Abstract:
The present invention relates to a recombinant adenovirus expressing a rabies virus gene and a vaccine composition for preventing or treating rabies comprising the same. The recombinant adenovirus according to the present invention, which is a recombinant virus of nucleotide sequences coding G protein and N protein of the rabies virus isolated from the country, effectively expresses G protein and N protein of the rabies virus and has a proliferation ability suitable for the use as a vaccine strain, and thus is suitable in mass production thereof. Further, the present invention has improved stability as compared with the exiting vaccine and thus can be used for oral administration, and has excellent ability to defend against the rabies virus at the time of vaccination.
Abstract:
본 발명은 소 면역글로불린 지(Immunoglobulin G; 이하 "IgG"라 한다)의 에프씨(Crystallized Fragment; 이하 "Fc"라 한다) 도메인의 세포 표면 발현용 벡터, 상기 벡터에 의해 형질전환된 숙주세포 및 상기 숙주세포를 이용한 소 질병 관련 바이러스에 대한 백신의 제조방법에 관한 것이다. 본 발명에 따른 숙주세포에 바이러스를 증식시키는 경우 바이러스 외피에 Fc가 포함됨으로써 다양한 소 질병 관련 바이러스에 대하여 면역능이 우수한 백신을 손쉽게 생산할 수 있도록 해준다. 소 IgG, Fc 유전자, 표면 발현, 벡터
Abstract:
The present invention relates to the recombinant rabies virus rERAG333Glu and a vaccine composition containing the same for preventing rabies. The recombinant rabies virus rERAG333Glu according to the present invention is a recombinant virus strain where the 333rd amino acid of G protein is replaced by glutamic acid. When manufacturing a vaccine from the virus, the vaccine has an excellent amount of virus so as to be suitable for mass-production, and has improved stability compared with the existing vaccines so as to be used for oral administration. Therefore, it can produce effects of solving problems of the existing rabies virus vaccines and being used as an effective vaccine for preventing rabies virus.
Abstract:
본 발명은 바이러스에 대한 필터의 효력평가장치 및 효력평가방법에 관한 것이다. 본 발명의 바이러스에 대한 필터의 효력평가장치는 외부로부터 유입되는 바이러스를 수용하는 제1무균상챔버와, 제1무균상챔버와 연통하게 설치되어 제1무균상챔버로부터 공기를 흡입하여 제1무균상챔버의 공기중의 바이러스량을 검출하도록 한 제1포집부로 이루어진 제1검출수단; 상기 제1검출수단의 제1무균상챔버와 연통하는 제2검출수단의 제2무균상챔버와의 사이에 설치되어 제1무균상챔버로부터 제2무균상챔버로 유동하는 공기를 필터링하여 바이러스를 걸러내도록 한 필터수단; 및 상기 필터수단을 통해서 제1무균상챔버와 연통하게 설치되며 필터수단에 의해 필터링된 제1무균상챔버의 공기를 유입하여 수용하도록 한 제2무균상챔버와, 제2무균상챔버의 공기를 흡입함으로써 제1무균상챔버로부터 필터수단을 경유한 공기중의 바이러스를 포집하여 제2무균상챔버의 공기중의 바이러스량을 검출하도록 한 제2포집부로 이루어진 제2검출수단을 포함하여 구성된다. 본 발명에 의해, 다양한 바이러스에 대한 필터의 효력평가가 가능하고 음압공조기에 의해 생체인 실험동물을 대상으로 과학적이고 손쉽게 필터의 효력평가도 가능하여 편리한 효과가 있다.
Abstract:
PURPOSE: A scFv gene of monoclonal antibody 4G31 and a recombinant protein expressing the same are provided to neutralize RAV and to reduce and diagnose rabies virus. CONSTITUTION: A 4G31 scFv(single chain variable fragment antibody) gene which specifically neutralizes rabies virus has an amino acid sequence and a base of sequence number 16. The 4G31 scFv gene is a 4G31 monoclonal antibody containing a gene encoding a heavy chain variable region(VH) and a light chain variable region(VL). An expression vector expresses the 4G31 scFv gene. A recombinant protein is prepared by expressingthe 4G31 scFv gene in E.coli using the expression vector. A therapeutic agent for rabies virus contains the recombinant protein expressed from the 4G31 scFv gene.
Abstract:
A kit and a method for diagnosing a porcine epidemic diarrhea virus antigen are provided to diagnose the antigen conveniently and rapidly without a special testing equipment in a farm or a laboratory field. A kit for diagnosing a porcine epidemic diarrhea virus antigen is characterized in that a conjugate of a monoclonal antibody 6G15(deposition no. KCTC 10996BP) coupled to nucleocapside 58kDa of an epidemic diarrhea virus and a gold particle is attached to a reaction position of the porcine epidemic diarrhea virus antigen on a strip and a monoclonal antibody 9D11(deposition no. KCTC 10997BP) is attached to a position different from the coupling portion of the porcine epidemic diarrhea virus antigen and the monoclonal antibody 6G15. A method for diagnosing the porcine epidemic diarrhea virus antigen comprises the steps of: (a) loading a sample onto a detection pad on a strip; (b) reacting the conjugate of the monoclonal antibody 6G15 coupled to nucleocapside 58kDa of the epidemic diarrhea virus and the gold particle with the porcine epidemic diarrhea virus antigen in the sample; and (c) reacting the porcine epidemic diarrhea virus antigen, the monoclonal antibody 9D11 and the reaction product obtained from the step(b).