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The results of isotherm adsorption showed that the binding capacity of human immunoglobulin G (IgG) was high at pH 78 and low at pH 45.
Studies are needed in which the pathogen binding capacity of human geophagic clays is evaluated, i.e. viruses, bacteria.
In this study we demonstrate that the DC-SIGN binding capacity of human milk from different mothers is highly variable.
To test this hypothesis, we determined the BSSL protein size and DC-SIGN binding capacity of human milk for 17 mothers from the Netherlands.
ABiC was developed to assess the binding site II–specific binding capacity of human serum albumin, the binding site of, for example, bile acids [ 38].
In contrast, supernatants of triplicate productions of each scFv-Fc antibody expression vector were combined prior purification which resulted in a lower recovery rate of about 50% probably due to the lower efficacy of the 1 mL Bio-Scale Mini UNOsphere SUPrA Cartridges (binding capacity of human IgG1 ca. 20 mg) when applying more than 10 mg scFv-Fc antibody.
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Similar decoration of T cells from both species with TGN1412 indicated similar binding capacities of human and non-human primate CD28 to the antibody.
The CP-binding capacity of human, murine and scFv antibodies was measured by ELISA.
We hypothesized that the DC-SIGN binding capacity of BSSL and human milk is correlated with the BSSL protein size.
Removal of any one of the P, D, T or R led to loss of the binding capacity of either the human or the murine antibody indicating their specificity for the same epitope.
Automated membrane screenings allowed the identification of optimal VLP binding conditions yielding a dynamic binding capacity of 5.7 mg/mL for human B19 parvovirus-like particles derived from Spodoptera frugiperda Sf9 insect cells.
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