›› 2017, Vol. 44 ›› Issue (10): 3049-3056.doi: 10.16431/j.cnki.1671-7236.2017.10.031

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Preparation of Monoclonal Antibody Against Lasalocid and Deveopment of Indirect Competitive ELISA Detection Method

YANG Xiao-kang1,2, ZHANG Hui-yan1,2, GU Jian-hong1,2, YUAN Yan1,2, BIAN Jian-chun1,2, LIU Zong-ping1,2, LIU Xue-zhong1,2   

  1. 1. College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China;
    2. Jiangsu Coinnovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, China
  • Received:2017-04-18 Online:2017-10-20 Published:2017-10-20

Abstract:

To prepare monoclonal antibodies (MAb) against lasalocid (LAS) and establish an indirect competitive ELISA (Ci-ELISA) detection method,conjuaction of LAS-BSA and LAS-OVA were synthetized as the immunogen and coating antigen by using active ester method in this experiment. After 6 times of immunization,the spleen cells of mice and myeloma cells were fused. Finally,a hybridoma cell line that could stably secrete specific MAb against LAS was screened.The immunological subtype of the MAb was identified as IgG1,and its light chain was κ type.The titer of the ascites was 1:16 000, which showed no cross activity with monensin sodium, salinomycin sodium,maduramycin,cefalotin sodium and streptomycin sulfate. Ci-ELISA method was established based on the MAb against LAS with the linear equation was y=0.376x-0.2374(R2=0.9914), and the linear range was 5 to 1 000 ng/mL and the IC50 was 90.22 ng/mL. The method was used to detect LAS in spiked samples and the recovery rate was 81.76% to 102.41% within the detection range,indicating that the method was successfully established with good accuracy and high sensitivity. The preparation of MAb against LAS and the establishment of Ci-ELISA method laid the foundation for the development of LAS detection kit.

Key words: lasalocid; hapten; monoclonal antibody; indirect competitive ELISA

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