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首页> 外文期刊>Proteomics >Purification of biotinylated proteins on streptavidin resin: A protocol for quantitative elution
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Purification of biotinylated proteins on streptavidin resin: A protocol for quantitative elution

机译:链霉亲和素树脂上生物素化蛋白的纯化:定量洗脱方案

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摘要

The interaction between streptavidin and biotin is one of the most widely used tools in chemistry and biology. However, the release of biotinylated proteins from streptavidin resins remains a major problem, due to the extraordinary stability of this complex. We present a new protocol for the quantitative elution of biotinylated proteins from streptavidin Sepharose, featuring harsh elution conditions and competition with free biotin. The usefulness of the method was demonstrated by the quantitative recovery of biotinylated proteins from organ homogenates, obtained from mice perfused with a reactive ester derivative of biotin.
机译:链霉亲和素和生物素之间的相互作用是化学和生物学中使用最广泛的工具之一。然而,由于这种复合物的非凡稳定性,从链霉亲和素树脂中释放生物素化蛋白仍然是一个主要问题。我们提出了一种新的协议,用于从链霉亲和素琼脂糖凝胶中定量洗脱生物素化蛋白质,其特点是苛刻的洗脱条件和与游离生物素的竞争。从器官匀浆中定量回收生物素化蛋白可以证明该方法的有效性,匀浆是从灌注有生物素反应性酯衍生物的小鼠体内获得的。

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