Lindqvist L
Vox Sang. 1982 Mar;42(3):124-30. doi: 10.1111/j.1423-0410.1982.tb01081.x.
A rocket affinoelectrophoretic assay system was used to detect and quantify the human salivary ABH-blood group antigens of 155 individuals. In this system blood group antigens precipitated as rockets in agarose gels containing different lectins, with the rocket height being correlated to the antigen concentration. This technique was compared with the classical hemagglutination inhibition method for determination of salivary blood group antigens, and it was demonstrated that salivary A, B and H blood group antigens were detected with the lectins from helix pomatia, Bandeiraea simplicifolia and Ulex europeus, respectively. The technique was rapid and sensitive, with a detection limit of 0.1 microliters saliva. This technique can also be used for determination of blood group antigens derived from other body fluids, tissues and cells.
采用火箭免疫电泳分析系统对155名个体的人唾液ABH血型抗原进行检测和定量。在该系统中,血型抗原在含有不同凝集素的琼脂糖凝胶中呈火箭状沉淀,火箭高度与抗原浓度相关。将该技术与测定唾液血型抗原的经典血凝抑制法进行比较,结果表明,分别用圆口螺、单叶相思豆和欧洲荆豆的凝集素检测到唾液中的A、B和H血型抗原。该技术快速、灵敏,唾液检测限为0.1微升。该技术还可用于测定来自其他体液、组织和细胞的血型抗原。