Sentence examples for binding to monitor from inspiring English sources

In Figure 1, we used I-PFO* binding to monitor delivery to the PM, and we used ACAT-mediated cholesterol esterification as an indirect monitor of cholesterol delivery to the ER.

The detailed characterizations of ABAleons demonstrate the utility of ABAleon2.1 (K′d ∼ 100 nM) and ABAleon2.15 (K′d ∼ 600 nM), which exhibit a sufficient ABA-specificity and dynamic range (9 10 %) upon ABA binding to monitor instantaneous ABA-induced or environmentally-triggered ABA concentration changes.

Flow cytometry was used in all the binding assays to monitor the process and enrichment of the selection pools.

To confirm these data and to set up a quantitative binding assay to monitor the interaction of KLHL3 with the motif, we expressed and purified either full-length KLHL3 or the isolated C-terminal Kelch domain (residues 290 587) and used fluorescence polarization to study the interaction of a 19-residue peptide encompassing the conserved acidic degron of WNK4 (residues 549 567: GPPSVFPPEPEEPEADQHQ).

Here, alternative methods are used to characterize the structural properties of the RAGE-ligand binding domain and to monitor the binding of a series of truncated variants of Aβ.

To determine the optimal synthesis parameters for on-array aptamer binding experiments, arrays were used to monitor binding of streptavidin to aptamer sequences on the array after the quality check by QC hybridization.

WHEN America's International Religious Freedom Act (IRFA) entered force in 1998, binding the administration to monitor liberty of conscience across the world and call out violators, the law's instigators assumed that tyrannical states were the main perpetrators of religious persecution.

Here we describe an LRET binding assay used to monitor the interaction of E. coli σ70 and σ32 with core RNA polymerase along with the controls to verify the system.

Alternatively, GFP variants have been conjugated to the N- and C-termini of periplasmic-binding proteins in order to monitor ligand binding by fluorescence energy transfer (Fehr et al. 2002; Fehr et al. 2003; Schultz and Moini 2003).

The use of the AuNP-FAM energy transfer pair allows the binding affinity to be measured and the change in distance following ATP binding to be monitored using nanometal surface energy transfer techniques.

To investigate how ATP binding and hydrolysis affect RNA binding, we used fluorescence anisotropy to monitor RIG-I binding to a FAM-labeled 10-mer RNA hairpin alone or when bound to various nucleotides and nucleotide analogs.