公开(公告)号：KR1020040022247A

公开(公告)日：2004-03-12

申请号：KR1020010082714

申请日：2001-12-21

Applicant: 대한민국(농림축산식품부 농림축산검역본부장)

Inventor： 권창희 ,  권병준 ,  고영준 ,  이세영 ,  김인중 ,  주이석

IPC: A61K39/12

Abstract: PURPOSE: A method of diagnosing vesicular stomatitis by performing an ELISA method using the recombinant envelope glycoprotein antigen of vesicular stomatitis virus(VSV) and monoclonal antibodies thereon is provided. Therefore, it permits quick, exact and specific antibody detection of the VSV and thus exact diagnosis of vesicular stomatitis through the detection. CONSTITUTION: The diagnosing method for vesicular stomatitis is achieved through a VSV detection method consisting of: attaching monoclonal antibodies against an envelope glycoprotein antigen of VSV on a solid supporter; binding the envelope glycoprotein antigen to the monoclonal antibodies attached on the solid supporter in the first step; reacting a sample containing an antibody against the envelope glycoprotein antigen with the envelope glycoprotein antigen of the second step; reacting a secondary antibody selected from the group consisting of a conjugate antibody attached with enzyme and a conjugate antibody attached with a luminescent material with the antibody of the third step.

Abstract translation: 目的：提供使用水泡性口炎病毒（VSV）的重组包膜糖蛋白抗原及其单克隆抗体进行ELISA方法诊断水泡性口炎的方法。 因此，它可以快速，精确和特异性地检测VSV，从而通过检测确定水泡性口炎的诊断。 构成：水泡性口炎的诊断方法是通过VSV检测方法实现的，该方法包括：将固定支持物上VSV的包膜糖蛋白抗原的单克隆抗体连接起来; 在第一步中将包膜糖蛋白抗原与附着在固体支持物上的单克隆抗体结合; 使含有针对包膜糖蛋白抗原的抗体的样品与第二步的包膜糖蛋白抗原反应; 使选自由酶附着的结合抗体和附着有发光材料的缀合物抗体的第二抗体与第三步骤的抗体反应。

公开(公告)号：KR100331177B1

公开(公告)日：2002-04-06

申请号：KR1019990025161

申请日：1999-06-29

Applicant: 대한민국(농림축산식품부 농림축산검역본부장)

Inventor： 권창희 ,  권병준 ,  우승룡 ,  김종만 ,  조준형

IPC: C12Q1/70

Abstract: 본발명은돼지유행성설사병바이러스의진단방법및 진단키트에관한것으로서, 보다상세하게는돼지전염성설사질병의원인체인돼지유행성설사병바이러스항체와면역학적으로결합성이있는시료내의돼지유행성설사병바이러스항원의존재를경제적이며간편하게진단할수 있는방법및 그에유용한진단키트에관한것이다.

公开(公告)号：KR1020030052688A

公开(公告)日：2003-06-27

申请号：KR1020010082715

申请日：2001-12-21

Applicant: 대한민국(농림축산식품부 농림축산검역본부장)

Inventor： 권창희 ,  권병준 ,  고영준 ,  이세영 ,  주이석

IPC: G01N33/68

Abstract: PURPOSE: A VP7 antigen of African horse sickness virus(AHSV) and a diagnostic method of African horse sickness(AHS) using a monoclonal antibody therefor are provided, thereby rapidly and accurately diagnosing AHSV. CONSTITUTION: A diagnostic method of African horse sickness(AHS) using a monoclonal antibody to VP7 antigen of African horse sickness virus(AHSV) comprises the steps of: (1) adhering a monoclonal antibody for VP7 antigen of African horse sickness virus(AHSV) to a solid support; (2) binding the VP7 antigen of AHSV with the monoclonal antibody adhered to the solid support; (3) reacting a sample containing an antibody for a VP7 protein with the VP7 antigen of AHSV; (4) reacting a secondary antibody selected from the group consisting of an enzyme conjugated antibody, a radioactive material conjugated antibody and a fluorescent material conjugated antibody, with the antibody of the step 3; and (5) quantifying the antibody in the sample, wherein the monoclonal antibody for VP7 antigen of African horse sickness virus(AHSV) is produced from a hybridoma cell(KCTC 10136BP).

