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机构地区:[1]第二军医大学医学生物技术和分子遗传研究所免疫室
出 处:《中华微生物学和免疫学杂志》1994年第5期353-355,共3页Chinese Journal of Microbiology and Immunology
摘 要:对酶标记链球菌蛋白G(SPG)在ELISA的应用条件进行了研究并与SPA作了系统比较。SPG与IgG结合受温度影响,37℃结合活性高于室温和4℃;反应时间定为2h反应溶液pH值升高,SPG的结合力亦增强。在同等条件下与酶标记SPA进行比较,结果表明SPG对小鼠单克隆抗体、羊抗人、兔抗IFN-γ和驴抗兔Igg以及牛、大鼠和人IgG的结合力均明显高于SPA。SPG用于大鼠血清抗IFN-γ抗体的检测,其阳性率和抗体滴度均大大高于SPA。因此,SPG作为一种广谱的、高亲和力的IgG结合物,是应用于ELISA的理想的替代二抗。treptococcal protein G(SPG)as a novel IgG-binding reagent was first applied in ELISA and the optimal con-ditions of temperature,incubation time and the pH value of buffer for the int eraction of SPG and lgG in ELISAwere established.The affinity of enzyme conjugated SPG and SPA to IgGs were compared under the same condi-tions. The results revealed the affinity of SPG to monoclonal IgG and polyclonal IgGs of goat,rabbit,donkey,cow, rat and human were much hlgher than that of SPA.T he positive ratio and the titers of antibody were alsoBteatly elevatedwhen SPG was used in detecting the antibody in rat sera. Therefore,SPG may be an ideal alterna-tive antibody in ELISA as a IgG conjugate with wide spectrum and high affinity.
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