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In this technique, the shape change of the cartilage disk was visualized while the cartilage was immersed in physiological solution and compressed in unconfined geometry.
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Coverslips were immediately mounted onto slides with 4′, 6′-diamidino-2-phenylindole (DAPI; Vector Laboratories, Inc .. Nuclear morphology was visualized using spinning disk confocal microscopy.
The microcirculation of the cremaster muscle was prepared for microscopy as described above and was visualized using a spinning disk confocal microscope.
β-catenin expression was visualized by immunofluorescence using a Quorum Spinning Disk Confocal Microscope.
EGFP was visualized directly.
EGFP fluorescence was visualized directly.
Immunoreactivity was visualized by electrochemiluminescence.
Fluorescence was visualized with ApoTome.
The fluid flow through the double-disk pump is visualized using a red Rhodamine dye that is injected into the fluid passage upstream of the pumping volume.
Cells were visualized through a Spinning Disk Olympus DSU microscope, using a 60 × magnification, 1.42 NA immersion objective.
The spheres were visualized as cross-sectional disks overlaid on the particular slice from the data being displayed.
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