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Chromatography antibodies

Interfemn AJfa-2a (Recombinant). Interferon alfa-2a (recombinant). Roferon A. is expressed in ui AT. < /i system and purilled by using high-afllnily tiuiusc monoclonal antibody chromatography. The protein consists of 165 amino acids with a molecular mass of approximately 19.000 Da. and contains lysine at position 21 and hi.siidine at position 14. [Pg.180]

Another example of vims clearance is for IgM human antibodies derived from human B lymphocyte cell lines where the steps are precipitation, size exclusion using nucleases, and anion-exchange chromatography (24). A second sequence consists of cation-exchange, hydroxylapatite, and immunoaffinity chromatographies. Each three-step sequence utilizes steps based on different properties. The first sequence employs solubiUty, size, and anion selectivity the second sequence is based on cation selectivity, adsorption, and selective recognition based on an anti-u chain IgG (24). [Pg.45]

Immunoaffinity chromatography utilizes the high specificity of antigen—antibody interactions to achieve a separation. The procedure typically involves the binding, to a soHd phase, of a mouse monoclonal antibody which reacts either directly with the protein to be purified or with a closely associated protein which itself binds the product protein. The former approach has been appHed in the preparation of Factor VIII (43) and Factor IX (61) concentrates. The latter method has been used in the preparation of Factor VIII (42) by immobilization of a monoclonal antibody to von WiHebrand factor [109319-16-6] (62), a protein to which Factor VIII binds noncovalenfly. Further purification is necessary downstream of the immunoaffinity step to remove... [Pg.529]

Fig. 4. Example of antibody purification from animal or culture sources. In some cases, affinity chromatography may be used directly with the source... Fig. 4. Example of antibody purification from animal or culture sources. In some cases, affinity chromatography may be used directly with the source...
Most immunoassay kits and many commercial immunoassay analyzers are based on heterogenous EIA or FIA. These include an immunoassay system that uses FIA linked to radial partition chromatography of the antibody—antigen complex (39) a system that uses antibody-coated tubes for enzyme immunoassay of a variety of hormones and dmgs (40) and a system that uses either a sandwich or competitive FIA format to measure a variety of analytes (41). [Pg.28]

Sepharose (e.g. Sepharose CL and Bio-Gel A) is a bead form of agarose gel which is useful for the fractionation of high molecular weight substances, for molecular weight determinations of large molecules (molecular weight > 5000), and for the immobilisation of enzymes, antibodies, hormones and receptors usually for affinity chromatography applications. [Pg.23]

Fermentation broths are complex, aqueous mixtures of cells, comprising soluble extracellular, intracellular products and any unconverted substrate or unconvertible components. Recovery and extraction of product is important in bioprocess engineering. In particular separation is a useful technique it depends on product, its solubility, size of the process, and product value. Purification of high-value pharmaceutical products using chromatography such as hormones, antibody and enzymes is expensive and difficult to scale up.1 Tire necessary steps to follow a specific process depend on the nature of the product and the characteristics of the fermentation broth. There are a few steps for product recovery the following processes are discussed, which are considered as an alternative for product recovery from fermentation broth. [Pg.170]

Affinity chromatography, which is the binding of bio-molecules with the matrix bed, often used for antibodies and antigens... [Pg.188]

To allow all culture productiou to be coutrolled, a method for rapid analysis is required. Prior to development of an LC-MS method, the analysis was both complex and time-consuming, involving the purification of a relatively large amount of the antibody using affinity chromatography, enzymatic release, and subsequent derivatizafion of the oligosaccharides and their analysis by using capillary electrophoresis. [Pg.202]

Wrodnigg TM, Eder B (2001) The Amadori and Heyns Rearrangements Landmarks in the History of Carbohydrate Chemistry or Unrecognized Synthetic Opportunities 2/5 115 -175 Wyttenbach T, Bowers MT (2003) Gas-Phase Confirmations The Ion Mobility/Ion Chromatography Method. 225 201 -226 Yamaguchi H, Harada A (2003) Antibody Dendrimers. 228 237-258... [Pg.207]

Affinity chromatography (12) has become an important tool in the isolation of purified fractions of such substances as enzymes. Advantage is taken of specific interactions such as antigen-antibody interactions. One substance of the pair (e.g. antigen) is bonded to a support. When a mixture is passed through the column, the specific interaction retains the corresponding antibody relative to other substances. A change of mobile phase conditions then elutes the pure antibody. This method has a real potential for analysis of specific proteins in body fluids. [Pg.228]


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See also in sourсe #XX -- [ Pg.535 ]




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Affinity chromatography anti-carbohydrate antibodies

Affinity chromatography antibodies isolated

Affinity chromatography antibody—enzyme

Affinity chromatography, antibody purification

Affinity chromatography, utilizing antibodies

Antibodies affinity chromatography

Antibodies by affinity chromatography

Antibodies immunoaffinity chromatography

Antibody-enzyme conjugates chromatography

Chromatography antigen-antibody interactions

Hydrophobic interaction chromatography antibodies

Hydroxyapatite chromatography antibodies

Immunoaffinity chromatography antibody-antigen interaction

Metal interaction chromatography antibodies

Polyclonal antibodies affinity chromatography

Purification of Antibodies by Liquid Chromatography

Size exclusion chromatography antibodies

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