Brunner M, Wachtel S, Kent M, Drost M, Goff A, Betteridge K
Center for Reproductive Biology, Collierville, TN 38017.
Differentiation. 1987;35(2):122-5. doi: 10.1111/j.1432-0436.1987.tb00159.x.
A newly developed enzyme-linked immunosorbent assay (ELISA) was applied for studying H-Y antigen in buffaloes, cattle, horses and humans. A monoclonal H-Y antibody was absorbed with cells from males or females and was then tested against fluid samples known to contain soluble H-Y antigen. In this system, positive absorption manifested itself by a fall in optical density relative to the optical density scored using unabsorbed antibody; this finding signified the presence of H-Y in the absorbing cells. In each of the four species, the fall in optical density was pronounced after absorption with male cells, but some decrease was also evident after absorption with female cells, indicating a degree of nonspecific attachment of the antibody.
一种新开发的酶联免疫吸附测定法(ELISA)被用于研究水牛、牛、马和人类中的H-Y抗原。一种单克隆H-Y抗体用来自雄性或雌性的细胞进行吸附,然后针对已知含有可溶性H-Y抗原的液体样本进行检测。在这个系统中,阳性吸附表现为相对于使用未吸附抗体所记录的光密度,光密度下降;这一发现表明吸附细胞中存在H-Y。在这四个物种中的每一个中,用雄性细胞吸附后光密度明显下降,但用雌性细胞吸附后也有一些下降,这表明抗体存在一定程度的非特异性附着。