首页> 外国专利> METHOD FOR PRODUCING ERYTHROCYTE antibody OVISNOGO DIAGNOSTICUM for the reaction of indirect hemagglutination (IHA) to indicate the OVISNOGO antigen in biomaterials

METHOD FOR PRODUCING ERYTHROCYTE antibody OVISNOGO DIAGNOSTICUM for the reaction of indirect hemagglutination (IHA) to indicate the OVISNOGO antigen in biomaterials

机译:产生红细胞抗体OVISNOGO DIAGNOSTICUM的方法用于间接血凝反应(IHA)以指示生物材料中的OVISNOGO抗原

摘要

FIELD: biotechnologies.;SUBSTANCE: invention proposes a method for obtaining erythrocytic antibody diagnosticum for indirect hemagglutination reaction (IHAR) to indicate ovis antibody in biomaterial. The method is implemented by preparation of stabilised erythrocytes with further sensibilisation by positive ovis serum. In order to manufacture erythrocytic antibody diagnosticum, positive ovis serum for sensibilisation of stabilised erythrocytes is diluted in the ratio of 1:200-1:400, inactivated at 60°C during 30 minutes, and formalinised erythrocytes are sensibilised in the following ratio: one volume of 10% suspension of erythrocytes, one volume of positive ovis serum in the working dilution of (1:200-1:400), which is inactivated at 60°C during 30 minutes. Then, one volume of fresh water solution (0.1-0.11%) of water soluble alizarine blue indicator is added. Mixture is shaken and exposed during 60 minutes at 45°C, thus being stirred from time to time.;EFFECT: method allows obtaining erythrocytic ovis antibody diagnosticum having high activity and specificity.;1 tbl
机译:发明领域:本发明提出了一种获得用于间接血凝反应(IHAR)以指示生物材料中的羊抗体的红细胞抗体诊断物的方法。该方法通过制备稳定的红血球并通过正羊血清进一步敏化来实现。为了制造诊断性红细胞抗体,将用于稳定化红细胞敏化的阳性羊血清以1:200-1:400的比例稀释,在60°C下30分钟灭活,然后以以下比例使福尔马林化的红细胞敏化:体积的10%红细胞悬液,一体积的正羊血清在(1:200-1:400)的工作稀释液中,在60°C灭活30分钟。然后,加入一体积的水溶性茜素蓝指示剂的淡水溶液(0.1-0.11%)。混合物在45°C下摇动和暴露60分钟,因此不时进行搅拌。效果:该方法可以得到具有高活性和特异性的诊断性红细胞羊抗体。

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