Justus C W, Müller H P, Simon M M, Kramer M D
MPG Klinische Forschungsgruppe für Blutgerinnung und Thrombose, Giessen, F.R.G.
J Immunol Methods. 1990 Jan 24;126(1):103-8. doi: 10.1016/0022-1759(90)90017-p.
An ELISA test system has been developed for the quantification of the two distinct forms of the proteinase inhibitor alpha 2-macroglobulin (alpha 2M): (i) free alpha 2M (functionally active), which is the electrophoretically slow form (alpha 2 MS), and (ii) the alpha 2 M-proteinase complex (functionally inactive), which is the electrophoretically fast form of alpha 2 M (alpha 2 MF). Discrimination between the two types of alpha 2 M was achieved using extracts of the two independent streptococcal strains, M1 and Sc1, which express receptors for alpha 2 MS and alpha 2 MF, respectively, in combination with a monoclonal antibody specific for alpha 2 M. The assay system described is easy and reliable and permits quantitation of alpha 2 MS and alpha 2 MF in complex biological samples such as plasma and cutaneous suction blister fluid.
已开发出一种酶联免疫吸附测定(ELISA)测试系统,用于定量蛋白酶抑制剂α2-巨球蛋白(α2M)的两种不同形式:(i)游离α2M(功能活跃),即电泳慢型(α2MS),以及(ii)α2M-蛋白酶复合物(功能无活性),即α2M的电泳快型(α2MF)。使用两种独立的链球菌菌株M1和Sc1的提取物实现了对两种类型α2M的区分,这两种菌株分别表达α2MS和α2MF的受体,并结合了对α2M特异的单克隆抗体。所描述的测定系统简便可靠,可对血浆和皮肤吸引疱液等复杂生物样品中的α2MS和α2MF进行定量。