重组DNA
免疫分析
抗体
抗原
化学
拉布
试剂
噬菌体展示
分子生物学
色谱法
半抗原
生物
免疫学
生物化学
有机化学
基因
GTP酶
作者
Jing Zhao,Peipei Li,A.M. Abd El‐Aty,Lingyuan Xu,Xingmei Lei,Song Gao,Jia Li,Yun Zhao,Yongxin She,Fen Jin,Jing Wang,Bruce D. Hammock,Maojun Jin
标识
DOI:10.1016/j.cej.2024.152039
摘要
Immunoassays have been widely used to determine small-molecule compounds in food and the environment, meeting the challenge of obtaining false positive or negative results because of the variance in the batches of antibodies and antigens. To resolve this problem, atrazine (ATR) was used as a target, and anti-idiotypic nanobodies for ATR (AI-Nbs) and a recombinant full-length antibody against ATR (ATR-rAb) were prepared for the development of a sustainable enzyme-linked immunosorbent assay (ELISA). AI-Nb-7, AI-Nb-58, and AI-Nb-66 were selected from an immune phage display library. ATR-rAb was produced in mammalian HEK293 (F) cells. Among the four detection methods explored, the assay using AI-Nb-66 as a coating antigen and ATR-rAb as a detection reagent yielded a half maximal inhibitory concentration (IC
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