Ogata M, Nakasono I, Iwasaki M, Kubo S, Fukae T, Suyama H, Narita K
Department of Legal Medicine, Nagasaki University School of Medicine, Japan.
J Forensic Sci. 1987 Nov;32(6):1551-7.
It is known that rabbit anti-gum arabic (GA) serum has cross-reactivity with Lea antigen, and that, by using this cross-reactive anti-Lea antibody, the presence of Lea antigen in red blood cells and saliva can be demonstrated with accuracy. We have devised a rapid and highly sensitive method for detecting Lea substance in human saliva by the enzyme-linked immunosorbent assay (ELISA) method using an anti-Lea antibody isolated from anti-GA serum by affinity chromatography on Synsorb Lea. The ELISA plate, coated with the specific anti-Lea antibody, adsorbed the Lea substance in saliva which was subsequently identified by adding enzyme labeled anti-Lea IgG in that order. The method could detect the Lea substance in Le(a+) saliva stains as small as 0.1 by 0.1 cm in size that had been stored at room temperature for three weeks and in Le(a+) saliva stains 0.7 by 0.7 cm in size that had been stored for ten years. This method seems to be useful for quantitative analyses of the Lea substance in various body fluids.
已知兔抗阿拉伯树胶(GA)血清与Lea抗原具有交叉反应性,并且通过使用这种交叉反应性抗Lea抗体,可以准确地证明红细胞和唾液中Lea抗原的存在。我们设计了一种快速且高度灵敏的方法,通过酶联免疫吸附测定(ELISA)法,使用通过在Synsorb Lea上进行亲和层析从抗GA血清中分离出的抗Lea抗体来检测人唾液中的Lea物质。涂有特异性抗Lea抗体的ELISA板吸附唾液中的Lea物质,随后通过依次添加酶标记的抗Lea IgG来进行鉴定。该方法能够检测出大小为0.1×0.1厘米、在室温下保存三周的Le(a+)唾液斑中的Lea物质,以及大小为0.7×0.7厘米、保存了十年的Le(a+)唾液斑中的Lea物质。这种方法似乎对各种体液中Lea物质的定量分析很有用。