Abstract translation: 目的：提供非洲马病病毒（AHSV）的VP7抗原和使用其单克隆抗体的非洲马病诊断方法（AHS），从而快速准确地诊断AHSV。 构成：使用非洲马病病毒（AHSV）的VP7抗原单克隆抗体的非洲马病诊断方法（AHS）包括以下步骤：（1）将非洲马病病毒（AHSV）VP7抗原的单克隆抗体 坚定的支持; （2）将AHSV的VP7抗原与附着在固体支持物上的单克隆抗体结合; （3）将含有VP7蛋白抗体的样品与AHSV的VP7抗原反应; （4）将选自酶结合抗体，放射性物质缀合抗体和荧光物质缀合抗体的二抗与步骤3的抗体反应; 和（5）定量样品中的抗体，其中非洲马病病毒（AHSV）的VP7抗原单克隆抗体由杂交瘤细胞（KCTC 10136BP）产生。

公开(公告)号：KR100267748B1

公开(公告)日：2000-10-16

申请号：KR1019980017349

申请日：1998-05-14

Applicant: 대한민국(농림축산식품부 농림축산검역본부장)

Inventor： 권창희 ,  권병준

IPC: C12N7/02

Abstract: PURPOSE: A method for purifying porcine infectious coronavirus is provided, thereby the porcine infectious coronavirus can be simply and rapidly purified without losing its activity, so that it can be used in producing vaccines or diagnosis kits. CONSTITUTION: The method for purifying porcine infectious coronavirus comprises the steps of: packing the column with crosslinked polysaccharides or sulfate ester of cellulose; washing the column with TEN buffer solution(pH 7.5) consisting of 10mM of Tris, 1mM of EDTA and 100mM of sodium chloride; homogenizing the column with TEN buffer solution; passing the porcine infectious coronavirus containing solution through the column to adsorb it to the column; washing the column with TEN buffer solution; and eluting the porcine infectious coronavirus with TEN buffer solution(pH 7.5) consisting of 10mM of Tris, 1mM of EDTA and 1.0 to 3.0M of sodium chloride.

Abstract translation: 目的：提供猪传染性冠状病毒的纯化方法，可以简单，快速地纯化猪感染性冠状病毒，而不会失去活性，可用于生产疫苗或诊断试剂盒。 构成：猪传染性冠状病毒的纯化方法包括以下步骤：用交联的多糖或纤维素硫酸酯包装柱; 用10mM Tris，1mM EDTA和100​​mM氯化钠组成的TEN缓冲溶液（pH7.5）洗涤柱子; 用TEN缓冲溶液均质柱; 将含有感染性冠状病毒的溶液通过柱吸附到柱上; 用TEN缓冲溶液洗涤柱; 并用10mM Tris，1mM EDTA和1.0-3.0M氯化钠组成的TEN缓冲溶液（pH7.5）洗脱猪感染性冠状病毒。

公开(公告)号：KR1020010037612A

公开(公告)日：2001-05-15

申请号：KR1019990045242

申请日：1999-10-19

Applicant: 대한민국(농림축산식품부 농림축산검역본부장)

Inventor： 우승룡 ,  김종만 ,  이지연 ,  권창희 ,  오진식 ,  권병준 ,  김종염

IPC: A23K1/18

CPC classification number: A23K50/00 ,  A23K10/20 ,  A23K40/10

Abstract: PURPOSE: A feed additive is provided to prevent and treat the pig colon bacillus diarrhea by using dried yolk powder having an idioantibody. CONSTITUTION: A testing vaccine manufactured by using a cilium antigen of the colon bacillus is inoculated on a layer and immunized. The eggs are disinfected with alcohol and the egg yolk is aseptically collected in an Erlenmeyer Flask. The collected yolk is injected into a powder dryer to gather yolk powder. The injecting temperature of the powder dryer is 140deg.C and the releasing temperature is 72deg.C. The dried powder weight per 1ml vol and the moisture content of the egg yolk are 0.38g and 2%, respectively. The value of an antibody is rarely changed before and after the drying.

