Gerdes M, Meusel M, Spener F
Institut für Chemo- und Biosensorik, Münster, Germany.
Anal Biochem. 1997 Oct 1;252(1):198-204. doi: 10.1006/abio.1997.2301.
An enzyme-linked immunosorbent assay-based displacement assay was developed for the determination of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). Advantage was taken of the cross-reactivity of a monoclonal anti-2,4-D antibody toward 2-methyl-4-chlorophenoxyacetic acid (MCPA). MCPA was conjugated with bovine serum albumin (BSA), immobilized on the surface of a microtiter plate, and saturated with the anti-2,4-D antibody. Due to the low affinity of the antibody toward MCPA (cross-reactivity of approximately 30%), the addition of 2,4-D resulted in a displacement of the antibody. Remaining antibodies were subsequently detected using a peroxidase-labeled goat anti-mouse antibody. The detection limit was as low as 0.1 microgram/liter for 2,4-D, which complies with the European Union Drinking Water Directives. When 2,4-D-BSA was used instead of MCPA-BSA conjugates, no significant displacement of bound antibody was observed.
开发了一种基于酶联免疫吸附测定的置换分析法,用于测定除草剂2,4-二氯苯氧乙酸(2,4-D)。利用单克隆抗2,4-D抗体对2-甲基-4-氯苯氧乙酸(MCPA)的交叉反应性。将MCPA与牛血清白蛋白(BSA)偶联,固定在微量滴定板表面,并用抗2,4-D抗体饱和。由于抗体对MCPA的亲和力较低(交叉反应性约为30%),加入2,4-D会导致抗体被置换。随后使用过氧化物酶标记的山羊抗小鼠抗体检测剩余的抗体。2,4-D的检测限低至0.1微克/升,符合欧盟饮用水指令。当使用2,4-D-BSA代替MCPA-BSA偶联物时,未观察到结合抗体的明显置换。