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Method of diagnosing cystic fibrosis patients and asymptomatic carrier of the cystic fibrosis gene

机译:诊断囊性纤维化患者的方法和囊性纤维化基因的无症状载体

摘要

An immunologic method has been devised enabling diagnosis of patients with cystic fibrosis, as well as asymptomatic carriers of the cystic fibrosis gene. Mono-specific antibody to Cystic Fibrosis Protein (CFP) is inserted into a first position on an electrophoresis plate. A body fluid from the subject to be tested is placed into a second position on the plate. An electrical potential is imposed across the positions with the anode being adjacent to the section containing the serum and the cathode being adjacent to the section containing the antibody. The presence of Cystic Fibrosis Protein is indicated by one or more precipitation zones forming where the body fluid proteins meet the antibody due to movement induced by an applied electrical potential. The relative position of the precipitation zone between the first and second positions, or the area of the precipitation zone, indicates a concentration of the Cystic Fibrosis Protein. Methods for producing the purified Cystic Fibrosis Protein antibody and for purifying the Cystic Fibrosis Protein itself are also disclosed.
机译:已经设计出一种免疫学方法,能够诊断患有囊性纤维化以及囊性纤维化基因的无症状携带者。囊性纤维化蛋白(CFP)的单特异性抗体被插入电泳板上的第一位置。来自待测对象的体液被放置在板上的第二位置。在位置上施加电位,其中阳极邻近包含血清的部分,而阴极邻近包含抗体的部分。囊性纤维化蛋白的存在由一个或多个沉淀区指示,在这些沉淀区中,由于施加的电势引起的运动,体液蛋白与抗体相遇。沉淀区在第一和第二位置之间的相对位置或沉淀区的面积表明了囊性纤维化蛋白的浓度。还公开了产生纯化的囊性纤维化蛋白抗体和纯化囊性纤维化蛋白本身的方法。

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