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Capturing pixel on pixel
registered multiple wavelength images, either
sequentially or simultaneously depending on
experiment conditions, records the perfect data for
co-localisation studies. The ability to optically
superimpose the confocal images on bright field,
phase contrast and other conventional microscope
images is also a powerful tool to identify the
location of fluorescent sources in the confocal
section with respect to the underlying structures,
without necessarily having multiple fluorescent
stains.
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