5 ID 50/ml. Viruses are concentrated by ultrafiltration by 10-20-fold, lipid envelope is separated by treatment with ether in cold and the end product that is peptide (molecular mass is 24-26 kDa) carrying group-specific antigen determinants is obtained. After the concentration stage viral material can be subjected for purification by high-speed centrifugation and ultracentrifugation additionally. After separation of lipid envelope obtained antigen is purified by affinity chromatography additionally. In this case the end product is immunoelectrophoretically pure peptide. Obtained cultural antigen is used for kit making for identification of antigen of equine infectious anemia virus. Kits for identification of antibodies are designated for diagnosis of equine infectious anemia in RDP or IFA. Kit for identification of antigen is designated for titration of antigen of equine infectious anemia virus in the process of culturing. Kit for identification of antibodies in RDP has cultural antigen and specific precipitating serum. Kit for identification of antibodies in IFA has cultural antigen for immobilization on solid carrier, polystyrene plate and antispecies immunoglobulin class G (Ig G) conjugated with horse radish peroxidase. Kit for identification of antigen has cultural antigen for immobilization on solid carrier, polystyrene plate and Ig G to equine infectious anemia virus conjugated with horse radish peroxidase. Kits for IFA have gelatin, substrate for peroxidase reaction carrying out, detergent and buffer solutions also. Kits can contain positive and negative controls also. EFFECT: enhanced sensitivity, standard specification and specificity of cultural antigen and kits for identification of antibodies and antigen. 18 cl, 6 ex"/> METHOD OF PREPARING CULTURAL ANTIGEN FROM EQUINE INFECTIOUS ANEMIA VIRUS AND KIT FOR ANTIBODY OR ANTIGEN OF EQUINE INFECTIOUS ANEMIA VIRUS
首页> 外国专利> METHOD OF PREPARING CULTURAL ANTIGEN FROM EQUINE INFECTIOUS ANEMIA VIRUS AND KIT FOR ANTIBODY OR ANTIGEN OF EQUINE INFECTIOUS ANEMIA VIRUS

METHOD OF PREPARING CULTURAL ANTIGEN FROM EQUINE INFECTIOUS ANEMIA VIRUS AND KIT FOR ANTIBODY OR ANTIGEN OF EQUINE INFECTIOUS ANEMIA VIRUS

机译:从马传染性贫血病毒中制备文化抗原的方法和用于马传染性贫血病毒的抗体或抗原的试剂盒

摘要

FIELD: biotechnology, veterinary virology. SUBSTANCE: method involves the use of the novel strain of equine infectious anemia virus N "3-K-VNIITIBP-VIEV" for antigen preparing. Strain is grown in horse embryo skin and/or muscle, or lung, and/or kidney cells up to accumulation of viruses at titer 105 ID 50/ml. Viruses are concentrated by ultrafiltration by 10-20-fold, lipid envelope is separated by treatment with ether in cold and the end product that is peptide (molecular mass is 24-26 kDa) carrying group-specific antigen determinants is obtained. After the concentration stage viral material can be subjected for purification by high-speed centrifugation and ultracentrifugation additionally. After separation of lipid envelope obtained antigen is purified by affinity chromatography additionally. In this case the end product is immunoelectrophoretically pure peptide. Obtained cultural antigen is used for kit making for identification of antigen of equine infectious anemia virus. Kits for identification of antibodies are designated for diagnosis of equine infectious anemia in RDP or IFA. Kit for identification of antigen is designated for titration of antigen of equine infectious anemia virus in the process of culturing. Kit for identification of antibodies in RDP has cultural antigen and specific precipitating serum. Kit for identification of antibodies in IFA has cultural antigen for immobilization on solid carrier, polystyrene plate and antispecies immunoglobulin class G (Ig G) conjugated with horse radish peroxidase. Kit for identification of antigen has cultural antigen for immobilization on solid carrier, polystyrene plate and Ig G to equine infectious anemia virus conjugated with horse radish peroxidase. Kits for IFA have gelatin, substrate for peroxidase reaction carrying out, detergent and buffer solutions also. Kits can contain positive and negative controls also. EFFECT: enhanced sensitivity, standard specification and specificity of cultural antigen and kits for identification of antibodies and antigen. 18 cl, 6 ex
机译:领域:生物技术,兽医病毒学。物质:该方法涉及使用马传染性贫血病毒N“ 3-K-VNIITIBP-VIEV”的新型菌株制备抗原。菌株在马胚的皮肤和/或肌肉,或肺和/或肾细胞中生长,直至病毒积累,滴度为10 5 ID 50 / ml。通过超滤将病毒浓缩10-20倍,在寒冷条件下通过乙醚处理分离脂质被膜,得到的终产物是带有基团特异性抗原决定簇的肽(分子量为24-26 kDa)。在浓缩阶段之后,可以通过高速离心和超速离心对病毒物质进行纯化。分离脂质包膜后,另外通过亲和色谱法纯化获得的抗原。在这种情况下,最终产物是免疫电泳纯肽。获得的培养抗原用于试剂盒的鉴定,以鉴定马传染性贫血病毒。指定了用于鉴定抗体的试剂盒,用于诊断RDP或IFA中的马传染性贫血。指定用于抗原鉴定的试剂盒,用于在培养过程中滴定马传染性贫血病毒的抗原。用于鉴定RDP中抗体的试剂盒具有培养抗原和特定沉淀血清。用于在IFA中鉴定抗体的试剂盒具有用于固定在固体载体,聚苯乙烯板上的培养抗原,以及与辣根过氧化物酶偶联的G类抗球蛋白免疫球蛋白(Ig G)。用于鉴定抗原的试剂盒具有用于固定在固体载体,聚苯乙烯平板和Ig G上的培养抗原,以马与辣根过氧化物酶偶联的传染性贫血病毒。 IFA的试剂盒包括明胶,进行过氧化物酶反应的底物,去污剂和缓冲溶液。试剂盒也可以包含阳性和阴性对照。效果:提高了培养抗原的灵敏度,标准规格和特异性,以及用于鉴定抗体和抗原的试剂盒。 18 cl,6前

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