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Nikon Optiphot Quick Reference Manual
Nikon Optiphot Quick Reference Manual

Nikon Optiphot Quick Reference Manual

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Quick Reference Guide to Using the Nikon Optiphot
1. Epi-fluorescence.
1.1. Turn on the xenon lamp before anything else
1.1.1. Power supply on shelf above microscope
1.1.2. Press black rocker switch
1.1.3. Press the orange button momentarily, and release
1.2. Turn on the microscope lamp
1.2.1. Green push button at left, front base of microscope
1.3. Select your objective lens;
1.4. Select desired epi-fluorescent filter with slider over objective turret
1.5. Open fluorescent shutter
1.6. Set the trinocular beamsplitter to direct the image to the eyepieces;
2. Brightfield.
2.1. Turn on the microscope lamp
2.1.1. black push button at left, front base of microscope
2.2. Select your objective lens;
2.3. Set the trinocular beamsplitter to direct the image to the eyepieces;
2.4. Select "DIA" on filter slider;
2.5. Adjust lamp intensity with slider across base of microscope
2.6. Focus on the specimen
2.7. Set Koehler illumination
2.8. See following pages for use of condenser for darkfield and phase contrast.
3. Turn off the equipment.
3.1. Switch off the xenon lamp
3.1.1. Lamp must be on for at least 30 minutes
3.2. Turn off the transmitted lamp
3.3. Remove slide
3.4. Clean any immersion oil or mounting medium from lens and stage
Did you record your usage on the Nikon reservation calendar?
July 29, 2016
Digital Microscopy Center, University of Washington
(Details begin on following page)
Start-up
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1

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Summary of Contents for Nikon Optiphot

  • Page 1 3.1.1. Lamp must be on for at least 30 minutes 3.2. Turn off the transmitted lamp 3.3. Remove slide 3.4. Clean any immersion oil or mounting medium from lens and stage Did you record your usage on the Nikon reservation calendar? July 29, 2016...
  • Page 2 Digital Microsopy Center, University of Washington Details on Getting Started With The Microscope See the Nikon Optiphot manual for additional information about the microscope. Start-up 1. Epi-fluorescence. 1.1. When using fluorescence, turn on the mercury lamp before anything else; 1.2. The xenon arc lamp power supply sits on the shelf over the microscope;...
  • Page 3 Digital Microscopy Center, University of Washington Condenser focus Substage field diaphragm Fine Focus Coarse Focus Transmitted Light ND Filters “Photo” switch Brightfield lamp power Brightfield lamp voltage Figure 1. Sub-stage Controls Filter Light Reduction % Transmission ND2 1/2 50% ND4 1/4 25% ND16...
  • Page 4 Digital Microsopy Center, University of Washington 4. Select your objective lens 4.1. Choose the objective lens compatible to your specimen and needs 4.1.1. low NA will provide low resolution and weak fluorescence, but large working distance 4.1.2. low magnification providse large field of view but may not magnify sufficiently for full resolution at the camera Locking screw for stage rotation.
  • Page 5 Digital Microscopy Center, University of Washington A. Performing Brightfield transmitted light microscopy 1. Focus on specimen 1.1. Place slide on the stage and hold in place with the stage clip 1.1.1. Begin with low magnification for greater ease in surveying your specimen to identify regions of interest 2.
  • Page 6 Digital Microsopy Center, University of Washington 6. Controlling epi-fluorescence 6.1. Select filters for specific wavelength bands (“colors”) by the black slider located on the front of the microscope betwee the eyepieces and objective lens turret; 6.2. There is only room for 3 filters cubes 6.2.1.
  • Page 7 Digital Microscopy Center, University of Washington Filter Label Cube Label “Color” Part Nikon FITC HQ:FITC green 96170 C01174 TxR HQ:TXRD red 96172 C00178 UV-2E/C blue blue Cy5 Cy5 far red 31023 C81736 Table 3. Epi-fluorescence filter choices Lens µm/pixel pixel/µ 1 mm reticle field 1/.04 Plan 160/-...