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Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

机译:蛋白质从聚丙烯酰胺凝胶电泳转移到硝酸纤维素膜上的方法和一些应用。

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摘要

A method has been devised for the electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets. The method results in quantitative transfer of ribosomal proteins from gels containing urea. For sodium dodecyl sulfate gels, the original band pattern was obtained with no loss of resolution, but the transfer was not quantitative. The method allows detection of proteins by autoradiography and is simpler than conventional procedures. The immobilized proteins were detectable by immunological procedures. All additional binding capacity on the nitrocellulose was blocked with excess protein; then a specific antibody was bound and, finally, a second antibody directed against the first antibody. The second antibody was either radioactively labeled or conjugated to fluorescein or to peroxidase. The specific protein was then detected by either autoradiography, under UV light, or by the peroxidase reaction product, respectively. In the latter case, as little as 100 pg of protein was clearly detectable. It is anticipated that the procedure will be applicable to analysis of a wide variety of proteins with specific reactions or ligands.
机译:已经设计出一种方法,用于将蛋白质从聚丙烯酰胺凝胶电泳转移到硝化纤维素薄片上。该方法导致核糖体蛋白从含尿素的凝胶中定量转移。对于十二烷基硫酸钠凝胶,获得了原始的带状图案,没有分辨率的损失,但是转移不是定量的。该方法允许通过放射自显影检测蛋白质,并且比常规方法更简单。固定的蛋白可通过免疫程序检测。硝酸纤维素上所有额外的结合能力都被过量的蛋白质所阻断;然后结合特异性抗体,最后结合针对第一抗体的第二抗体。第二抗体被放射性标记或与荧光素或过氧化物酶偶联。然后通过放射自显影,在紫外线下或通过过氧化物酶反应产物分别检测特异性蛋白质。在后一种情况下,显然可以检测到低至100 pg的蛋白质。预期该程序将适用于分析具有特定反应或配体的多种蛋白质。

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