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Images of adult wings were photographed using a Zeiss Axiophot microscope mounted with a camera.
The sections were mounted and photographed using a Nikon Optiphot-2 microscope mounted with a Canon EOS 350D camera.
Montages of muscle sections were collected on a Zeiss Microscope mounted with a Leica DFC300 FX camera.
Slides were visualized at a magnification of ×1000 using a Olympus CX40 fluorescence microscope mounted with a DS-5Mc charge-coupled device camera (Nikon).
Light, DIC and fluorescence microscopy pictures were taken using a Zeiss Axioskop 2 Plus Fluorescence Microscope mounted with a AxioCam MRM digital camera, or alternatively with a Nikon Eclipse E400 microscope and a Nikon CoolPix 990 digital camera.
Immunofluorescent images were generated using a Leica DMI 6000B fluorescence microscope (Leica Microsystems, Bannockburn, IL) or an Olympus BX51 fluorescence microscope mounted with the Olympus DP71 camera (Olympus America Inc., Center Valley, PA).
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Ovules were dissected under a stereo dissecting microscope, mounted and sealed with coverslips.
With a fluorescence microscope mounted inside the cold box, they can search for the faint light emitted by fluorescing bacteria.
During flow cytometry experiments (see protocols below), small aliquots of cells were removed from the final preparations, air dried on a microscope slide, mounted with DAPI-containing mounting medium, and visualized in a fluorescence microscope to ascertain the quality of the staining.
A variety of means were employed for surface characterization, including a JEOL JSM-6400 scanning electron microscope (SEM) mounted with an EDAX Genesis 4000 energy dispersive X-ray (EDS) and A JEOL JEM-2010 scanning transmission electron microscope (TEM) adapted with a Gatan UltraScan camera using DigitalMicrograph was used to collect the desired images.
In the present work, an atomic force microscope (AFM) mounted with a diamond-coated tip was used to scratch through organic monolayer covered Si surfaces to create nanostructures by electrodeposition.
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