Sentence examples similar to microscopy determined that from inspiring English sources

Transmission electron microscopy (TEM) and atomic force microscopy (AFM) determined that a 1-D fibrillar structure was obtained when the hard segment featured ureas whereas a 3-D structure was achieved when a combination of urea and urethane groups was used, giving rise to enhanced elongation properties.

By polarized optical microscopy, we determined that the anisotropic texture of the fibers was indicative of parallel alignment of the molecular chains to the fiber axis.

Wide-angle X-ray diffraction (WAXD) and transmission electron microscopy (TEM) determined that the compounded pellets and the blown film PLA/MLS nanocomposites were intercalated.

Furthermore, cross-sectional transmission electron microscopy techniques determined that the reduced coefficient of friction at T ~ 750 °C was primarily the result of the formation of a lubricious AgTaO3 phase that reconstructs during the wear process into a mechanically mixed layer of AgTaO3, Ta2O5, and Ag nanoparticles.

Using light microscopy, we determined that the USA300 strain LAC was ingested rapidly by phagocytic leukocytes largely neutrophils in human blood (Fig. 1A).

By immunofluorescence microscopy, we determined that compared to age-matched prostate tissues, C1q is significantly downregulated in benign prostatic hyperplasia (BPH) and prostate cancer (Figs. 7A and 7B; 100× magnification).

Using GFP markers and electron microscopy, they determined that the number of new GABAergic synapses increases by less than 30%, while each existing synapse increases in size by at least threefold.

By histology, immunofluorescence, and electron microscopy we determined that the collagen matrix is abundant and disorganized, smooth muscle cell orientation is disordered, and inflammatory infiltrates are significantly increased, and are comprised of macrophages, T cells and, to a lesser extent, B cells.

Using phase contrast and immunofluorescence microscopy, we determined that only two cell lines underwent EMT.

Using confocal microscopy, we determined that a small amount of CB1 receptors are present on the PSCs. Figure 1B shows six confocal images collected at 0.5-µm intervals.

Using mono-specific anti-BACE1 antibodies, we performed immunofluorescence confocal microscopy and determined that BACE1 is highly localized within synaptophysin-positive puncta in large mossy fiber terminals (giant boutons) of CA3.