Sentence examples for binding assay based on from inspiring English sources
To evaluate the estrogenic activity of the aqueous extract from A. pilosa, the ability of A. pilosa to bind ERα and ERβ was assessed using a competitive binding assay based on fluorescence polarization.
The results were consistent with those determined by traditional methods, which confirmed the reliability of this competitive binding assay based on β-gal.
A novel competitive binding assay based on enzyme fragmentation complementation technology was established to screen the binding affinities of emerging chemicals for estrogen receptor (ER) α or β isoforms.
A new simplified binding assay based on nanoLC-linear ion trap ESI-MS for quantifying complexation of the B. mori pheromone-binding protein (BmPBP) with native (1) and prepared analogues was developed.
We have described a simple homogeneous binding assay based on luminescence resonance energy transfer.
To overcome these difficulties we combined a direct functional assay based on electrophysiology with a direct binding assay based on label-free tryptophan fluorescence.
The BODIPY-FL-labeled derivative 10 (see Scheme S2 in the Supporting Information) was designed as a tracer molecule for direct binding assays based on fluorescence polarization, and was found to bind to wild-type STAT5b with high affinity (Kd=0.86±0.08 μ m; Figure 2).
The design of homologous displacement ligand binding assays based on molecularly imprinted polymers (MIP) is discussed in terms of the MIP adsorption isotherm.
Competitive binding assays based on the lectin Concanavalin A (ConA) have displayed significant potential to serve in continuous glucose monitoring applications.
To confirm that these lectins are able to recognize the saccharidic chain of the saponins of H. forskali, we used a lectin-binding assay based on the technique developed by Smith [26] to detect cell surface glycolipids of human and bovine erythrocytes on thin layer chromatograms (TLC).
EGFR concentrations in crude membranes were analysed by a ligand-binding assay based on competition between I-EGF and unlabelled EGF (Santini et al, 1991).
