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The capture range of the microwell can be designed for cells of various sizes.
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These molecules can be designed for cell-specific targeting by including adhesion ligands, receptor recognition ligands, or peptide-based antigens in their design, often in a multivalent display.
The NMR microprobes are designed for cell analysis and characterized using lipid vesicles as cell substitutes.
This method is designed for cell-centered Lagrangian schemes (GLACE [8,13,14], EUCCLHYD [25 29]).
The mapping technique is designed for cell centered control volume based algorithms and applicable to arbitrary polyhedral/polygonal mesh topologies.
To study selected therapeutic effects in defined experimental conditions, in vitro setups are designed for cell and tissue therapy.
Given that the DMS degradation activity of Alcaligenes sp. SY1 is inducible and the PT-degradation activity of Pseudomonas putida S-1 is constitutive, different strategies are designed for cell cultivation to obtain high VOSC removal rates of SCMI.
Here a simple cell-collecting kit based on size filtration and surface selection is designed for cell collection by packing surface modified silica gel particles into a pipet tip as a column.
Small protein fragments, also called peptides, are promising as drugs because they can be designed for very specific functions inside living cells.
The scheme is designed for polyhedral cells with nonplanar cell-faces.
WO3 bilayer electrodes composed of WO3 top and bottom layers are designed for photoelectrochemical cells (PECs).
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