Abstract translation: 目的：提供饲料添加剂，通过使用具有不良反应的干燥的蛋黄粉来预防和治疗猪大肠杆菌腹泻。 构成：将通过使用大肠杆菌的纤毛抗原制造的测试疫苗接种在一层上并免疫。 鸡蛋用酒精消毒，蛋黄被无菌地收集在锥形瓶中。 将收集的蛋黄注入粉末干燥器中以收集蛋黄粉末。 粉末干燥机的注射温度为140℃，脱模温度为72℃。 每1ml体积的干燥粉末重量和蛋黄的水分含量分别为0.38g和2％。 干燥前后抗体的值很少变化。

公开(公告)号：KR100449908B1

公开(公告)日：2004-09-22

申请号：KR1020010082714

申请日：2001-12-21

Applicant: 대한민국(농림축산식품부 농림축산검역본부장)

Inventor： 권창희 ,  권병준 ,  고영준 ,  이세영 ,  김인중 ,  주이석

IPC: A61K39/12

Abstract: PURPOSE: A method of diagnosing vesicular stomatitis by performing an ELISA method using the recombinant envelope glycoprotein antigen of vesicular stomatitis virus(VSV) and monoclonal antibodies thereon is provided. Therefore, it permits quick, exact and specific antibody detection of the VSV and thus exact diagnosis of vesicular stomatitis through the detection. CONSTITUTION: The diagnosing method for vesicular stomatitis is achieved through a VSV detection method consisting of: attaching monoclonal antibodies against an envelope glycoprotein antigen of VSV on a solid supporter; binding the envelope glycoprotein antigen to the monoclonal antibodies attached on the solid supporter in the first step; reacting a sample containing an antibody against the envelope glycoprotein antigen with the envelope glycoprotein antigen of the second step; reacting a secondary antibody selected from the group consisting of a conjugate antibody attached with enzyme and a conjugate antibody attached with a luminescent material with the antibody of the third step.

Abstract translation: 目的：提供一种使用水疱性口炎病毒（VSV）的重组包膜糖蛋白抗原和单克隆抗体进行ELISA方法来诊断水疱性口炎的方法。 因此，它可以快速，准确和特异地检测VSV的抗体，从而通过检测来精确诊断水疱性口炎。 组成：水泡性口炎的诊断方法通过VSV检测方法实现，该方法包括：将抗VSV的包膜糖蛋白抗原的单克隆抗体附着在固体支持物上; 在第一步中将包膜糖蛋白抗原结合至附着于固体载体上的单克隆抗体; 使含有抗包膜糖蛋白抗原的抗体的样品与第二步的包膜糖蛋白抗原反应; 使选自附着有酶的缀合物抗体和附着有荧光物质的缀合物抗体的第二抗体与第三步骤的抗体反应。

公开(公告)号：KR100430935B1

公开(公告)日：2004-05-14

申请号：KR1020010082975

申请日：2001-12-21

Applicant: 대한민국(농림축산식품부 농림축산검역본부장)

