Zeiss Axiovert 135M Manuel utilisateur
Directions for Zeiss Axiovert 200M
START UP
1. Turn on mercury lamp controller (#1). Wait a few seconds to make certain lamp is
on.
2. Turn on the x-y stage controller (#2)
3. Turn on the camera controller (#3)
4. Turn on the microscope (#4) (green button on the right side of the microscope.
5. Login to the computer with your CNET ID and password. Double click on the
Openlab program on the computer.
IMAGING
1. Choose the correct stage for slide or dish. Make sure the stage is properly inserted
(there is a spring in the corner). The stage should be laying level: Don’t have one
side higher than the other- it should not wobble. If your sample is on a slide, make
sure the coverslip is facing down. Choose the objective you want by moving it in
to place or choose the objective on the Microscope palette. The dry objectives are
10x, 20x, and the first 40x. If you are using an oil objective (the second 40x, 63x
or 100x) put 1 drop of oil directly onto the objective. When focusing with the oil
objective you should have a space of oil between the objective and the cover slip.
The objective and cover slip should NOT be touching.
slide
Coverslip
2. Check the fluorescent palette in the program: if the filter you need is not in place,
use the red- handled Zeiss tool and unscrew the screw that holds the reflector
turret in place with 2 turns. (DON’T unscrew until the screw falls out). Gently
push the reflector turret out and exchange filter cubes. (Do not touch the actual
filters with your fingers). The cubes should all be level to each other if properly
inserted in the turret. Carefully replace the reflector turret (it should be smooth
and easy to insert- do not force it! If you are forcing it, then you are inserting it
incorrectly, and it will get jammed!) Use the Zeiss tool to lock in the reflector
turret after changing your filter. Then change the label for the filter in the reflector
pallet in the program.
3. If possible start by imaging your sample using transmitted light to prevent
bleaching. Click on Transmitted Light or the dic (#5 position) in the Zeiss
reflector palette and focus using the focusing dial on the right side of the
microscope. (Do not open the fluorescent shutter at any time while on
transmitted light!) Use Koehler illumination to focus the condenser for
transmitted light every time you switch to a new objective. For transmitted light,
choose the camera shutter that sends 50% of the light to the camera and 50% of
the light to the ocular.
a. Koehler Illumination: After focusing on your sample with transmitted
light, close the diaphragm, and use the condenser-focusing knob on the
right side of the transmitted lamp to focus the condenser unit so that the
diaphragm is sharply focused. You should now see your sample and the
Oil objective
oil
Directions for Zeiss Axiovert 200M
diaphragm – both in focus. Now center the diaphragm using the centering
screws. Choose your image and place it in the center of the field. Then
reopen the diaphragm just until the camera no longer sees it. Look at the
computer screen and click V on the keyboard for viewing the live image.
b. Exposure: click on AE on the Video controls palette to get an automatic
exposure. You can adjust it manually as well by double clicking on the
time and entering it from the keyboard or clicking on the up or down
button. Make sure that the image on the screen is focused and tap the
Space Bar on the keyboard to take a picture. You will see the picture you
just took on the layers palette. To label your picture, double click on the
word “captured layer” and type in your label.
4. Set up your State Saver for transmitted light using brightfield, phase, or DIC and
matching the lens to the objective that you are using (i.e. phase2 for 40x dry).
Save your settings with the edit pencil on the State Saver palette by deselecting
previous settings and selecting your new settings. Thereafter, just hit RESTORE
when you want to bring the particular filter settings up again.
5. Set up your State Savers for fluorescence as well. To colorize your fluorescent
image using the State Saver, highlight the camera layer and choose a color from
the color table on the left of your image. Send 100% of the image to the camera
and set the exposure. Increase the gain if the exposure is too long (i.e. 5 seconds)
to shorten the exposure. Make sure your images are focused on the computer
screen and take the picture using the space bar. Initially save your working file as
a LIFF file. As you take pictures, update your working LIFF file with APPLE-S.
When you are finished select all of your images and save as MULTIPLE TIFF
FOR PUBLICATION (For Photoshop- millions of colors) or MULTIPLE TIFF
(For ImageJ- 12 bit grey scale). Save onto a CD or your memory stick or onto
your server folder. If you save onto the server, be aware that the files get
automatically deleted every Sunday after 1 month. If you have old files (older
than 1 month), they will get deleted on the first Sunday!*@!>!
If someone that needs to use the microscope after you, log off of your account, and
leave the microscope on for them. BUT if they are not physically there and if the
technical director is not in the facility, then TURN OFF the microscope.
SHUT DOWN
1. When you are finished, quit the Openlab program (Apple-Q)
2. Turn off the microscope (#4)
3. Turn off #3
4. Turn off #2
5. And lastly, turn off the mercury lamp (#4)
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