Sentence examples for binding analysis revealed that from inspiring English sources
Saturation binding analysis revealed that chronic treatment with T14 or T30, but not T15, increased the number of available receptor binding sites and altered receptor affinity for ligands.
The binding analysis revealed that in addition to CXCR2-CTD, CXCR1, CXCR3-CTDs bound LASP-1 directly, but the CXCR4-CTD failed to bind LASP-1 (Figure 4A).
In vitro binding analysis revealed that TFE, TOY3, or TOY8 could interact not only with MD-2 but also with LPS/MD-2 complex (Figure 2 and Figure S1).
In vitro liver tissue binding analysis revealed that IFN-CSP specific targeting to liver tissue [ 13].
In Petunia, in vitro binding analysis revealed that the conserved QALGGH motif played a critical role in DNA binding activity.
Parallel Western blot assay and radioligand binding analysis revealed that Rh1 could increase the expression and binding of GR.
The binding analysis reveals that the pyrimidine derivatives are anchored in TM2, 3, 5, 6 and 7 of A2A AR by the aromatic stacking and hydrogen bonding interactions.
Radioactive ligand-binding analysis revealed that NAc DAT protein expression was indeed increased in pmch−/− rats, both in the nucleus accumbens core (AcbCo; 118±6%) and in the AcbSh (123±5%; Fig. 6B).
While both zebrafish IGFBP-1a and -1b are capable of IGF binding, binding kinetics analysis revealed that the two proteins have very different IGF binding properties.
Transcription factor binding site analysis revealed that, out of the changed genes that did not contain a PPRE, 27% contained a binding site for at least one of the other five selected transcription factors These genes appear not to be regulated by PPARα directly, but indirectly, via these other transcription factors, a mechanism which has been suggested before [ 27, 28].
Molecular modeling analysis of the potent compounds provided further insight into the biological properties where detailed binding mode analysis revealed that the conjugates (8a r) were found stabilized in the active site of the enzymes through the development of a number of interactions with catalytic residues.
