首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >A NEW METHOD FOR THE DETECTION OF PROTEOLYTIC ACTIVITY IN PSEUDOMONAS LUNDENSIS AFTER SODIUM DODECYL SULFATE-POLYACRYLAMIDE GEL ELECTROPHORESIS
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A NEW METHOD FOR THE DETECTION OF PROTEOLYTIC ACTIVITY IN PSEUDOMONAS LUNDENSIS AFTER SODIUM DODECYL SULFATE-POLYACRYLAMIDE GEL ELECTROPHORESIS

机译:十二烷基硫酸钠-聚丙烯酰胺凝胶电泳后检测假单胞菌蛋白水解活性的新方法

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A new method for the visualization of proteolytic activity in cell culture supernatant from Pseudomonas lundensis after sodium dodecyl sulfate (SDS) - gel electrophoresis is described. Following conventional electrophoresis, the gel is washed in a methanol-containing buffer to facilitate partial removal of SDS. After incubation with 0.5% casein the gel is stained for protein with Coomassie Brilliant Blue R-250. Bands with proteolytic activity appear as clear areas in the gel against a blue-stained background. Molecular weight standards electrophoresed in the same gel stain more intensely than the background and allow determination of the molecular weights of the proteolytic components. The sensitivity of post-electrophoretic reactivation in SDS-gels was determined using trypsin as standard. A slight modification of the technique allowed detection of proteolytic activity in nondenaturing and in isoelectric focusing gels. [References: 14]
机译:描述了一种可视化十二烷基硫酸钠(SDS)-凝胶电泳后隆起假单胞菌细胞培养上清液中蛋白水解活性的新方法。在常规电泳之后,将凝胶在含甲醇的缓冲液中洗涤,以促进SDS的部分去除。与0.5%酪蛋白孵育后,用考马斯亮蓝R-250将凝胶上的蛋白质染色。具有蛋白水解活性的条带在蓝色背景下的凝胶中显示为透明区域。在相同的凝胶染料上电泳的分子量标准品比背景电泳强度更高,并可以确定蛋白水解成分的分子量。使用胰蛋白酶作为标准品,测定SDS-凝胶中电泳后重新活化的敏感性。对该技术稍加修改即可检测非变性和等电聚焦凝胶中的蛋白水解活性。 [参考:14]

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