Third, using confocal microscopy it was found that GdBN co-localise with lysosomes but not with mitochondria.
From scanning electron microscopy, it was found that connection between MgB2 grains and voids strongly depend on the growth temperature.
After examination under SEM and light microscopy, it was revealed that the number of cells decreased in the presence of pure Mg, Mg10Gd and WE43.
By means of immuno-electron microscopy, it was shown that MMP-9 associates with hippocampal dendritic spines bearing asymmetrical (excitatory) synapses.
By fluorescence microscopy, it was observed that the nanoparticles were not located homogeneously on the cells and on the membrane (Figure 5).
Using electron microscopy it was confirmed that bundles of nanowires were present, whose size increases with increasing concentrations.
Additionally, through phase-contrast and scanning electronic microscopy, it was shown that aging TSCs were large, flat and heterogeneous in morphologies while young TSCs were uniformly elongated.
Through Raman spectroscopy and electron microscopy it was confirmed the carbon-carbon contact, due to the tribolayer formation on the wear scars of the coating and pin.
Combining biophysical tools (ellipsometry, tensiometry and atomic force microscopy), it was evidenced that rDGL partitions toward liquid expanded phase and at phase boundaries.
Using scanning electron microscopy, it was established that the morphology of pores located on the surface and within the porous scaffolds showed equally good pore interconnectivity with zein.
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.
