구제역 O-Cathay 지역형에 대한 방어단백질을 발현하는 구제역바이러스
    46.
    发明公开
    구제역 O-Cathay 지역형에 대한 방어단백질을 발현하는 구제역바이러스 有权
    FOOT AND MOUTH DISEASE VIRUS EXPRESSING P1-PROTECTIVE ANTIGEN OF O-CATHAY TOPOTYPE

    公开(公告)号:KR1020130114946A

    公开(公告)日:2013-10-21

    申请号:KR1020120037407

    申请日:2012-04-10

    Abstract: PURPOSE: Foot and mouth disease virus expressing defensive protein against foot and mouth disease of O-Cathay topotype is provided to be made into a vaccine, defend against O-Cathy topotype and produce a large amount of antibodies capable of defense within 1-2 weeks by single inoculation. CONSTITUTION: A plasmid has a base sequence like a sequence number 1. In the plasmid, a defensive gene against foot and mouth disease of O-Cathay topotype is inserted. Foot and mouth disease O serotype Cathay structural protein is expressed and produced from the plasmid.

    Abstract translation: 目的:提供表达O-Cathay拓扑型口蹄疫防御性蛋白质的口蹄疫病毒,制成疫苗,捍卫O-Cathy拓扑型,并在1-2周内产生大量能够防御的抗体 通过单次接种。 构成:质粒具有序列号1的碱基序列。在质粒中插入了针对O-Cathay拓扑型的口蹄疫的防御基因。 口蹄疫O血清型国泰结构蛋白由质粒表达和产生。

    돼지콜레라 바이러스 Erns 단백질 및 이에 특이적으로반응하는 단클론항체를 이용한 돼지콜레라 항체 감별진단방법
    49.
    发明公开
    돼지콜레라 바이러스 Erns 단백질 및 이에 특이적으로반응하는 단클론항체를 이용한 돼지콜레라 항체 감별진단방법 有权
    SWINE FEVER VIRUS ERNS蛋白质和筛选和检测与其相似的SWINE FEVER病毒抗体的方法

    公开(公告)号:KR1020070116382A

    公开(公告)日:2007-12-10

    申请号:KR1020060050357

    申请日:2006-06-05

    Abstract: A method for screening and detecting a swine fever virus antibody is provided to easily screen and diagnose infected swine fever virus antibody by using a monoclonal antibody specifically reacting with a recombinant swine fever virus Erns protein and secure constant sensitivity regardless of all genotypes of the swine fever virus when using all three kinds of recombinant protein. A recombinant swine fever virus Erns is prepared by expressing a gene encoding three Erns proteins among swine fever viruses having various genotypes using baculovirus. A method for preparing a monoclonal antibody specifically reacting to the Erns comprises the steps of: (a) constructing a swine fever virus LOM strain-derived Erns recombinant gene using a baculovirus expression system; and (b) producing the monoclonal antibody using the recombinant Erns protein. A method for screening and detecting a swine fever virus antibody comprises the steps of: (a) mixing three kinds of Erns recombinant proteins at proper concentration to prepare an antigen cocktail; (b) after diluting the antigen cocktail into a coating buffer solution, pouring it in a plate to be absorbed into the plate; (c) washing the recombinant antigen not-absorbed into the plate to remove it; (d) adding a sample to be tested to the plat to allow the reaction; (e) washing the sample to be tested not specifically bound to the recombinant Erns antigen protein absorbed into the plate to remove it; (f) adding a monoclonal antibody not being bound to the enzyme but being specifically reacted to the Erns protein to allow the reaction; (g) washing the monoclonal antibody not being bound to the recombinant Erns antigen protein absorbed into the plate to remove it; and (h) adding a substrate reacting with the enzyme to determine the swine fever virus infection.

    Abstract translation: 提供了一种筛选和检测猪瘟病毒抗体的方法,通过使用与重组猪瘟病毒Erns蛋白特异性反应的单克隆抗体轻松筛选和诊断感染的猪瘟病毒抗体,无论猪瘟的所有基因型如何 使用全部三种重组蛋白的病毒。 通过使用杆状病毒在具有各种基因型的猪瘟病毒中表达编码三种Erns蛋白质的基因来制备重组猪瘟病毒Erns。 制备与Erns特异性反应的单克隆抗体的方法包括以下步骤:(a)使用杆状病毒表达系统构建猪瘟病毒LOM菌株衍生的Erns重组基因; 和(b)使用重组Erns蛋白产生单克隆抗体。 筛选和检测猪瘟病毒抗体的方法包括以下步骤:(a)以适当浓度混合三种Erns重组蛋白以制备抗原混合物; (b)将抗原混合物稀释到涂布缓冲溶液中后,将其倒入板中吸收到板中; (c)将未吸收的重组抗原洗涤到板中以除去它; (d)将待测试样品加入平板以允许反应; (e)洗涤待测试的样品,未特异性地结合到吸收到板中的重组Erns抗原蛋白质以除去它; (f)加入未结合酶的单克隆抗体,但与Erns蛋白特异性反应以进行反应; (g)洗涤未结合到吸附到板中的重组Erns抗原蛋白的单克隆抗体以除去它; 和(h)加入与酶反应的底物以确定猪瘟病毒感染。

    유전자재조합 바큘로바이러스 및 이에 의한 재조합 돼지전염성위장염바이러스 스파이크 단백질을 이용한 돼지전염성위장염바이러스 항체 검출을 위한 효소면역 검사방법

    公开(公告)号:KR100267744B1

    公开(公告)日:2000-11-01

    申请号:KR1019980000446

    申请日:1998-01-10

    Abstract: PURPOSE: Provided are a genetic recombinant baculovirus and a recombinant spike protein of transmissible gastroenteritis virus(TGEV) manufactured therefrom. And a monoclonal antibody capture enzyme linked immunosorbent assay for detecting the antibody of TGEV using the same protein is also provided, thereby the antibody of TGEV can be rapidly detected. CONSTITUTION: The recombinant spike protein of TGEV is produced by the steps of: isolating and identifying TGEV from pigs died of diarrhea; analyzing the nucleotide sequence of spike protein of TGEV; inserting the TGEV spike gene into the baculovirus gene to produce a recombinant baculovirus(KFCC-11015); infecting the recombinant baculovirus into SF9 cells to express TGEV spike protein. The antibody of TGEV is produced by inoculating the expressed recombinant TGEV spike protein into Guinea pigs. The monoclonal antibody capture enzyme linked immunosorbent assay using TGEV spike protein that is produced from the recombinant baculovirus(KFCC-11015) in Guinea pigs as an antigen is used in detecting the neutralizing antibody of TGEV.

    Abstract translation: 目的:提供遗传重组杆状病毒和由其制备的传染性胃肠炎病毒(TGEV)的重组穗蛋白。 还提供了使用相同蛋白质检测TGEV抗体的单克隆抗体捕获酶联免疫吸附测定法,从而可以快速检测TGEV抗体。 构成:TGEV的重组穗蛋白是通过以下步骤制备的:从腹泻死亡的猪中分离和鉴定TGEV; 分析TGEV刺突蛋白的核苷酸序列; 将TGEV刺突基因插入杆状病毒基因以产生重组杆状病毒(KFCC-11015); 将重组杆状病毒感染到SF9细胞中以表达TGEV穗蛋白。 通过将表达的重组TGEV穗蛋白接种到豚鼠中来产生TGEV抗体。 使用从作为抗原的豚鼠中的重组杆状病毒(KFCC-11015)产生的TGEV尖峰蛋白的单克隆抗体捕获酶联免疫吸附测定用于检测TGEV的中和抗体。

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