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In the case of laboratory c-Si cells, the importance of the passivation of both cell surfaces is well recognized.
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The assembly of Atx on cell surfaces is not well understood.
Together, these data suggest that Glut3 trafficking to cell surfaces is impaired in HD140Q/140Q primary neurons.
Cell surfaces are covered with structures between 50 nm and 20 µm.
Generally, cell surfaces are charged negatively.
The bacterial attachment to the cell surfaces was evaluated microscopically.
At high magnification philophodia surrounding cell surfaces were clearly visible.
Since the cell surfaces are negatively charged, cells attach to the PLL via ionic bonding.
The presence of membrane-anchored tM2e on cell surfaces was determined by a cell surface immune-assay.
The binding activity of CF172 for CXCR4 expressed on cell surfaces was examined by flow cytometry.
Cell surfaces were segmented and divided into cytoplasmic and nuclear regions according to manufacturer standard proceedings.
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