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Saccharide binding studies were conducted by UV vis, fluorescent, and circular dichroism (CD) spectroscopies.
Saccharide binding studies were conducted by UV vis, fluorescence, and circular dichroism (CD) spectroscopies.
In addition, binding studies were conducted using [125I]-BH-CCK-8S [125I]-BH-CCK-8S [125I]-BH-CCK-8S [125I]-BH-CCK-8S
Binding studies were conducted to determine the dissociation constant of the pair A BX, which was found to be KD∼10−8 m.
Binding studies were conducted and the anxious phenotype was found to be present with modifications caused by the BZ antagonist [3H]flumazenil and the 5-HT1B receptor agonist [I125]cyanolopindolol [25], [25].
Both in vitro and in vivo DNA binding studies were conducted (Gardner et al. 1997; NTP 2000).
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The ligand-binding studies were conducted and validated at NCTR National Center for Toxicological Researchh, Jefferson, USA).
Cell-binding studies were conducted on adherent Chinese hamster ovary cells (CHO-K1) and CHO-K1 cells stably expressing the human adenosine A3 receptor (CHO-K1-hA3R).
Kinetic real-time cell-binding studies were conducted on CHO-K1-hA3R cells with [125I]-AB-MECA at ambient temperature with LigandTracer® Grey.
To attest our prediction, G-quadruplex binding study was conducted between two salt forms of TMPyP4, i.e., tetratosylate and tetrachloride, by using ESI-QTOF-MS, UV-melting measurement, and molecular modeling studies.
However, no formal protein-binding study was conducted, and thus it was not possible to determine the influence of protein-binding on the pharmacokinetic profile of LY2457546.
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