Mottolese M, Iacona A, Natali P G
Immunol Commun. 1980;9(4):379-87. doi: 10.3109/08820138009052984.
Bovine serum albumin labeled with alkaline phosphatase and antibody have been employed as a model to determine if the use of Protein A bearing Staphylococcus aureus Cowan I strain (SACI) bacteria could be extended to enzyme immunoassay (EIA). SACI do not activate "per se" the enzyme substrate and bind aspectifically minimum amount of enzyme labeled antigen. Experimental conditions are described for the use of SACI both in macro and micro EIA assay which allows the processing of numerous samples with minimum handling. The sensitivity of the EIA is comparable with radioassy (EIA 2ng-RIA 4ng) which uses SACI in place of second antibody. The inhibition test can be performed in 4 hours time. These results suggest that the stability of SACI when combined with that of enzyme labeled antigens can widen the use of EIA, both for investigative and clinical studies.
以碱性磷酸酶标记的牛血清白蛋白和抗体作为模型,来确定携带金黄色葡萄球菌考恩I株(SACI)的蛋白A是否可用于酶免疫测定(EIA)。SACI本身不会激活酶底物,且非特异性结合的酶标记抗原量极少。文中描述了在宏观和微观EIA测定中使用SACI的实验条件,该条件允许以最少的操作处理大量样本。EIA的灵敏度与使用SACI代替第二抗体的放射免疫测定法相当(EIA为2ng,RIA为4ng)。抑制试验可在4小时内完成。这些结果表明,SACI与酶标记抗原结合时的稳定性能够扩大EIA在研究和临床研究中的应用。