Preparation and identification of anti human myocardium troponin I monoclonal antibodies
- VernacularTitle:人心肌肌钙蛋白I单克隆抗体的制备及鉴定
- Author:
Bao-Ming JIAO
1
;
Zhi-Liang LI
;
Qing LU
;
Hong-Jin QIAN
;
Ning ZHOU
;
Su-Hua WANG
;
Xue-Xian QIAN
Author Information
1. PLA Guangzhou Military Area Command
- From:
Academic Journal of Second Military Medical University
2001;22(4):376-377
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To prepare monoclonal antibodies (McAb) with cardiac troponin I (cTnI) which was purified from fresh human cardiac muscle within 6 h. Methods: (1) Extraction and purification of human cTnI: cTnI was purified by high salt extraction, saltless precipitation, 65℃ treatment, ammonium sulfate fractionation and DEAE-cellulose chromatography, etc. (2) Preparation of anti human cTnI McAb: The purified cTnI was injected into the spleen of BALB/c mice. The cTnI-primed spleen cells were fused with Sp2/0 myoloma cell. The McAbs anti human cTnI were obtained by screening with indirect ELISA and 3 times clone. (3)The identification of anti cTnI McAb. Results: Five hybridoma cell lines, named 3A7，3A11，3D2，3F10 and 1H9 were developed, which could secret McAb stably. The 5 McAbs all were demonstrated to be IgG2a by double gel diffusion test. The number of hybridoma chromosomes was between 92 to 110 and the chromosomes were mainly telocentric. Five kinds of ascites had no cross-reaction to LDH，CK，CK-MB ，AST and cardiac troponin T(cTnT), and their titers were between 3.2×10-6 to 1.6×10-7. Conclusion: 3D2，3F10 and 3A7,3A11,1H9 react to different epitopes of cTnI.
