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- W2014227890 abstract "This chapter discusses the use of bioaffinity chromatography (BAC) in the isolation, determination, or removal of biologically active substances. The preparation of specific sorbents utilizing the exceptional properties of biologically active substances to form specific and reversible complexes has enormously facilitated the isolation of a number of antibodies, antigens and haptens, cells and cell organelles, cofactors and vitamins, and glycoproteins and saccharides. The different conditions applied during BAC depend on the nature of the substances to be isolated. In high-performance liquid bioaffinity chromatography (HPLBAC), the biospecificity of BAC is combined with a high-performance (pressure) technology based on the rigid particles of a uniform small size (high-performance liquid chromatography, HPLC). The separation times in HPLBAC are short (minutes) compared to hours for traditional, soft-gel BAC. Moreover, HPLBAC users have at their disposal a wide selection of HPLC equipment, including high-speed pumps, sophisticated injection units, detectors of various kinds, auto-sampling devices, and data-handling capabilities. This enables the users to fine-tune the separation process conveniently and promote higher productivity." @default.
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- W2014227890 title "Purification of the fucose-binding lectin from Ulex europeus by affinity chromatography on new synthetic copolymers" @default.
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- W2014227890 doi "https://doi.org/10.1016/s0300-9084(78)80754-8" @default.
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