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University of Nebraska - Lincoln

David Hage Publications

Immunoaffinity chromatography

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Full-Text Articles in Physical Sciences and Mathematics

Affinity Chromatography: A Historical Perspective, David S. Hage, Ryan E. Matsuda Jan 2015

Affinity Chromatography: A Historical Perspective, David S. Hage, Ryan E. Matsuda

David Hage Publications

Affinity chromatography is one of the most selective and versatile forms of liquid chromatography for the separation or analysis of chemicals in complex mixtures. This method makes use of a biologically related agent as the stationary phase, which provides an affinity column with the ability to bind selectively and reversibly to a given target in a sample. This review examines the early work in this method and various developments that have lead to the current status of this technique. The general principles of affinity chromatography are briefly described as part of this discussion. Past and recent efforts in the generation …


Affinity Monolith Chromatography: A Review Of Principles And Recent Analytical Applications, Erika L. Pfaunmiller, Marie Laura Paulemond, Courtney M. Dupper, David S. Hage Mar 2013

Affinity Monolith Chromatography: A Review Of Principles And Recent Analytical Applications, Erika L. Pfaunmiller, Marie Laura Paulemond, Courtney M. Dupper, David S. Hage

David Hage Publications

Affinity monolith chromatography (AMC) is a type of liquid chromatography that uses a monolithic support and a biologically-related binding agent as a stationary phase. AMC is a powerful method for the selective separation, analysis or studies of specific target compounds in a sample. This review discusses the basic principles of AMC and recent developments or applications of this method, with particular emphasis being given to work that has appeared in the last five years. Various materials that have been used to prepare columns for AMC are examined, including organic monoliths, silica monoliths, agarose monoliths and cryogels. These supports have been …


Biointeraction Analysis By High-Performance Affinity Chromatography: Kinetic Studies Of Immobilized Antibodies, Mary Anne Nelson, Annette C. Moser, David S. Hage Jan 2010

Biointeraction Analysis By High-Performance Affinity Chromatography: Kinetic Studies Of Immobilized Antibodies, Mary Anne Nelson, Annette C. Moser, David S. Hage

David Hage Publications

A system based on high-performance affinity chromatography was developed for characterizing the binding, elution and regeneration kinetics of immobilized antibodies and immunoaffinity supports. This information was provided by using a combination of frontal analysis, split-peak analysis and peak decay analysis to determine the rate constants for antibody–antigen interactions under typical sample application and elution conditions. This technique was tested using immunoaffinity supports that contained monoclonal antibodies for 2,4-dichlorophenoxyacetic acid (2,4-D). Association equilibrium constants measured by frontal analysis for 2,4-D and related compounds with the immobilized antibodies were 1.7–12 × 106 M−1 at pH 7.0 and 25 °C. Splitpeak …