Abstract:
PURPOSE: A primer set for diagnosing MNSV from melon and watermelon and a kit are provided to definitely diagnose MNSV developed in melon and watermealon. CONSTITUTION: A primer set for diagnosing MNSV from melon and watermelon is denoted by sequence numbers 1 and 2. A primer set for simultaneously diagnosing MNSV from melon and watermelon has a primer set of sequence numbers 1 and 2 and sequence number 3 and 4. The primer set has a primer set of sequence numbers 1 and 2 and sequence number 5 and 6. A kit for diagnosing MNSV from melon and watermelon contains the primer set.
Abstract:
PURPOSE: A duplex primer for diagnosing INSV and TSWV is provided to specifically diagnose INSV and TSWV and to enhance detection limit. CONSTITUTION: A duplex primer for diagnosing INSV(impatiens necrotic spot virus) and TSWV(tomato spotted wilt virus) contains oligonucleotide primer set containing an oligonucleotide with 15 or more continuous nucleotide fragment in sequence number 1 and 15 or more continuous nucleotide fragment in sequence number 2. A kit for simultaneously diagnosing INSV and TSWV contains the primer set and reagent for reverse-transcription and amplification.
Abstract:
본 발명은 멜론괴저반점바이러스(MNSV)의 멜론 분리주 및 수박 분리주의 동시진단 프라이머 세트, 이를 포함하는 진단 키트 및 이를 이용한 진단방법에 관한 것이다. 보다 자세하게는 서열번호 1 및 2로 표시되는 멜론괴저반점바이러스(MNSV)의 멜론 분리주 및 수박 분리주의 동시진단 프라이머 세트를 통하여 멜론 분리주 및 수박 분리주를 명확하게 구분하여 진단할 수 있다.
Abstract:
PURPOSE: A primer for detecting orchid virus and a detection method using the same are provided to simply detect infection by ORSV, CyMV, and OFV. CONSTITUTION: A primer set for detecting orchid virus contains: ORSV-420F primer of sequence number 1; ORSV-420R primer of sequence number 2; CyMV-620F primer of sequence number 3; CyMV-620R primer of sequence number 4, OFV-873F primer of sequence number 5; or OFV-873R primer of sequence number 6. A method for detecting orchid virus comprises: a step of performing RT-PCR and PCR using the primer and RNA isolated from a sample; and a step of determining the detection by the virus through the size of PCR products.
Abstract:
토마토에 발생하는 TYLCV를 특이적으로 진단할 수 있는 프라이머 1종 세트와 PCR의 정상 작동 유무를 판단할 수 있는 토마토 베타튜불린 (β-tubulin) 유전자 프라이머 1종 세트를 개발하여 토마토의 핵산 분리 없이 토마토 즙액을 가지고 바로 TYLCV의 진단을 정확하게 가능하도록 하고자 서열목록 1 내지 2의 PCR 프라이머 세트 및 서열번호 3 내지 4의 PCR 프라이머 세트로 구성된 토마토황화잎말림 바이러스 진단을 위한 단일 튜브-멀티플렉스 PCR 프라이머 세트를 제공한다.
Abstract:
PURPOSE: A manufacturing method of transformed potato plant with multifariousness virus resistance and a transformed potato plant manufactured by using the same are provided to increase potato productivity and to be used as a virus resistance parent. CONSTITUTION: A transformed potato plant is obtained by being transformed into an expression vector pK7GWIWG 2 which includes a gene fusing more than 3 kinds of virus genes selected from potato mop-top virus gene of the sequence number 5, PVY(Potato virus Y) gene of the sequence number 1(SEQ ID NO:1), PLRV(Potato leafroll virus) gene of the sequence number 2,PVA(Potato virus A) gene of the sequence number 3, or TRV(Tobacco rattle virus) gene of the sequence number 4 in sense and anti-sense direction. A manufacturing method of the multifariousness virus resistant transformed potato plant comprises the following steps: transforming Agrobacterium tumefaciens into an expression vector pK7GWIWG 2(I)/ YLRATRPM including YLRATRPM gene of the sequence number 6; and transforming potato cells by cocltivating agrobacterium and potato cells.
Abstract:
PURPOSE: A primer for detecting orchid virus and a detection method using the same are provided to simply detect infection by ORSV, CyMV, and OFV. CONSTITUTION: A primer set for detecting orchid virus contains: ORSV-420F primer of sequence number 1; ORSV-420R primer of sequence number 2; CyMV-620F primer of sequence number 3; CyMV-620R primer of sequence number 4, OFV-873F primer of sequence number 5; or OFV-873R primer of sequence number 6. A method for detecting orchid virus comprises: a step of performing RT-PCR and PCR using the primer and RNA isolated from a sample; and a step of determining the detection by the virus through the size of PCR products.