Titlebook: Epitope Mapping Protocols; Glenn E. Morris Book 1996 Humana Press 1996

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Collar

外來

EVADE

爆米花

A Simple Solid-Phase Competition Assay with Labeled Antigen, the antigen is immobilized, and a radiolabeled antibody and competing unlabeled antibodies are mixed in solution (.) (.,.). Although this method facilitates separation of free from bound antibody, it possesses the problem of labeling all antibodies to be tested. Since the number of MAbs to be scree

mucous-membrane

mucous-membrane

Identifying Residues in Antigenic Determinants by Chemical Modification, proteolytic fragmentation, it played a major role in the pioneering efforts of Atassi and others to assign antigenic determinants on the surfaces of lysozyme and myoglobin (.,.). The principle of the method is that alteration of the structure of a key residue in an epitope by a chemical modificatio

燕麥

Epitope Mapping by Differential Chemical Modification of Antigens, in three-dimensional space. In the case of antibodies to native proteins, most or perhaps all epitopes are discontinuous (.). Because of the large size of a typical contact epitope in an antigen-antibody crystal, it is unlikely for an antibody to bind exclusively to a contiguous stretch of the poly

LAPSE

是他笨

Proteolytic Fragmentation for Epitope Mapping,dely used to provide antibodies with a defined specificity. One characteristic feature of this technology is that impure antigens can be used to produce monospecific antibodies that can be utilized to study the functional domains of protein molecules. In this chapter, the use of limited vs complete