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X-ray diffraction and transmission electron microscopy analyses demonstrated that ZnO nanoparticles with an average diameter of about 5 nm uniformly covered the graphene surfaces.
Flow cytometry and confocal microscopy analyses demonstrated that the pH-sensitive ILs were efficiently internalized by various CD33+ leukemic cell lines while limited interaction was found for liposomes decorated with an isotype-matched control antibody.
Small angle X-ray scattering and transmission electron microscopy analyses demonstrated that ordered nanostructures, from lamellar to 2-dimensional hexagonal columnar with a disordered intermediate morphology, were exhibited as a function of the amount of loaded silica nanoparticles.
Western blot experiments and immunofluorescence microscopy analyses demonstrated transfer of recombinase-dependent rep68 genes into target cells.
Electron microscopy analyses demonstrated the presence of vesicles, often aggregated, with a size (from 100 nm to 1 µm) compatible with MVs similarly purified from other cells (Fig. 4B) [23].
In addition, phase-contrast and electron microscopy analyses demonstrated that Caco-2/15 cells containing a low level of PTEN failed to acquire a fibroblastic or scattered morphology and retained their capacity to form some cell-cell contacts.
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Scanning electron microscopy and transmission electron microscopy analyses demonstrate that the microcapsules are ca. 550 nm in diameter and contain an empty hollow region surrounded by a ca. 40 nm thick polymer shell.
Petrographic photography and scanning electron microscopy (SEM) analyses demonstrated a uniform and homogeneous covering of the urea surface.
Further, electron microscopy and immunohistochemical analyses demonstrated that hMSC cultured under epidermis-specific conditions adopted a myofibroblastic phenotype and function, promoted in particular by air exposure.
Rigorous assessment of cell fraction purity by both microscopy and molecular analyses demonstrated that the CM fraction was almost completely clear of NM contamination, whereas the NM fraction routinely contained a low level of contaminating CM cells (see Materials and Methods, and supplementary material Fig. S2).
Transmission electron microscopy (TEM) analyses demonstrate that the BiOCl and BiVO4 phases distribute uniformly throughout the composite microspheres.
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