多克隆抗体
抗体
免疫沉淀
表位
免疫印迹
分子生物学
免疫细胞化学
靶蛋白
核酸
生物
蛋白质纯化
生物化学
化学
基因
免疫学
内分泌学
作者
Swathi Arur,Tim Schedl
出处
期刊:Nature Protocols
[Nature Portfolio]
日期:2014-01-23
卷期号:9 (2): 375-395
被引量:22
标识
DOI:10.1038/nprot.2014.017
摘要
Post-translational modifications alter protein structure, affecting activity, stability, localization and/or binding partners. Antibodies that specifically recognize post-translationally modified proteins have a number of uses including immunocytochemistry and immunoprecipitation of the modified protein to purify protein-protein and protein-nucleic acid complexes. However, antibodies directed at modified sites on individual proteins are often nonspecific. Here we describe a protocol to purify polyclonal antibodies that specifically detect the modified protein of interest. The approach uses iterative rounds of subtraction and affinity purification, using stringent washes to remove antibodies that recognize the unmodified protein and low sequence complexity epitopes containing the modified amino acid. Dot blot and western blot assays are used to assess antibody preparation specificity. The approach is designed to overcome the common occurrence that a single round of subtraction and affinity purification is not sufficient to obtain a modified protein-specific antibody preparation. One full round of antibody purification and specificity testing takes 6 d of discontinuous time.
科研通智能强力驱动
Strongly Powered by AbleSci AI