Steinberger Birgit, Brem Gottfried, Mayrhofer Corina
Institute of Animal Breeding and Genetics, Department of Biomedical Sciences, University of Veterinary Medicine, A-1210 Vienna, Austria; Institute of Biotechnology in Animal Production, Department of Agrobiotechnology (IFA Tulln), University of Natural Resources and Applied Life Sciences Vienna, A-3430 Tulln, Austria.
Institute of Animal Breeding and Genetics, Department of Biomedical Sciences, University of Veterinary Medicine, A-1210 Vienna, Austria.
Anal Biochem. 2015 May 1;476:17-9. doi: 10.1016/j.ab.2015.01.015. Epub 2015 Jan 30.
Due to post-translational modifications such as phosphorylation, proteins exist as distinct charge variants. Two-dimensional (2D) gel electrophoresis followed by immunoblotting enables the detection of these isoforms. For their accurate relative quantitation in different samples, a loading control is necessary to compensate for technical errors such as imprecise sample loading or transfer. The study reveals that the combinatory approach of SYPRO Ruby and chemiluminescence-based 2D Western blot analysis exhibits high linearity and excellent reproducibility and is applicable for limited sample amounts.
由于磷酸化等翻译后修饰,蛋白质以不同的电荷变体形式存在。二维(2D)凝胶电泳后进行免疫印迹能够检测这些异构体。为了在不同样品中对其进行准确的相对定量,需要一个上样对照来补偿诸如上样不准确或转膜等技术误差。该研究表明,SYPRO Ruby与基于化学发光的二维蛋白质印迹分析相结合的方法具有高线性和出色的重现性,适用于少量样品。