用A-Sepharose蛋白从小鼠血清中分离纯化IgG1、IgG2a和IgG2b免疫球蛋白

P.L. Ey, S.J. Prowse, C.R. Jenkin
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引用次数: 2533

摘要

本文描述了一种简单、快速的分离小鼠IgG1、IgG2a和IgG2b免疫球蛋白的方法,其产率接近100%。用蛋白a - sepharose 4B对小鼠血清进行分离,测定免疫球蛋白的回收率随pH值的变化。当pH值为8.0时,将血清置于柱上,排出液中IgM、IgA和IgE与非免疫球蛋白血清成分几乎可以定量回收。如果不超过柱的结合能力,基本上所有的IgG都保留在pH 8.0下,并且不能通过洗涤洗脱。使用降低pH的缓冲液,IgG1, IgG2a和IgG2b分别在pH 6.0-7.0, pH 4.5-5.0和pH 3.5-4.0下依次洗脱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation of pure IgG1, IgG2a and IgG2b immunoglobulins from mouse serum using protein A-Sepharose

A simple and rapid method for isolating pure mouse IgG1, IgG2a and IgG2b immunoglobulins in nearly 100% yield is described. Mouse serum was fractionated on protein A-Sepharose 4B and the recovery of immunoglobulins was measured as a function of pH. When serum was applied to the column at pH 8.0, IgM, IgA and IgE were almost quantitatively recovered in the effluent together with non-immunoglobulin serum components. Providing the binding capacity of the column was not exceeded, essentially all IgG was retained at pH 8.0 and this could not be eluted by washing. Using buffers of decreasing pH, IgG1, IgG2a and IgG2b were sequentially eluted at pH 6.0–7.0, pH 4.5–5.0 and pH 3.5–4.0, respectively.

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