimen
of the
the
eyepiece, lower
, and are
after another,
drum
indicated
This
of the
the ad-
by the
traditional
and the
objective
approxi-
the use
(Fig. 16).
by the
arrow
be
turned
presetting
the
is
utilized
for
quick refocusing
after
the stageand outfocusedthe
specimen
mersion oil.when fastened, preventssame
timeingtheglass.
5.
Fine
Manipulationing
knob
a.
To
obtain the sharpest image.
b.
To
transfer
centerviewfield.
c.
To
focus upond.
To
correct a slight blurring which
slide.
e. Tomeasure
The microscope
knob
raises
reading
range
of
6.
Oil
When usingminutenecessaryimmersion
the
slide
mersion observation
jective
(dryviewfield.scope stageapplying a dropto
the
preset
raising
carefully
oil
immersion
about
1/3
the
stage aboutAir bubblesmicroscope imagetube
without
of
the
nosepiece revolver,
or
by
means
Remaining
has
been lowered
for
changing
or
applying
The
preset device,
the danger
objective front
Focusing
of the
is
necessary:
to a
or
on the
fine movement
Immersion
lOOX
space (0.1mm) between
to
attain
oil is to be
as
well
system), bring
Set the
and
limit.
forward rotation
in the
the
of a
stiffened
of
and
fine focus-
the
focus from
corner
of the
the
different layers
the
thickness
is so
designed that
lowers
the
right-hand knob scale
objective,
the
filled between
as
between is
performed
preset lever
revolve
of
immersion Then, focus
the
stage
lOOX
objective
0.08mm immersion
and are
eyepiece,
needle.
oil may
im-
at the
damag-
slide
of a
thick specimen.
may
take place when shifting
of
object under examination.
one
revolution
microscope stage
is
38mm;
the
the
application
the
objective
specified numerical aperture.
the
objective
as
the
specimen
by
turning clockwise.
the
nosepiece revolver
oil
onto
up by
by
manipulating
is
designed
of the
closer
can be
by
fine focusing knob, that
to the
oil,
visible when looking into
removed
adding a certain quantity
often impair
18
0.2mm.
up to
0.002mm
same
as of
coarse focusing.
of
immersion
top and the
the top
follows: First, using
objective from
which
lens
of the
and the
in
focus
and in the
to lOOX
the
cover
glass, raise
looking through
the
fine focusing knob.
to
attain
its
may
sometimes intervene
by
repeating slight movement
the
image. Therefore,
of the
This
For
cover
the
fine focusing
permits direct
(2«). The
oil in the
cover
critical work
condenser
glass.
lOX or 40X ob-
center
Lower
critical focusing
the
objective. After
the
the
eyepiece
is,
parfocal position.
the
microscope
of
immersion
the
whole
glass
is
the
and
Oil im-
of the
micro-
stage
up
and
The
by
bringing
the
oil
im-
Page 11
mediately after finishing the work, clean off the remaining oil from the lens using a soft cotton cloth wetted with xylor. Never use alcohol or immerse the top of the objective in xylor. Be careful not to use immersion oil that has been thickened by age. The refractive index of the immersion oil should be
7. Long Working Range of the Stage
The microscope L-Ke is designed to permit large-range lowering of its stage
(71mm) for convenience
in observing a thick speci-men such as for metallurgy or culture. Unlock the lock screw beneath the stage
(Fig.
17), and the stage
can be lowered 33mm ^^^^^^^ and by manipulation of
the coarse focusing knob farther 38mm. The stage lowered to such a great extent may be useful in macrophoto-graphy or when a special stage is used.
8. Exchanging the Stage
Lower the stage by means of the coarse focusing knob and then unlock
the stage lock screw. The stage, then, can be removed.
^^W^^^^^gnm^^j^^^^
1.515.
'[J
MOVING THE SPECIMEN ON THE STAGE
1.
Rectangular Mechanical Stage '*R"
This stage enables fine crosswise travelling of the slide in the range
of 50 X 75mm, allowing reading of the movement down to 0.1 mm by the use of the vernier provided. For securing the slide on the stage in position, open the clip. Each travelling is performed by rotation of two coaxial knobs iDcated
one above the other on
the vertical rod protruded
below on the left side from
the front, the upper knob being
Clip
for longitudinal and the lower one for lateral travel of the slide on the stage. In fluorescence microscopy or in using oil immersion ob-jectives, where the clearance between the condenser and the slide also should be oil-immersed,
cause unsmooth travel of the
slide.
19 of the circular opening plate
at the center of the stage or fastening of the clamp screw will be helpful to a positive travel of the slide (Fig. 18).
By unlocking the lock knob on the edge of the stage the stage can be rotated horizontally for convenience in the observation from the opposite side of the microscope (Fig. 19), where the eyepiece tube is to be rotated
180°.
may often be of use in photo-
micrography, when the picture format is changed fromcal to horizontal or vice versa.
It is recommended to use the slide adapter on the stage
(Fig.
tudinal travel of the slide in such reversed position.
2.
Circular Floating Stage
The circular floating stage
(Fig.
smoothly and precisely in any desired direction simply by pushing the rim of the stage by the fingers, wichin a circle of 18mm in diameter. To fasten the floating stage in position, pressing the stage
stiffened oil may
In this case, removing
This rotation of the stage
verti-
20) for a sufficient longi-
21) glides and rotates
--19 —
Page 12
22
downward,stage counterclockwise.
Fasteningis necessary, when usingattachable mechanical stage
(Fig.
ableThe circular rotating stage type
permits measurementrotating angle
with
turn
the
of the
floating stage
22),
which will
on
order.
G is
also available, which
of
its
circular scale. (Fig.
rinn
of the
an
be
avail-
of the
specimen
23).
PHOTOMICROGRAPHY
The Microscope Modelwith light source builtperfect microphotograph only
the
microscope eyepiece with
toTherefore, when taking photographsfilm,
it is
recommendedexposure meter)exposure setting)
for
using with
Boxmethods, refer"AFM"
and any
L-Ke,
in the
to use the
or AFM
to the
general works
(with built-in exposure meter permitting automatic
and the
the
above attachments.
"Instructions
incorporating
microscope base, enables convenient
by additionally
any
Nikon Microflex Model
Nikon
F or
on
the
Koehler illumination device
mounting a camera connected
photomicrographic adapter.
of the
microscopic image
EFM
Nikkormat camera
For
details
of
Using Nikon Microflex
photomicrography.
or
of
photomicrographic
and
on
35mm
(with built-in
Nikon Dark
EFM" or
- 21 —
EXCHANGING
THE
OBJECTIVE NOSEPIECE
It
may
become necessary
the
to exchangenosepiecea seriesmetallurgical objectivesmountedobjective nosepiece. First, unlocklock screw,nosepiecearrowsertuntiling surfacesfit parallelFastenby means
(Fig.
in
of
phase-contrast
as a
and
in the
(Fig. 24). In
the
other nosepiece gently
it
stops, making
to
the
revolver
of the
25).
objective
such a case when
or
are
unit
on the
other
the
revolver
draw
out the
direction
of the
each other.
of the
place,
in-
the
guid-
dove-tail
in
position
lock screw
-22—
Page 13
7r
o
O
o
Q
Q
•D
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