Examination by electron microscopy revealed the complexes in clathrin-coated pits.
Veins were explanted and prepared for histologic examination, scanning electron microscopy, and functional studies in organ chambers.
In total, 200 faecal samples from randomly selected healthy cats (148) and cats with diarrhoea (52) were tested and compared with the results of examination by electron microscopy.
Examination by electron microscopy revealed that the CNTs grown under optimum conditions had diameters of 11.8 ± 1.9 nm (average diameter ± standard deviation) and possessed an open-tip morphology.
Based on histological examination, scanning electron microscopy (SEM) and atomic force microscope (AFM), Ag-col was composed of the D-periodic cross-striated collagen fibrils and thick collagen fiber bundles with uneven diameters and non-orientated arrangement.
However, FIB technology overcomes many of these difficulties allowing microstructural characterization to be performed both by cross-sectioning and imaging coatings and by specimen preparation of electron transparent cross-sections for subsequent examination by electron microscopy.
Several lineages previously classified within the "Gymnodiniales" have been removed from this subgroup upon closer examination with electron microscopy and molecular phylogenetic analyses [37].
A closer examination with electron microscopy and immunocytochemistry revealed that Aβ is present in diverse subcellular organelles in neuronally differentiated P19 cells, including early endosomes, trans-Golgi network, rough endoplasmic reticulum, outer mitochondrial membrane, and nuclear envelope[9].
For examination by electron microscopy, nuclei isolated in polymer solution were pelleted (5000 g, 30 min in Ficoll and dextran or 700 g, 10 min in PEG) and suspended in the same polymer solution; nuclei isolated in "physiological buffer" [5] were pelleted (200 g,10 min) and resuspended in the same buffer.
HPE – Histo-pathological examination, EM – Electron Microscopy.
