Titlebook: Confocal Microscopy; Methods and Protocol Stephen W. Paddock Book 19991st edition Humana Press 1999

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rvous system. A main theme in these examples is that the cell and tissue events are dynamic, on a time scale from minutes to days, covering spatial regions ranging in size from microns to millimeters.

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be either parameter insensitive, inversely sensitive, or exhibit a different sensitivity profile. Emission intensities for the two wavelengths are then divided by each other and thus the resulting ratio becomes normalized for inhomogeneities in probe distribution and concentration and in the system

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Imaging Sea Urchin Fertilization,, as the morphological features of most types of animal eggs are extremely well suited to the specific advantages this technology offers. Confocal microscopy is a powerful and flexible tool, and has been skillfully used and developed by a number of researchers not only to study the structural featur

厚臉皮

ostensible

Intracellular pH and pCa Measurement,be either parameter insensitive, inversely sensitive, or exhibit a different sensitivity profile. Emission intensities for the two wavelengths are then divided by each other and thus the resulting ratio becomes normalized for inhomogeneities in probe distribution and concentration and in the system

過(guò)度

Measuring Dynamic Cell Volume In Situ by Confocal Microscopy,ssues, the protocols can be applied to other intact animal, plant, and fungal tissues (.). As we show below, many factors must be taken into account in the choice of experimental parameters, there are no “best settings” that work for all tissues, in all cases.