Leonov S V, Khristova M L, Sokolova M V, Dönner L, Kharitonenkov I G
Vopr Virusol. 1988 Jan-Feb;33(1):18-21.
A test system has been proposed for the detection of influenza A virus NP protein by solid-phase enzyme immunoassay in a modified system of "double" antibodies: the primary antibodies were F(ab)2-fragments of immunoglobulin class G isolated from rabbit antiserum specific for NP protein which was also used as the source of secondary antibodies. The antigen-bound antibodies were detected by protein A (from St. aureus) conjugate with horseradish peroxidase. The high specificity and sensitivity of the test system (0.3 ng/ml NP protein) and a minimal level of nonspecific reactions were demonstrated. The advantages of this method are discussed.
已经提出了一种检测系统,用于在改良的“双”抗体系统中通过固相酶免疫测定法检测甲型流感病毒核蛋白(NP):一抗是从针对NP蛋白的兔抗血清中分离出的免疫球蛋白G的F(ab)2片段,该抗血清也用作二抗的来源。通过与辣根过氧化物酶结合的蛋白A(来自金黄色葡萄球菌)检测与抗原结合的抗体。该检测系统具有高特异性和灵敏度(0.3 ng/ml NP蛋白),且非特异性反应水平极低。文中讨论了该方法的优点。