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一种蛋白质估测方法,该方法对于简单蛋白质能产生近乎恒定的颜色反应,并消除四种已知干扰剂的影响:肽基团的微量测定。

A protocol for protein estimation that gives a nearly constant color yield with simple proteins and nullifies the effects of four known interfering agents: microestimation of peptide groups.

作者信息

Raghupathi R N, Diwan A M

机构信息

Department of Zoology, University of Poona, India.

出版信息

Anal Biochem. 1994 Jun;219(2):356-9. doi: 10.1006/abio.1994.1276.

Abstract

A modified version of the Lowry protocol for protein measurement is being introduced in which the increment in color due to copper-protein interactions can be directly equated to the concentration of peptide groups (the CO-NH moieties) present in the sample. The method provides an accurate estimation of protein concentrations in the range of 5-40 micrograms, with a sensitivity similar to that of the original assay procedure. It yields hardly any protein-to-protein variation with simple proteins and eliminates the interference by four compounds that commonly affect the Lowry assay. A numerical factor has been calculated that allows conversion of micromoles of peptide groups into actual micrograms of protein present in the sample.

摘要

一种用于蛋白质测量的改良版洛瑞法正在被引入,其中由于铜 - 蛋白质相互作用导致的颜色增量可直接等同于样品中存在的肽基团(-CO-NH部分)的浓度。该方法能准确估计5 - 40微克范围内的蛋白质浓度,灵敏度与原始测定方法相似。对于简单蛋白质,它几乎不会产生蛋白质间的差异,并且消除了通常影响洛瑞法的四种化合物的干扰。已经计算出一个数值因子,可将肽基团的微摩尔数转换为样品中实际存在的蛋白质微克数。

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