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无染料蛋白质分子量标准品。

Dye-free protein molecular weight markers.

作者信息

Chang Microsugar, Hsu Hsue-Yin, Lee Han-Jung

机构信息

Institute of Biotechnology and Department of Life Science, National Dong Hwa University, Hualien 97401, Taiwan.

出版信息

Electrophoresis. 2005 Aug;26(16):3062-8. doi: 10.1002/elps.200500041.

Abstract

Protein molecular weight markers are widely used in sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blotting. Here, we describe novel protein molecular weight markers in which a prestaining procedure is no longer needed. Green fluorescent protein (GFP) is stable and resistant to denaturing agents/conditions. Various histidine-tagged GFP fusion proteins were overexpressed in Escherichia coli and purified by metal affinity chromatography. The minimal amount of each protein marker needed for analysis in SDS-PAGE and Western blot under visible light was 62.5 and 125 ng, respectively. Under ultraviolet (UV) ray, the minimal amount of each protein marker needed for analysis in SDS-PAGE and Western blot was half of those amounts used under visible light, respectively. Collectively, the accuracy, sensitivity, ease, economy, and flexibility of our strategy may reinforce the application of GFP in molecular biology.

摘要

蛋白质分子量标准物在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和蛋白质免疫印迹法中被广泛应用。在此,我们描述了一种新型蛋白质分子量标准物,其不再需要预染程序。绿色荧光蛋白(GFP)稳定且耐变性剂/变性条件。各种组氨酸标签的GFP融合蛋白在大肠杆菌中过量表达,并通过金属亲和层析进行纯化。在可见光下,SDS-PAGE和蛋白质免疫印迹分析所需的每种蛋白质标准物的最小量分别为62.5 ng和125 ng。在紫外线(UV)下,SDS-PAGE和蛋白质免疫印迹分析所需的每种蛋白质标准物的最小量分别是可见光下使用量的一半。总体而言,我们方法的准确性、灵敏度、简便性、经济性和灵活性可能会加强GFP在分子生物学中的应用。

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