快速蛋白质液相色谱法
色谱法
化学
大小排阻色谱法
离子色谱法
离子交换
高效液相色谱法
寡核苷酸
离子
生物化学
DNA
有机化学
酶
作者
Ashkan Madadlou,Siobhan O’Sullivan,David Sheehan
标识
DOI:10.1007/978-1-60761-913-0_25
摘要
Fast protein liquid chromatography (FPLC) is a form of high-performance chromatography that takes advantage of high resolution made possible by small-diameter stationary phases. It was originally developed for proteins and features high loading capacity, biocompatible aqueous buffer systems, fast flow rates, and availability of stationary phases in most common chromatography modes (e.g., ion exchange, gel filtration, reversed phase, and affinity). The system makes reproducible separation possible by incorporating a high level of automation including autosamplers, gradient program control, and peak collection. In addition to proteins, the method is applicable to other kinds of biological samples including oligonucleotides and plasmids. The most common type of FPLC experiment is anion exchange of proteins. This chapter describes such an experiment carried out using an ÄKTA FPLC explorer system (Amersham Pharmacia Biotech, Sweden).
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