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Cell surface engineering is an expanding field and whilst extensive research has been performed decorating cell surfaces with biomolecules, the engineering of cell surfaces with particles has been a largely unexploited area.
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A KEGG pathway analysis was performed in each cell line.
Experiments were performed at ∼70% cell confluence.
d5CXCR4+ sorting was performed on live cells.
Each experiment was performed on 1 2.106 cells.
Analyses were performed on freshly collected cells.
The experiments were performed using phospholipid vesicles decorated with DBCs with a hydrodynamic diameter of [196±20] nm, as determined by dynamic light scattering analysis.
To identify the immune cell subset that conferred CD4-down modulation of BT-061 decorated T cells, co-incubation experiments were performed either with PBMC depleted of selected immune cell subsets, or with the respective MACS-enriched immune cell subsets.
A similar study was performed, in which activated graphene was decorated with 5 nm LiFePO4 for a cathode in LIBs [135].
Cell counts were performed manually.
Cell counts were performed using ImageJ.
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