抗血清
琼脂糖
抗体
色谱法
化学
免疫分析
蛋白质纯化
抗原
蛋白质A
亲和层析
产量(工程)
分子生物学
生物化学
生物
免疫学
材料科学
酶
冶金
作者
Robert Hnasko,Jeffery A. McGarvey
标识
DOI:10.1007/978-1-4939-2742-5_3
摘要
Antibodies are provided in a variety of formats that include antiserum, hybridoma culture supernatant, or ascites. They can all be used successfully in crude form for the detection of target antigens by immunoassay. However, it is advantageous to use purified antibody in defined quantity to facilitate assay reproducibility, economy, and reduced interference of nonspecific components as well as improved storage, stability, and bio-conjugation. Although not always necessary, the relative simplicity of antibody purification using commercially available protein-A, protein-G, or protein-L resins with basic chromatographic principles warrants purification when antibody source material is available in sufficient quantity. Here, we define three simple methods using immobilized (1) protein-A, (2) protein-G, and (3) protein-L agarose beads to yield highly purified antibody.
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