Cruz Walma David A, Collins Joshua W
Cell Biology Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland.
Curr Protoc Cell Biol. 2019 Sep;84(1):e87. doi: 10.1002/cpcb.87.
Whether screening small mammal serum during antibody production or attempting to preserve a stock of precious antibody, this protocol's western blotting method using aliquots containing nanoliter volumes of antibody will benefit researchers. Time-tested western blotting workflows allowing separation and analysis of proteins are routinely utilized in clinical and laboratory settings. The necessity for relatively large quantities of antibody is a major limitation to this universal tool. This article provides a step-by-step protocol for detecting proteins of interest with solutions containing nanoliter volumes of antibody without altering the preceding gel electrophoresis and transfer methods. Important considerations, frequently encountered problems, and means of optimizing reproducibility are discussed. Complementary diagrams, images, and videos are provided. The protocol is demonstrated using 0.3 nanoliters of anti-serum to detect fibronectin in a human foreskin fibroblast cell line. Finally, two support protocols detailing methods of extracting proteins from cultured cells are reported. Published 2019. This article is a US Government work and is in the public domain in the USA.
无论是在抗体生产过程中筛选小型哺乳动物血清,还是试图保存珍贵的抗体储备,本方案中使用含有纳升体积抗体的等分试样的蛋白质印迹法都将使研究人员受益。经过时间考验的蛋白质印迹工作流程可用于分离和分析蛋白质,在临床和实验室环境中经常使用。需要相对大量的抗体是这一通用工具的主要限制。本文提供了一个逐步方案,用于使用含有纳升体积抗体的溶液检测感兴趣的蛋白质,而不改变之前的凝胶电泳和转印方法。讨论了重要注意事项、常见问题以及优化重现性的方法。提供了补充图表、图像和视频。该方案使用0.3纳升抗血清来检测人包皮成纤维细胞系中的纤连蛋白进行了演示。最后,报告了两个详细介绍从培养细胞中提取蛋白质方法的支持方案。2019年发表。本文是美国政府作品,在美国属于公共领域。