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H4亚型禽流感血凝素单克隆抗体的制备及夹心ELISA法的建立

[Preparation of monoclonal antibody against hemagglutinin of H4 subtype avian influenza and establishment of sandwich ELISA].

作者信息

Deng Xianwen, Luo Sisi, Xie Zhixun, Huang Jiaoling, Zhang Minxiu, Xie Zhiqin, Xie Liji, Fan Qing, Wang Sheng, Zeng Tingting, Zhang Yanfang

机构信息

Guangxi Veterinary Research Institute, Guangxi Key Laboratory of Veterinary Biotechnology, Nanning 530001, China.

Guangxi Veterinary Research Institute, Guangxi Key Laboratory of Veterinary Biotechnology, Nanning 530001, China. *Corresponding author, E-mail:

出版信息

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2020 Jan;36(1):69-74.

Abstract

Objective To prepare the monoclonal antibodies (mAb) against hemagglutinin of H4 subtype avian influenza virus (AIV), and develop a sandwich ELISA for the detection of H4 subtype AIV. Methods The BALB/c mice were immunized with inactive H4 subtype AIV. A mAb against H4 subtype AIV, designated as 6G4, was obtained by cell fusion, hemagglutination inhibition (HI) screening and subcloing. Immuofluorescence cytochemistry and Western blotting were used to detect the reactivity of 6G4 with H4 subtype AIV, and the specificity, broad spectrum and stability of 6G4 were characterized by HI assay. Subclass of 6G4 was determined by kit. With chicken polyclonal antibody against H4 subtype AIV as coated antibody, 6G4 mAb as capture antibody and HRP-labeled goat anti-mouse IgG as the enzyme-labeled antibody, a sandwich ELISA for the detection of H4 subtype AIV was established by optimization of the reaction conditions and serial verification. Results 6G4 belonged to IgG1 subclass, and the light chain belonged to κ. It could secrete antibody stably and had good reactivity, specificity, broad spectrum and stability. ELISA based on 6G4 was specific, sensitive, accurate and suitable for the detection of a large number of samples. Conclusion We successfully achieved the anti-H4 subtype AIV mAb, and developed the sandwich ELISA for the detection of H4 subtype AIV.

摘要

目的 制备抗H4亚型禽流感病毒(AIV)血凝素的单克隆抗体(mAb),并建立用于检测H4亚型AIV的夹心酶联免疫吸附测定(ELISA)。方法 用灭活的H4亚型AIV免疫BALB/c小鼠。通过细胞融合、血凝抑制(HI)筛选和亚克隆获得一株抗H4亚型AIV的单克隆抗体,命名为6G4。采用免疫荧光细胞化学和蛋白质印迹法检测6G4与H4亚型AIV的反应性,通过HI试验对6G4的特异性、广谱性和稳定性进行鉴定。用试剂盒测定6G4的亚类。以鸡抗H4亚型AIV多克隆抗体为包被抗体,6G4单克隆抗体为捕获抗体,辣根过氧化物酶(HRP)标记的山羊抗小鼠IgG为酶标抗体,通过优化反应条件和系列验证,建立了检测H4亚型AIV的夹心ELISA。结果 6G4属于IgG1亚类,轻链属于κ链。其能稳定分泌抗体,具有良好的反应性、特异性、广谱性和稳定性。基于6G4的ELISA具有特异性强、灵敏度高、准确性好等特点,适用于大量样品的检测。结论 成功获得了抗H4亚型AIV单克隆抗体,并建立了检测H4亚型AIV的夹心ELISA。

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