Bannikova E M, Nasonov E L, Tishchenko V A, Nagornaia L V, Sura V V
Biull Eksp Biol Med. 1989 Jul;108(7):99-101.
An ELISA procedure was developed for measuring serum amyloid P-component (SAP). The assay is based on our finding of binding AP to polystyrene microtiter plates. The amount of SAP is determined by concurrent ELISA, wells being sequentially incubated with rabbit anti-AP antiserum and goat anti-rabbit antiserum, conjugated with peroxidase. The limit of sensitivity of the assay is 0.5 micrograms/ml. When applied to the screening of patients plasma, elevation of SAP concentration in patients with rheumatoid arthritis and amyloidosis were found.
开发了一种用于测量血清淀粉样蛋白P成分(SAP)的酶联免疫吸附测定(ELISA)程序。该检测基于我们发现的AP与聚苯乙烯微量滴定板的结合。通过同步ELISA测定SAP的量,孔依次与兔抗AP抗血清和与过氧化物酶偶联的山羊抗兔抗血清孵育。该检测的灵敏度极限为0.5微克/毫升。当应用于患者血浆筛查时,发现类风湿性关节炎和淀粉样变性患者的SAP浓度升高。