Aoki Y, Funayama M, Sagisaka K
Department of Forensic Medicine, Tohoku University School of Medicine, Sendai.
Tohoku J Exp Med. 1987 Jul;152(3):277-81. doi: 10.1620/tjem.152.277.
A new method for detection of AB antigen from blood stain using enzyme-linked immunosorbent assay (ELISA) is described. Flat-bottomed-wells of polystylen plate coated with human anti-B or rabbit anti-A were sensitized with AB antigen which was extracted from blood stain with 1% octyl-glucopyranoside in 0.1 M phosphate buffer pH 8.0. Mouse monoclonal anti-A or anti-B, and peroxidase conjugated anti-mouse immunoglobulin were added to the wells, respectively. Subsequently, the substrate was dropped into the wells, and the absorbance of the solution was measured. By this method, we could distinguish AB group blood stain from the mixed stain of A and B group bloods. When rabbit antiserum was used as the first antibody, differentiation between these antigens was unsuccessful presumably because of non-specific adsorption.
本文描述了一种使用酶联免疫吸附测定法(ELISA)从血迹中检测AB抗原的新方法。用1%辛基吡喃葡萄糖苷在pH 8.0的0.1M磷酸盐缓冲液中从血迹中提取的AB抗原致敏包被有抗人B或抗兔A的聚苯乙烯板平底孔。分别向孔中加入小鼠单克隆抗A或抗B以及过氧化物酶偶联的抗小鼠免疫球蛋白。随后,将底物滴入孔中,并测量溶液的吸光度。通过这种方法,我们可以将AB型血迹与A、B型血迹的混合污渍区分开来。当使用兔抗血清作为一抗时,由于非特异性吸附,这些抗原之间的区分未成功。