Sentence examples for measuring the affinity from inspiring English sources

The NADH binding ability of LDHA was determined by measuring the affinity of LDHA to agarose-immobilized Cibacron Blue 3GA, which mimics NADH24.

Initial matrices are computed by maximizing the centered-kernel alignment (CKA) metric, measuring the affinity between projected samples and labels.

We tested the validity of the three sites by (i) using site-directed mutagenesis to introduce six amino acid changes designed to occlude them, (ii) producing the resulting tubulins recombinantly in Escherichia coli and (iii) measuring the affinity of the herbicides amiprophosmethyl and oryzalin for these proteins in comparison with wild-type tubulins by fluorescence quenching.

In essence, the first Kd is measuring the affinity of the protein for the RNA, which is relatively high, whereas the second Kd is measuring the affinity of the protein for an RNA protein complex.

By independently measuring the affinity of undamaged DNA and the overall equilibrium constant for εA-DNA binding, we can calculate a theoretical value for binding to the damaged site (Kfind = 14).

Concerning αvβ3, a radiometric cell-based assay has been widely used in measuring the affinity of αvβ3 targeting probes on a cellular level using U87-MG glioblastoma cells known to express αvβ3.

Binding to the low-affinity subunits was determined by measuring the affinities of IL-4, T13D and F82D bound to IL-4Rα IL-4Rα-13Rα1 and γc.

To confirm the results obtained by the NIR intact cell-based competitive binding assay measuring the affinities of 3 and 9 toward PSMA overexpressed on PC-3/PIP cells, a fluorescent protein-based assay was performed.

As ATPγS has the highest binding affinity among all ATP analogs, we then measured the affinity of ATPγS to purified KpBest mutants in MST.

UV-VIS electronic absorption spectra were employed to measure the affinity constants of drug/DNA binding using Scatchard analysis.

UV VIS electronic absorption spectral data were employed to measure the affinity constants of drug/DNA binding using Scatchard analysis.