Sentence examples for binding tests using an from inspiring English sources

Twenty putative ligands that evoke an electrophysiological antennal response [5], [6], [8], [46], [47], were used in ligand binding tests using an established fluorescence-quenching assay [9] adapted by Inscent Inc. (Irvine, CA) for high throughput.

To determine if mPR α protein in MB231Br cells is translocated to the membrane compartment, we performed in vitro binding tests using a cell impermeable P4 conjugate (P4-BSA-FITC).

One scaffold was synthesized and inhibitory binding tested using a fluorogenic ACE assay.

However, this interaction was not detected in our in vitro binding test using size exclusion chromatography.

We studied the nonfouling properties of these PMAP/TiO2/quartz surfaces with the nonspecific binding test using 100 nM Cy3 14 nt ssDNA (5 min incubation).

Samples found to be positive for brodalumab-binding antibodies were further tested using an internally validated, cell-based bioassay to determine if the antibodies were able to neutralize the activity of brodalumab.

After elution, phages from each panning round were amplified and recovered, their binding efficiencies were tested using a phage ELISA as described in Materials and Methods.

Furthermore, nuclear extracts harvested from IVD cells treated with fHAs demonstrated no significant increase in NF-κB (p65) DNA binding activity when tested using a specific transcription factor assay.

The HAc hypothesis was tested using an integrative TF binding site (TFBS) prediction framework and using an approach designed to estimate the performance that the prediction model would have on a novel TF for which only a binding site motif is available.

The in vivo HER2-binding specificity was also tested using a group of animals that were bearing HER2-negative U251 tumors.

To address this, predictions from in silico ligand-RAR docking calculations and molecular dynamics simulations for a small library of stable, synthetic retinoids (designated GZ series) containing a central thiazole linker structure and different hydrophobic region substituents, were tested using a ligand binding assay and a range of cellular biological assays.