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45千道尔顿雌莫司汀结合蛋白(EMBP)的纯化及其抗体的制备。

Purification of 45 KDa estramustine binding protein (EMBP) and preparation of its antibody.

作者信息

Yuasa H, Yamanaka H, Imai K, Mashimo T, Kohno H

机构信息

Department of Urology, Gunma University School of Medicine.

出版信息

Hinyokika Kiyo. 1990 Feb;36(2):121-5.

PMID:2343804
Abstract

The purification of 45 KDa EMBP and the production of monospecific anti-serum is described. 45 KDa EMBP was purified by relatively simple methods using ion exchange HPLC (TSK-GEL DEAE-5PW column) and size exclusion HPLC (TSK-GEL G3000SW column). The results clearly demonstrated the speed and simplicity of the method using these columns, compared to previously-described methods for purification of 45 KDa EMBP.

摘要

本文描述了45 kDa EMBP的纯化及单特异性抗血清的制备。采用离子交换高效液相色谱法(TSK-GEL DEAE-5PW柱)和尺寸排阻高效液相色谱法(TSK-GEL G3000SW柱),通过相对简单的方法对45 kDa EMBP进行了纯化。结果清楚地表明,与先前描述的45 kDa EMBP纯化方法相比,使用这些色谱柱的方法具有速度快和操作简单的特点。

相似文献

1
Purification of 45 KDa estramustine binding protein (EMBP) and preparation of its antibody.45千道尔顿雌莫司汀结合蛋白(EMBP)的纯化及其抗体的制备。
Hinyokika Kiyo. 1990 Feb;36(2):121-5.
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引用本文的文献

1
Production of monoclonal antibody against the C1 component of rat estramustine-binding protein: immunohistochemical study of rat prostate.抗大鼠雌莫司汀结合蛋白C1成分单克隆抗体的制备:大鼠前列腺的免疫组织化学研究
Histochem Cell Biol. 1995 Dec;104(6):429-33. doi: 10.1007/BF01464332.