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用于检测镍结合蛋白的蛋白质印迹法。

Protein blotting method for detection of nickel-binding proteins.

作者信息

Lin S M, Hopfer S M, Brennan S M, Sunderman F W

机构信息

Department of Laboratory Medicine, University of Connecticut School of Medicine, Farmington 06032.

出版信息

Res Commun Chem Pathol Pharmacol. 1989 Sep;65(3):275-88.

PMID:2479061
Abstract

A technique is described for detection of nickel-binding proteins in tissue extracts by protein blotting and autoradiography. The proteins are separated by SDS-polyacrylamide gel electrophoresis and blotted onto a nitrocellulose membrane. The membrane is incubated with 63NiCl2 in a tris-HCl buffer that contains NaCl and CaCl2 to suppress non-specific Ni-binding. The membrane is washed to remove unbound 63Ni2+ and autoradiography is performed to visualize the 63Ni-binding proteins. The technique furnishes a sensitive means to detect 63Ni-binding proteins in tissue extracts, facilitating their isolation, characterization, and identification.

摘要

本文描述了一种通过蛋白质印迹法和放射自显影术检测组织提取物中镍结合蛋白的技术。蛋白质通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分离,然后转移到硝酸纤维素膜上。将膜在含有氯化钠和氯化钙的三羟甲基氨基甲烷-盐酸缓冲液中与63NiCl2一起孵育,以抑制非特异性镍结合。洗涤膜以去除未结合的63Ni2+,然后进行放射自显影以可视化63Ni结合蛋白。该技术为检测组织提取物中的63Ni结合蛋白提供了一种灵敏的方法,有助于对其进行分离、表征和鉴定。

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