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Moreover, we demonstrated cell sorting by the combination of gel-valves shown in Figure 10(b).
Furthermore, we demonstrated cell sorting by using two gel-valves fabricated near the branch of a microchannel on a chip.
The osteoblast cell adhesion test demonstrated cell spreading which is considered favourable for cell proliferation and differentiation.
Scanning electron microscopy (SEM) demonstrated cell attachment (average of 3.0×108 cells per bead) to the irregular surface.
Alamar blue and XTT cytotoxic assays demonstrated cell proliferation abilities and the non-cytotoxic effect of the R-SBgC.
Both aligned and nonaligned multilayered scaffolds demonstrated cell infiltration and ECM deposition through the full thickness of the scaffold after only 28 days of culture.
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In spite of the small size of the library used in this study, several peptides demonstrated cell-specific toxicity.
The MTX-loaded nanogels, unlike empty nanogels, lowered viability of HepG2 cells; the nanogels demonstrated cell-cycle arrest and apoptosis comparably higher than MTX as free drug that was shown to be through i) cellular uptake of the nanogels by clathrin-mediated transport and ii) endosomolytic activity of the nanogels in HepG2 cells.
The present study clearly demonstrated cell-cycle network and cell cycle regulation (Additional file 1: Figure S1F) in NFPAs.
Independently, Futaki and colleagues [ 19] demonstrated cell-surface exposure of PS upon incubation of cells with high concentrations of oligo-arginines.
We also demonstrated cell-type-specific disease phenotypes using patient-derived induced pluripotent stem cells (iPSCs) carrying ~100 % mutant m.5541C>T.
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