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一种在十二烷基硫酸钠和其他干扰物质存在的情况下定量蛋白质的固相方法。

A solid-phase method for the quantitation of protein in the presence of sodium dodecyl sulfate and other interfering substances.

作者信息

Sheffield J B, Graff D, Li H P

机构信息

Department of Biology, Temple University, Philadelphia, Pennsylvania 19122.

出版信息

Anal Biochem. 1987 Oct;166(1):49-54. doi: 10.1016/0003-2697(87)90544-6.

Abstract

We describe a simple assay for small amounts of protein that is insensitive to sodium dodecyl sulfate (SDS) or many common interfering substances including Tris and reducing sugars. For this reason, it is particularly useful in the analysis of protein content of samples prior to SDS electrophoresis. The assay consists of the following steps: (i) absorption of protein to nitrocellulose; (ii) fixation of the bound protein with methanol; (iii) staining of the bound protein with amido black; and (iv) elution and spectrophotometric measurement of the bound dye. The assay is sensitive to as little as 0.5 microgram of protein in 1 microliter of solution. Although SDS does not interfere appreciably with measurement, Nonidet-P40 does.

摘要

我们描述了一种用于少量蛋白质的简单检测方法,该方法对十二烷基硫酸钠(SDS)或许多常见的干扰物质(包括Tris和还原糖)不敏感。因此,它在SDS电泳前样品蛋白质含量的分析中特别有用。该检测方法包括以下步骤:(i)蛋白质吸附到硝酸纤维素上;(ii)用甲醇固定结合的蛋白质;(iii)用酰胺黑对结合的蛋白质进行染色;(iv)洗脱并对结合的染料进行分光光度测量。该检测方法对1微升溶液中低至0.5微克的蛋白质敏感。虽然SDS对测量没有明显干扰,但Nonidet-P40有干扰。

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