Putalun Waraporn, Fukuda Noriko, Tanaka Hiroyuki, Shoyama Yukihiro
Faculty of Pharmaceutical Sciences, Khon Kaen University, 40002, Khon Kaen, Thailand.
Anal Bioanal Chem. 2004 Mar;378(5):1338-41. doi: 10.1007/s00216-003-2408-x. Epub 2004 Jan 28.
An immunochromatographic strip test has been developed for detecting ginsenosides Rb1 (G-Rb1) and Rg1 (G-Rg1). This qualitative assay system is useful as a rapid screening method for detecting G-Rb1 and G-Rg1 in plants and plant preparations. Our assay is a competitive immunoassay that uses anti-G-Rb1 and anti-G-Rg1 monoclonal antibodies (MAbs) and a detection reagent that contains colloidal gold particles coated with anti-G-Rb1 and anti-G-Rg1 MAbs. Detection limits are 2 microg mL(-1) for both G-Rb1 and G-Rg1.
已开发出一种免疫层析试纸条检测方法,用于检测人参皂苷Rb1(G-Rb1)和Rg1(G-Rg1)。这种定性检测系统作为一种快速筛选方法,可用于检测植物及植物制品中的G-Rb1和G-Rg1。我们的检测方法是一种竞争性免疫分析,使用抗G-Rb1和抗G-Rg1单克隆抗体(MAbs)以及一种检测试剂,该试剂含有包被有抗G-Rb1和抗G-Rg1单克隆抗体的胶体金颗粒。G-Rb1和G-Rg1的检测限均为2微克/毫升。