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Predictive modeling and understanding of binding of organic molecule-decorated graphene is an essential prerequisite for tuning their electronic and magnetic properties.
Hydrophobicity and polymer porosity may enhance selective binding of organic high explosive analytes, which can be further enhanced in molecularly imprinted polymers [ 5, 35 ].
Recently, studies have been conducted on the binding of organic contaminants or toxins to HSA, for example, arazine, ochratoxin A, methyl parathion, arsenic, perfluorooctanoic acid, patulin, deoxynivalenol, and 2-mercaptobenzimidazole [ 10– 17].
Recently, studies have been conducted on the binding of organic contaminants or toxins to HSA, for example, Arazine, ochratoxin A, methyl parathion, arsenic, perfluorooctanoic acid and phthalate esters, deoxynivalenol, and 2-mercaptobenzimidazole [ 25– 325.
Binding of organic molecules (e.g., amelogenin (Kirkham et al. 2000)) at physiological solution pH appears to occur on the charged surface domains of apatite.
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The investigation describes interesting phenomena of simultaneous estimation of two metal ions by organizing the binding sites of organic receptors.
SOM, Al and Fe oxyhydroxides as well as SOM-Al/Fe oxyhydroxide complexes were identified as main binding partners of organic P at all sites.
FTIR is a convenient tool to study the binding patterns of organic linkers and Co2+.
In this context, the direct binding of functional organic conjugated molecules (stilbene derivative) onto the surface of monodisperse Fe3O4 magnetic nanoparticles has been studied.
The RKIP-PE complex is the only crystal-based structural evidence to date for the binding of an organic ion to the pocket.
The binding of the organic molecules to the receptor was evaluated on the basis of the interaction energy (Coulomb and van der Waals interactions) between receptor and ligand or cofactor peptide.
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