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新型化学发光蛋白质免疫印迹封闭及抗体孵育溶液,用于增强抗体 - 抗原相互作用并提高特异性。

Novel chemiluminescent Western blot blocking and antibody incubation solution for enhanced antibody-antigen interaction and increased specificity.

作者信息

Schwartz Kimberly, Bochkariov Dmitry

机构信息

Advansta Inc., Menlo Park, CA, USA.

出版信息

Electrophoresis. 2017 Oct;38(20):2631-2637. doi: 10.1002/elps.201700143. Epub 2017 Aug 25.

DOI:10.1002/elps.201700143
PMID:28704589
Abstract

Western blotting is a ubiquitous tool used in protein and molecular biology research, providing information about the presence, size, relative abundance, and state of a protein in a mixture. First, the proteins in a sample are separated by size using SDS-PAGE then transferred onto a membrane for detection with a set of primary and secondary antibodies. High-quality Western data requires high signal-to-noise ratios, which depend upon reduction of nonspecific antibody interactions. Blocking is a critical step in the Western blot method as it prevents the antibodies from binding nonspecifically to the membrane and irrelevant proteins. A solution of nonfat dry milk (NFDM) in physiological buffer is commonly used for this purpose, but does not perform well with every type of antibody and is not optimal for low-abundance proteins. We present a novel blocking solution for chemiluminescent Western blots, AdvanBlock™-chemi, which outperforms NFDM in experiments with 20 unique antibodies by increasing signal-to-noise ratios and minimizing nonspecific binding. This solution enhances protein detection by Western blot and provides consistent results for detection of low abundant and modified proteins.

摘要

蛋白质免疫印迹法是蛋白质和分子生物学研究中常用的一种工具,可提供有关混合物中蛋白质的存在、大小、相对丰度和状态的信息。首先,使用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)按大小分离样品中的蛋白质,然后转移到膜上,用一组一抗和二抗进行检测。高质量的蛋白质免疫印迹数据需要高信噪比,这取决于减少非特异性抗体相互作用。封闭是蛋白质免疫印迹法中的关键步骤,因为它可防止抗体与膜和无关蛋白质发生非特异性结合。为此,通常使用生理缓冲液中的脱脂奶粉(NFDM)溶液,但它并非对每种类型的抗体都能发挥良好作用,且对于低丰度蛋白质并非最佳选择。我们推出了一种用于化学发光蛋白质免疫印迹的新型封闭液AdvanBlock™-chemi,在针对20种不同抗体的实验中,它通过提高信噪比和最小化非特异性结合,其性能优于NFDM。这种溶液可增强蛋白质免疫印迹法对蛋白质的检测,并为检测低丰度和修饰蛋白质提供一致的结果。

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