Scanning and transmission electron microscopic analyses showed that the dispersed phase consist of mainly few layered graphene nanoflakes.
Immunofluorescence confocal microscopic analyses showed that a substantial population of endogenous Trak1 was localized to MitoTracker-labeled mitochondria in control cells (Fig. 1B).
Scanning electron microscopic analyses showed that fatigue crack growth is predominantly transgranular in vacuum (at temperature of interest) (see Figures 7a and b).
Immunodepletion, subcellular fractionation, and confocal microscopic analyses showed that the HGF-induced C/EBP DNA binding activity depended on nuclear translocation of C/EBPβ.
Transmission electron microscopic analyses showed that HPC moxifloxacin conjugates self-assembled into nanowires of ∼30 nm diameters while HEC moxifloxacin conjugates self-assembled into nanoparticles of 150 350 nm.
Microscopic analyses showed that TiO2 nanoparticles were nonspherical, irregular in shape, and <50 nm in size while WO3 nanoparticles were well distributed throughout TiO2 surface and were smaller (<20 nm) in size as compared to TiO2.
Gross and light microscopic analyses showed corneal decompensation and vascularization, peripheral anterior and posterior synechiae, iris thinning, significant changes in the iris pigmented layer, fibrous tissue on the anterior surface of the iris, and Soemmerring ring formation in the periphery of capsular bag remnants.
Our results based on microscopic analyses showed that Ehrlichia were contained in the filopodium of macrophages which were transported to neighboring cells.
Furthermore, electron microscopic analyses showed that tetherin appears to tether virions to each other as well as to the cells [1], [4].
This observation correlates with CFU determinations and fluorescence microscopic analyses shown in Figure 4. Despite the increased bacterial load, the intestinal barrier of LF82-infected nematodes appeared normal with intact terminal web and apical microvilli (Figure 5B).
