Actin polymerization was detected using fluorescent phalloidin and analyzed by confocal microscopy and fluorescence activated cell sorting analysis.
3D cell migration and cell transfection were monitored through time-lapse video microscopy and fluorescence microscopy.
Results were confirmed by scanning electrode microscopy and fluorescence microscopy after live/dead cell staining.
The membranes were characterized by X-ray photoelectron spectroscopy, scanning electron microscopy and fluorescence microscopy.
Transmission electron microscopy and fluorescence microscopy confirmed a significant uptake of AANTs by RAW 264.7 cells and breast cancer cells.
As demonstrated by electron microscopy and fluorescence in situ hybridization, abundant bacteria are present within the calcium bodies.
The enzyme lipid LB films were then characterized with PM-IRRAS, atomic force microscopy and fluorescence spectroscopy.
The microspheres were loaded with rhodamine-B-dextran and degradation was studied with confocal microscopy and fluorescence spectroscopy.
Micelle nanoparticles' (MNPs) formation of this amphiphilic copolymer in aqueous solution was studied by dynamic light scattering, transmission electron microscopy and fluorescence technique.
Spectrofluorometric analyses, confocal microscopy and fluorescence cell sorting revealed different rates and extent of multifunctional conjugate(s) internalization in the two cell types.
Scanning electron microscopy and fluorescence studies were employed to investigate the changes in macrophage morphology and adhesive properties, while MTT assay was used to quantify cell proliferation.