Inventor： 권창희 ,  권병준 ,  고영준 ,  나진주 ,  김원일 ,  이세영 ,  주이석

IPC: C12N15/33

Abstract: PURPOSE: Diagnostic methods of foot-and-mouth disease using a recombinant 3ABC non-structural protein expressed in E. coli and a monoclonal antibody is provided, thereby more rapidly and accurately diagnosing the foot-and-mouth disease than the prior methods. CONSTITUTION: A gene encoding a recombinant 3ABC non-structural protein derived from Korean foot-and-mouth disease virus O/SKR/2000 has the nucleotide sequence of SEQ ID NO: 1. The recombinant 3ABC non-structural protein is expressed from a recombinant E. coli transformed with a recombinant vector containing the recombinant 3ABC non-structural protein gene of SEQ ID NO: 1. A hybridoma cell line 3F-11(KCTC 10138BP) is prepared by introducing the recombinant 3ABC non-structural protein expressed in E. coli into an animal, collecting an immunized cell from the animal and fusing the immunized cell with a cancer cell. A monoclonal antibody is produced from the hybridoma cell line 3F-11(KCTC 10138BP). A diagnostic method of foot-and-mouth disease comprises the steps of: (1) diluting the recombinant 3ABC non-structural protein in a coating buffer solution and pouring the dilution on a plate; (2) reacting the testing serum with the plate; (3) reacting the 3ABC non-structural protein specific monoclonal antibody with the serum; (4) reacting a 3ABC non-structural protein specific monoclonal antibody binding conjugate with the monoclonal antibody; and (5) measuring intensity of the enzyme reaction, fluorescence reaction or radiation reaction with the conjugate.

Abstract translation: 目的：提供使用在大肠杆菌中表达的重组3ABC非结构蛋白和单克隆抗体的口蹄疫诊断方法，从而比现有方法更快速和更准确地诊断口蹄疫。 构成：编码来源于韩国口蹄疫病毒O / SKR / 2000的重组3ABC非结构蛋白的基​​因具有SEQ ID NO：1的核苷酸序列。重组3ABC非结构蛋白由重组 用含有SEQ ID NO：1的重组3ABC非结构蛋白基因的重组载体转化大肠杆菌。通过引入在E.coli中表达的重组3ABC非结构蛋白制备杂交瘤细胞系3F-11（KCTC 10138BP） 将大肠杆菌导入动物体内，从动物体内收集免疫细胞，并将免疫细胞与癌细胞融合。 从杂交瘤细胞系3F-11（KCTC 10138BP）产生单克隆抗体。 口蹄疫诊断方法包括以下步骤：（1）将重组3ABC非结构蛋白稀释于包被缓冲液中，并将稀释液倒入板中; （2）使测试血清与平板反应; （3）使3ABC非结构蛋白特异性单克隆抗体与血清反应; （4）使3ABC非结构蛋白特异性单克隆抗体结合缀合物与单克隆抗体反应; 和（5）测量酶反应的强度，与偶联物的荧光反应或辐射反应。

公开(公告)号：KR1020030052857A

公开(公告)日：2003-06-27

申请号：KR1020010082975

申请日：2001-12-21

Applicant: 대한민국(농림축산식품부 농림축산검역본부장)

Inventor： 권창희 ,  권병준 ,  고영준 ,  나진주 ,  김원일 ,  이세영 ,  주이석

IPC: C12N15/33

CPC classification number: C07K14/005 ,  C07K16/1009 ,  C07K2317/14 ,  C12N5/163 ,  C12N15/70 ,  C12N2770/32131 ,  G01N33/56983 ,  G01N33/577 ,  G01N2333/09

