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In general spinning disc confocal systems perform optimally with adherent cells in culture and other relatively thin specimens. Thicker specimens with a large amount of out-of-focus fluorescence can be difficult to image because of a phenomenon called pinhole crosstalk.
- Start up and shut down procedure
- Specimen adapters available for the Vox and how to set up the CO2 supply
- Objective lenses
- Microscope filter sets
- Lasers
- Emission filters
Using the Vox
- Start up and shut down procedure
- Using the Nikon TiE microscope
- Coming Soon - Familiarising yourself with the Vox user interface
- Further Information
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