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Despite this, chloride ingress was greater at 38 °C; attributed to changes in the pore structure and the chloride binding capacities of the slag blends.
Here we constructed HA33/C mutants and evaluated the binding capacities of the individual sites through mucin-assay and isothermal titration calorimetry.
Through ratio optimization of the MUC1 and HER2 aptamers, the binding capacities of the Dual-SiNPs to both cell lines were maximized.
The binding capacities of the Fe2O3 nanomaterials with Cu2 + and Pb2 + were determined to be 19.61 mg/g and 47.62 mg/g, respectively.
The binding capacities of the particles were evaluated by equilibrium binding experiments.
Because of the extremely high binding capacities of the modified surfaces, the achieved yield of nucleic acids is practically unlimited, unlike that obtained through magnetic particle-based extraction, for example.
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Optimizations were done step-wise to investigate the binding capacity of the antibody towards the antigen in various blocking agents and target-unrelated proteins.
Variation in size distribution due to varying water binding capacity of the MCC samples was observed.
The nutrient anion binding capacity of the gels was studied as a function of various processing parameters.
Binding capacity of the lymphocytes was evaluated using human umbilical cord vein endothelial cells (HUVECs) as the binding matrix.
The order of lipopeptide binding capacity of the metals was Fe2+ > Ca2+ > Mg2+, with Fe2+ significantly influencing the foam stability.
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