首页> 外文期刊>FEBS Letters >Antigenic determinant and interspecies cross‐reactivity of a monoclonal antibody to poly(ADP‐ribose) synthetase
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Antigenic determinant and interspecies cross‐reactivity of a monoclonal antibody to poly(ADP‐ribose) synthetase

机译:单克隆抗体对聚(ADP-核糖)合成酶的抗原决定簇和种间交叉反应

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>A monoclonal antibody (1F4) was prepared against calf thymus poly(ADP-ribose) synthetase. It was classified as IgG1/κ and its antigenic determinant was localized on the 46 kDa portion of the enzyme molecule which contains the site for the binding of DNA. When calf thymus DNA-binding proteins were subjected to immunostaining after electrophoresis and transblotting to a nitrocellulose filter, the native enzyme (120 kDa) and its endogenous degradation products (80, 64 and 32 kDa) were detected. When the interspecies cross-reactivity was examined using DNA-binding proteins from 6 different sources, 1F4 reacted with the 120- and 32-kDa protein bands in HeLa cells, mouse testis and chicken liver as in the case of calf thymus. These results indicate that the antigenic structures ofpoly(ADP-ribose) synthetase and its degradation products are highly conserved in various animal cells.
机译:制备针对小牛胸腺聚(ADP-核糖)合成酶的单克隆抗体(1F4)。它被归类为IgG 1 /κ,其抗原决定簇位于包含DNA结合位点的酶分子的46 kDa部分。当小牛胸腺DNA结合蛋白在电泳后进行免疫染色并转移到硝酸纤维素滤膜上时,检测到天然酶(120 kDa)及其内源降解产物(80、64和32 kDa)。当使用来自6个不同来源的DNA结合蛋白检查种间交叉反应性时,与小牛胸腺一样,1F4与HeLa细胞,小鼠睾丸和鸡肝中的120kDa和32kDa蛋白带反应。这些结果表明聚(ADP-核糖)合成酶的抗原结构及其降解产物在各种动物细胞中高度保守。

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