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采用酶联免疫吸附测定法(ELISA)以及用酶标记的抗G3m(21)单克隆抗体进行斑点免疫结合法进行G3m(21)分型。

G3m(21) typing by ELISA and dot immunobinding with enzyme-labeled monoclonal anti-G3m(21) antibody.

作者信息

Kishida T, Tamaki Y, Fukuda M

机构信息

Department of Forensic Medicine, Medical College of Oita, Japan.

出版信息

Z Rechtsmed. 1988;101(1):15-20. doi: 10.1007/BF00205319.

Abstract

Simple, rapid methods are described for G3m(21) typing with peroxidase-labeled monoclonal anti-G3m(21) antibody. In G3m(21) typing by ELISA, microtiter wells were coated directly with the test antigen, which was detected with the enzyme-labeled monoclonal antibody. To further simplify the procedure, a dot immunobinding method was developed. The antigen in the test serum applied onto a nitrocellulose membrane was successfully detected with the enzyme-labeled monoclonal antibody. These methods, particularly the dot immunobinding, are suitable for forensic casework because they are rapid and simple and require no technical skill.

摘要

本文描述了用辣根过氧化物酶标记的抗G3m(21)单克隆抗体进行G3m(21)分型的简单、快速方法。在ELISA法进行G3m(21)分型时,微量滴定板孔直接包被检测抗原,并用酶标单克隆抗体进行检测。为进一步简化操作程序,开发了斑点免疫结合法。应用于硝酸纤维素膜上的检测血清中的抗原,用酶标单克隆抗体成功检测到。这些方法,尤其是斑点免疫结合法,适用于法医检验工作,因为它们快速、简单,且无需技术技巧。

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