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Preparation and Identification of Monoclonal Antibody Against Equine Chorionic Gonadotropin

SU Xiao-qian1, DENG Liang1, JIA Yu2, HAN Guo-cai1,3   

  1. 1. College of Animal Science and Technolgy, China Agricultural Univeristy, Beijing 100193, China;
    2. Beijing Qinbang Biological Technology Co., Ltd.,Beijing 100026, China;
    3. Equine Research Center, China Agricultural Univeristy, Beijing 100193, China
  • Received:2012-02-27 Online:2012-09-20 Published:2012-09-18

Abstract: This study fusing the spleen cells of BALB/c mice which was immunized with high purified equine chorionic gonadotropin and myeloma cells SP2/0 at the rate of 1∶10, and screening the positive cloning by the means of indirect enzyme linked immunosorbent assay. Positive cells were clone through limited dilution method, injecting the mixture into the abdominal cavity of mice after intermediate cultured. Antibody titer was assayed by ways of indirect ELISA. Eight hybridoma cell lines were obtained which could secrete eCG stably, titer reached above 10-5. The obtained eCG hybridoma cell lines, which laid a foundation to assay the level of eCG.

Key words: equine chorionic gonadotropin; hybridoma cell line; monoclonal antibody; enzyme linked immunesorbent assay

CLC Number: