Sentence examples for binding assays were determined from inspiring English sources

EC50s for the binding assays were determined with non-linear regression.

The potency of peptides in vitro functional and binding assays was determined by the analysis of a concentration-response curves using non-linear regression analysis.

Methods: In 76 diabetic patients and 25 control subjects, a plasma level of IMA by manually performed, spectrophotometric Co II -albumin binding assay was determined.

Specifically, purified anti-CAIX scFvFc proteins were biotinylated and flow cytometric competitive binding assays were set up to determine whether presence of an unlabeled anti-CAIX scFvFc could block the binding of any biotinylated scFvFcs to the CAIX expressed on cell surface, the latter detected using streptavidin-FITC.

Nitrocellulose filter binding assays were used to determine GDP exchange by EF-Tu as previously described  [ 19, 20].

Therefore, with the use of 21-mer synthesized peptides, DR-peptide binding assays were performed to determine the pattern of collagen binding to DR4.

Competitive time-resolved fluorescence resonance energy transfer (TR-FRET) (Toth et al. 2012) binding assays were used to determine the affinity of DOSS for PPARγ (SelectScreen Service Life TechnologiesSelectScreen Service Life Technologies

Western blots, quantitative PCR and DNA binding assays were used to determine the activity of molecular markers of apoptosis in these animals.

Radioligand binding assays were performed to determine the potential of varying concentrations of soluble heparin and heparin oligosaccharides to compete with polymeric heparin or heparan sulphate to bind I-CXCL12.

Cellular binding assays were carried out to determine whether the mono-macrocyclic fluorescent compounds interact with the CXCR4 chemokine receptor.

Saturation radio-ligand binding assays were performed in HeLa cells to determine the binding capacity (Bmax) and equilibrium dissociation constant (Kd) values of rhTF.