Larsson A, Wejåker P E, Sjöquist J
Department of Clinical Chemistry, University Hospital, Uppsala, Sweden.
Hybridoma. 1992 Apr;11(2):239-43. doi: 10.1089/hyb.1992.11.239.
A sandwich-ELISA for the detection of protein A from Staphylococcus aureus (SpA) is described, using chicken anti-protein A as a capture antibody and its alkaline phosphatase conjugate for the detection of bound protein A. Traditionally, protein A is detected by its binding to the Fc part of a detector antibody. This binding will be influenced by the presence of other IgG in the protein A solution. However, SpA does not react with the Fc part of chicken IgG, and it is thus possible to detect protein A in IgG containing solutions, such as eluates from protein A-columns. The method can be used to detect 1 x 10(-7) g protein A/l in the presence of serum. The method is more sensitive if no serum or IgG is present in the solution.
本文描述了一种用于检测金黄色葡萄球菌蛋白A(SpA)的夹心酶联免疫吸附测定法(sandwich-ELISA),该方法使用鸡抗蛋白A作为捕获抗体,并使用其碱性磷酸酶缀合物来检测结合的蛋白A。传统上,通过蛋白A与检测抗体的Fc部分结合来检测蛋白A。这种结合会受到蛋白A溶液中其他IgG的存在的影响。然而,SpA不与鸡IgG的Fc部分反应,因此可以在含有IgG的溶液中检测蛋白A,例如蛋白A柱的洗脱液。该方法可用于在血清存在的情况下检测1×10^(-7) g蛋白A/升。如果溶液中不存在血清或IgG,该方法会更灵敏。