Bradley M P, Heslop B F
Hum Genet. 1985;71(2):117-21. doi: 10.1007/BF00283365.
Conditioned culture medium from Daudi cells was used as a source of soluble H-Y antigen. Concentrated culture medium was labeled with 125I and then fractionated by gel filtration. Column fractions were assayed for the presence of H-Y antigen by urease-ELISA. H-Y antigen-containing fractions were then pooled and subjected to an improved immunoprecipitation protocol. Three predominant H-Y antigenic proteins were identified with estimated molecular weights of above 200,000, 50,000, and 20,000.
来自Daudi细胞的条件培养基被用作可溶性H-Y抗原的来源。浓缩培养基用125I标记,然后通过凝胶过滤进行分级分离。通过脲酶-ELISA检测柱分级分离物中H-Y抗原的存在。然后将含有H-Y抗原的分级分离物合并,并进行改进的免疫沉淀方案。鉴定出三种主要的H-Y抗原蛋白,估计分子量分别超过200,000、50,000和20,000。