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We have investigated and carried out detailed analysis to design high performance affinity biosensor by exploiting the unique optical properties of chalcogenide glass and graphene.
high performance affinity chromatography.
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The degeneracy of antisense peptides was studied by high-performance affinity chromatography.
A number of tools based on high-performance affinity separations have been developed for studying drug-protein interactions.
A system based on high-performance affinity chromatography was developed for characterizing the binding, elution and regeneration kinetics of immobilized antibodies and immunoaffinity supports.
The affinity inhibitor of fusion peptide of influenza A virus has been studied using a combination of high-performance affinity chromatography (HPAC) and combinatorial peptide libraries.
High-performance affinity chromatography (HPAC) was used in a variety of formats to examine multi-site interactions between glimepiride, a third-generation sulfonylurea drug, and normal or in vitro glycated forms of the transport protein human serum albumin (HSA).
High-performance affinity chromatography (HPAC) is another technique that has been used to characterize these interactions.
The use of pressure-resistant solid supports is often referred to as the defining advantage of high-performance affinity chromatography over conventional affinity chromatography, and was a starting point for rapid expansion of the number of applications reported in this field [ 8].
Specific high-performance affinity-chromatographic separations can be optimized by rational selection of chiral columns, the characteristics of which are provided by QSRR.
Kullolli et al. recently developed a High Performance Multi-Lectin Affinity Chromatography (HP-MLAC) composed of lectins ConA, JAC, and WGA.
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