Sentence examples for binding affinity of each from inspiring English sources

Exact(26)

The binding affinity of each nanoconjugates for TNT detection by using Langmuir adsorption methods has also been investigated.

All five NK1 antagonists exhibited similar binding to human and gerbil NK1 receptors; however, the binding affinity of each antagonist was greatly reduced at the rat NK1 receptor, compared with gerbil and human.

Membrane orientation of the reconstructed bR-PLs or FoF1-PLs was assessed by observing the binding affinity of each protein component to Ni-NTA Magnetic Beads, and 41.3 mM of lipid mixture (SoyPC extract/cholesterol with the molar ratio of 70 30) was reconstituted with either FoF1 or bR at the protein concentration of 0.2 µM.

Then, a single-point Kd calculation method (Qin et al. 2015) was employed to estimate binding affinity of each ligand to the receptor (Table 1).

Well consistent with the above theoretical analysis, our result further suggested that the targeting specificity of the nanoscaled drug delivery systems for a particular cell type can be enhanced by the weaker binding affinity of each individual receptor-ligand pair.

To determine the binding affinity of each selected or recombinant clone, the apparent Kd of the individual clones were assessed by phage ELISA.

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Similar(34)

Comparing the types of ligands reveals that the binding affinities of each peptide for the two adsorbents are similar.

The overall peptide binding preferences for the DR1201 allele were deduced by incubating these peptides in competition with the reference H1MP40 54 to determine the relative binding affinities of each to recombinant DR1201 protein.

We then measured the binding affinities of each construct using a bead-based fluorescence assay.

If we were to investigate two or more transcription factor binding motifs using this approach, it would be necessary to know more about the relative binding affinities of each, or to assume equal affinity, for better or worse.

While none of the analogs tested were as potent or selective as largazole, the Zn2+-binding affinity of each ZBG correlated with HDAC inhibition and cytotoxicity.

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