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Development of a polyclonal antibody based icELISA for detection of testosterone levels in sheep

机译:基于多克隆抗体的icelisa检测绵羊睾酮水平的多克隆抗体

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An indirect competitive ELISA (icELISA) has been developed for the determination of testosterone (TES) residue in urine. For this reason, EDC method was employed to synthesize the artificial antigen of TES-BSA, and New Zealand white rabbits were used to prepare the polyclonal antibody. Based on the square matrix titration, an icELISA method was developed. The dynamic range was from 0.096 to 92.2 ng/mL, with LOD and IC50 value of 0.035 ng/mL and 2.8 ng/mL, respectively. Except for a slight cross-reactivity (22.3%) to 19-nortestosterone, negligible cross-reactivity to other compounds was observed. After optimization, 20-fold dilution in sheep urine gave an inhibition curve almost the same as that in PBS buffer. The regression equation was y = 0.9186 × + 1.4569, with a correlation coefficient of 0.9852. Therefore, this assay has the potential to be incorporated into a quantitative monitoring program for the rapid screening of TES residue in urine.
机译:开发了间接竞争力的ELISA(ICELISA)用于测定尿液中的睾酮(TES)残留物。因此,采用EDC方法合成TES-BSA的人工抗原,新西兰白兔用于制备多克隆抗体。基于方矩阵滴定,开发了一种icelisa方法。动态范围为0.096至92.2ng / ml,含有0.035ng / ml和2.8ng / ml的LOD和IC 50 值。除了轻微的交叉反应性(22.3%)至19-nortosterone,观察到与其他化合物的可忽略不计的交叉反应性。优化后,绵羊尿液中的20倍稀释几乎与PBS缓冲液中的抑制曲线相同。回归方程为y = 0.9186×+ 1.4569,相关系数为0.9852。因此,该测定具有潜力掺入尿液中快速筛选TES残留的定量监测计划中。

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