免疫PCR为一种高敏感度检测抗原的新技术,操作程序大多沿袭ELISA方法.用戊二醛作连接剂,将蛋白质高效率包被在普通PCR管内壁,使免疫及PCR反应用普通PCR仪得以在管中连贯地进行.实验结果表明,标准曲线的线性关系好,与ELISA方法比较敏感度高出约105.这一改良法的建立,可望促进免疫PCR的普及应用.
The Immuno-PCR antigen detection system has been developed for several years as a modefication of the ELISA method. But only a few of laboratorise applied this high sensitive quantitative assay, since it needs special apparutus or complicated operations.A new procedure of Immuno-PCR was established, which coats antibody or antigien on PCR tubes with 0.8% glutaraldehyde instead of on the wells of titer plates with alkine carbonate buffer. The assay could be coducted with simple handlings and ordinary apparutus, and a high sensitivity is obtained up to 105 times higher than that of ELISA in S-100 antigen detection.
徐平西,肖华胜,鞠躬.一种简易的免疫PCR方法的建立[J].生物化学与生物物理进展,1999,26(4):396-398
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