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Macrophage activation was assayed by using fluorescence microscopy to visualize the phagocytosis of fluorescent beads by differentiated THP-1 macrophages following 30 min of lipid electrophile treatment and removal.
Fluorescently labeled cells were examined by using fluorescence microscopy.
Finally, by using fluorescence microscopy it was demonstrated that the PB2 is the photostable fluorescent probe and PB2 conjugate Concanavalin A exhibits a blue fluorescence.
Morphological differences on size and thickness of cell membranes were detected between the models studied by using fluorescence microscopy.
PLL/HA multilayer film formation was assessed by using fluorescence microscopy, contact angle measurements, cationic dye loading and confocal microscopy.
The silencing effect of M2-2 gene at the protein level was measured both qualitatively and quantitatively by using fluorescence microscopy and flow cytometry.
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For analysis of protein levels by immunoblotting, the homozygous rab11 mutant embryos (20 24 hrs) were selected by hand using fluorescence microscopy, using a GFP balancer chromosome to determine genotype.
Based on our finding of reduced levels of basal autophagy, we next investigated the clearance of dysfunctional mitochondria by autophagy using fluorescence microscopy on mitochondria and lysosomes.
This protocol yielded infection rates in excess of 80% (determined by visual assessment using fluorescence microscopy).
Infection-II was monitored by visualization GFP using fluorescence microscopy (Figure 9B).
(B) Assessment of the intracellular uptake of liposomes by A549 tumor cells using fluorescence microscopy.
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by using fluorescence microscope
by using immunoelectron microscopy
by using fluorescence imaging
by using fluorescence technique
by using fluorescence titration
by using electron microscopy
by using fluorescence analysis
by using fluorescence anisotropy
by using fluorescence recovery
by using fluorescence polarization
by using fluorescence detection
by using fluorescence resonance
by using fluorescence emission
by using fluorescence labeling
by using fluorescence spectrophotometry
by using fluorescence spectroscopy
by using fluorescence quenching
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