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免疫沉淀:变性裂解

Immunoprecipitation: denaturing lysis.

作者信息

Harlow Ed, Lane David

出版信息

CSH Protoc. 2006 Sep 1;2006(4):pdb.prot4534. doi: 10.1101/pdb.prot4534.

Abstract

INTRODUCTIONFor many sources of antigens, one useful method of lysis is to treat cells with harsh, denaturing solutions to release most of the protein antigens, as described here. The lysates are then diluted to reduce the denaturing conditions to levels that are suitable for the formation of antibody-antigen complexes. The resulting solution is precleared prior to immunoprecipitation. The major consideration in choosing this lysis method is that all noncovalent protein-protein interactions will be lost and that denaturation-sensitive epitopes will be destroyed. Therefore, this is not an appropriate method for many types of final assays, but it is a good method for quantitation of the antigen, careful identification of the polypeptide band recognized by the antibody, and display of denaturation-resistant epitopes.

摘要

引言

对于许多抗原来源,一种有用的裂解方法是用苛刻的变性溶液处理细胞,以释放大部分蛋白质抗原,如下所述。然后将裂解物稀释,以将变性条件降低到适合抗体 - 抗原复合物形成的水平。所得溶液在免疫沉淀之前进行预清除。选择这种裂解方法时的主要考虑因素是所有非共价蛋白质 - 蛋白质相互作用都将丧失,并且对变性敏感的表位将被破坏。因此,这不是许多类型最终检测的合适方法,但它是定量抗原、仔细鉴定抗体识别的多肽条带以及展示抗变性表位的好方法。

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