Sentence examples for binding studies in the from inspiring English sources

Binding studies in the absence of calcium revealed that all types of pectin were able to bind to cellulose and confirmed that binding of pectin with a high content of neutral sugar side chains (∼40%) was greater than that of homogalacturonan (less than 7% neutral sugars).

In addition, post-synaptic sensitivity to ACh may be increased on these neurons, as suggested by receptor binding studies in the pontine reticular formation of the narcoleptic canine, which found elevated mAChRs [45].

To prevent proteolytic cleavage of C5 by Bb, we performed these binding studies in the absence of FB and FD.

Next, we performed equilibrium DNA binding studies in the presence of concentrations of ADP and ATP-γ-S ranging from 0.5 to 2 mM.

We repeated our equilibrium binding studies in the presence of ADP and nonhydrolyzable ATP analogues to investigate the effect of the ATP hydrolysis cycle on DNA and nucleosome binding.

To explore this, we performed similar expression profiling and genome wide binding studies in the vertebral column of E12.5 wildtype and Sox9 null mice, to uncover its role independently, as well as decipher antagonistic and complementary co-regulatory roles between Sox9 and Bapx1, by comparing unique and shared target genes.

In addition to the thermodynamics of O2 binding studied in the above-mentioned works, it is crucial to understand the kinetics of this process.

This situation is somewhat similar to that of glycan-array binding studies, in which the probe that binds best on the glycan array does not necessarily bind the same glycan on the array as on cells and the identification of the glycan structure does not always result in the identification of the relevant biosynthetic enzyme.

Receptor binding studies in which the Ig-labelled polysaccharide-binding domains of dectin-1 were used to detect glucan binding have demonstrated that dectin-1 preferentially binds to the β-(1→3) part of the glucan, and that the minimal length required to allow binding to dectin-1 is 10 11 glucose residues [ 63].

In contrast to in vitro binding studies, in an in vivo setting, the concentration of a dedicated ligand to its target region is no longer constant, but changes over time after administration is often influenced by additional factors other than basic biomolecular ligand-receptor interactions.

While these studies appear to correlate MutL-ssDNA binding with MMR, all of the ssDNA binding studies in vitro were performed at non-physiological ionic strengths [6], [12].