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Immunoaffinity Chromatography

  • Paul Cutler
Part of the Methods in Molecular Biology book series (MIMB, volume 244)

Abstract

The principle of immunoaffinity or immunoadsorption chromatography is based on the highly specific interaction of an antigen with its antibody (1). Immunoaffinity chromatography is a specialized form of affinity chromatography and, as such, utilizes an antibody or antibody fragment as a ligand immobilized onto a solid support matrix in a manner that retains its binding capacity. Although the technique includes the separation of antibodies using immobilized antigens (2, 3, 4), it is more commonly performed for the identification, quantification, or purification of antigens (see Note 1 and refs. 5 and 6). The crude extract is pumped through the column and the unbound material washed clear prior to elution of the retained antigen by alterations to the mobile-phase conditions that weaken the antibody-antigen interaction.

Keywords

Storage Buffer Cyanogen Bromide Elution Condition Cyanate Ester Immunoaffinity Chromatography 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Humana Press Inc., Totowa, NJ 2004

Authors and Affiliations

  • Paul Cutler
    • 1
  1. 1.Genomic and Proteomic Sciences, Medicines Research CenterGlaxoSmithKline PharmaceuticalsStevenageUK

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