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Genetic manipulations or exogenous agents that induce myotube fragmentation can be observed using microscopy and provide a simple assay for candidate compounds that produce cellularization in mammalian muscles [21].
Such elements can be observed using microscopy (not shown).
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In addition to fluorescence imaging, individual QDs can be observed using electron microscopy, and correlated with fluorescence microscopy [18] [20].
Successful antibody immobilization could be observed using fluorescent microscopy.
Porphyrin 1 was poorly incorporated in vesicle membranes, but membrane-bound 1 could be observed using fluorescence microscopy.
Apoptosis in individual cells can be observed using fluorescence microscopy, and this can be coupled with detection of other markers such as green fluorescent protein reporter constructs [ 36].
The characteristic thickened capillary walls and double contours of the glomerular basement membrane (GBM) after periodic-acid-Schiff and/or silver staining can be observed using light microscopy.
The transfected cells were observed using fluorescence microscopy (Olympus, IX71), acquiring the images by confocal microscopy (Olympus, FV1000).
The signals were observed using fluorescence microscopy, and were evaluated by independent observers (Y.M. and T.S).
The signals were observed using fluorescence microscopy, and the FISH signals were evaluated by independent observers (TM and AK).
Pb2+ -stimulated phosphatidylserine exposure in CHO cells was observed using confocal microscopy (Fig. 2).
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