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通过琼脂糖凝胶6B柱层析法纯化小鼠单克隆抗体。

Purification of mouse monoclonal antibodies by chromatography on sepharose 6 B.

作者信息

Diaz-Alonso J M, Kohnert K D, Keilacker H, Ziegler B, Ziegler M

机构信息

Central Institute of Diabetes, Gerhardt Katsch, Karlsburg.

出版信息

Allerg Immunol (Leipz). 1989;35(3):173-9.

PMID:2683682
Abstract

By using Sepharose 6 B, a simple procedure for purification of mouse monoclonal antibodies (mcAbs) of the IgM and IgG class from ascites has been developed. The procedure which was applied to purify mcAbs against insulin and pancreatic islet cells permits either direct chromatographic separation from ascites protein components or after precipitating the immunoglobulins with ammonium sulphate. Recovery of the immunoglobulins was found to be approximately 80%, and the immunological reactivity, as tested by indirect immunofluorescence and ligand binding assay, was almost completely retained. For purification of IgG from ascites, precipitation with ammonium sulphate is recommended prior to chromatography on Sepharose 6 B, whereas IgM can directly be subjected without any pretreatment.

摘要

通过使用琼脂糖凝胶6B,已开发出一种从腹水中纯化IgM和IgG类小鼠单克隆抗体(mcAbs)的简单方法。该方法用于纯化抗胰岛素和胰岛细胞的单克隆抗体,既可以直接从腹水蛋白质成分中进行色谱分离,也可以在用硫酸铵沉淀免疫球蛋白之后进行。发现免疫球蛋白的回收率约为80%,并且通过间接免疫荧光和配体结合试验测试,免疫反应性几乎完全保留。对于从腹水中纯化IgG,建议在琼脂糖凝胶6B上进行色谱分离之前先用硫酸铵沉淀,而IgM无需任何预处理即可直接进行。

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