Abstract: PURPOSE: Diagnostic methods of foot-and-mouth disease using a recombinant 3ABC non-structural protein expressed in E. coli and a monoclonal antibody is provided, thereby more rapidly and accurately diagnosing the foot-and-mouth disease than the prior methods. CONSTITUTION: A gene encoding a recombinant 3ABC non-structural protein derived from Korean foot-and-mouth disease virus O/SKR/2000 has the nucleotide sequence of SEQ ID NO: 1. The recombinant 3ABC non-structural protein is expressed from a recombinant E. coli transformed with a recombinant vector containing the recombinant 3ABC non-structural protein gene of SEQ ID NO: 1. A hybridoma cell line 3F-11(KCTC 10138BP) is prepared by introducing the recombinant 3ABC non-structural protein expressed in E. coli into an animal, collecting an immunized cell from the animal and fusing the immunized cell with a cancer cell. A monoclonal antibody is produced from the hybridoma cell line 3F-11(KCTC 10138BP). A diagnostic method of foot-and-mouth disease comprises the steps of: (1) diluting the recombinant 3ABC non-structural protein in a coating buffer solution and pouring the dilution on a plate; (2) reacting the testing serum with the plate; (3) reacting the 3ABC non-structural protein specific monoclonal antibody with the serum; (4) reacting a 3ABC non-structural protein specific monoclonal antibody binding conjugate with the monoclonal antibody; and (5) measuring intensity of the enzyme reaction, fluorescence reaction or radiation reaction with the conjugate.

Abstract translation: 目的：提供使用在大肠杆菌中表达的重组3ABC非结构蛋白和单克隆抗体的口蹄疫的诊断方法，从而比现有方法更快速和准确地诊断口蹄疫。 构成：编码来自韩国口蹄疫病毒O / SKR / 2000的重组3ABC非结构蛋白的基​​因具有SEQ ID NO：1的核苷酸序列。重组体3ABC非结构蛋白由重组体 用含有SEQ ID NO：1的重组3ABC非结构蛋白基因的重组载体转化大肠杆菌。通过引入在E中表达的重组3ABC非结构蛋白来制备杂交瘤细胞系3F-11（KCTC 10138BP）。 将大肠杆菌转化成动物，从动物中收集免疫的细胞并将免疫的细胞与癌细胞融合。 从杂交瘤细胞系3F-11（KCTC 10138BP）产生单克隆抗体。 口蹄疫的诊断方法包括以下步骤：（1）在包被缓冲溶液中稀释重组体3ABC非结构蛋白，并将稀释液倒在平板上; （2）使测试血清与板反应; （3）使3ABC非结构蛋白特异性单克隆抗体与血清反应; （4）使3ABC非结构蛋白特异性单克隆抗体结合缀合物与单克隆抗体反应; 和（5）测量酶反应的强度，荧光反应或与缀合物的辐射反应。

公开(公告)号：KR1019990085154A

公开(公告)日：1999-12-06

申请号：KR1019980017349

申请日：1998-05-14

Applicant: 대한민국(농림축산식품부 농림축산검역본부장)

Inventor： 권창희 ,  권병준

IPC: C12N7/02

Abstract: 본 발명은 주요 돼지 전염성 질병의 원인체로 돼지 코로나바이러스군인 유행성 설사병 바이러스, 전염성 위장염 바이러스 및 호흡기 코로나바이러스를 신속하고, 간편하게 고역가로 정제하는 방법에 관한 것으로, 본 발명에 의해 정제된 바이러스는 면역제제 작성이나 ELISA법, Dip-stick법, dot blot법 등에 적용되어 바이러스의 진단에 이용될 수 있으며, 고효능의 예방약 생산 및 야외에서 손쉽게 적용할 수 있는 진단키트의 생산에도 사용될 수 있다.

公开(公告)号：KR100522086B1

公开(公告)日：2005-11-09

申请号：KR1020010082715

申请日：2001-12-21

Applicant: 대한민국(농림축산식품부 농림축산검역본부장)

Inventor： 권창희 ,  권병준 ,  고영준 ,  이세영 ,  주이석

IPC: G01N33/68

Abstract: 본 발명은 아프리카 마역 바이러스를 검출하여, 아프리카 마역을 진단하는 방법에 관한 것으로, 더욱 상세하게는 아프리카 마역바이러스에 감염된 혈청 내에 존재하는 VP7에 대한 항체를 아프리카 마역바이러스의 VP7 항원 및 상기 VP7 항원에 대한 모노클로날 항체를 이용하는 ELISA법으로 아프리카 마역 항체를 검출함으로써, 아프리카 마역을 진단하는 방법에 관한 것이다.