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Saturation binding studies were carried out to analyse the in vitro binding properties of the diabody.
The anion binding studies were carried out using various techniques including electrochemistry, fluorescence and 1H NMR spectroscopy.
Cell viability assay was done by MTT-assay while the binding studies were carried out using fluorescence spectroscopy, circular diachroism, molecular modelling and computational analysis.
The anion binding studies were carried out using various techniques including electrochemistry (CV and SWV), UV vis and 1H NMR spectroscopy.
To provide a more concrete support for such a model, ACTD equilibrium binding studies were carried out and the results are reported herein on oligomers of sequence motifs d TGTCTnG) and d TGTnGTC).
In vitro binding studies were carried out with [125I]IMPY and [3H]SB-13 in homogenates prepared from postmortem samples of affected cortex and cerebellum of pathologically confirmed AD patients and age-matched controls.
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Docking and binding energy studies were carried out to reveal details regarding the favorable interactions between the scaffolds of these new inhibitors and the active sites of the investigated CA isoforms.
Experimental DNA binding and computational docking studies were carried out to identify the biological targets of 1 12.
In order to elucidate structural and functional relevance in terms of ligand binding and specificity, docking studies were carried out using different programs.
In order to better rationalize the action and the binding mode of these compounds, docking studies were carried out.
Molecular docking studies were carried out to highlight binding site interactions.
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