Abstract:
PURPOSE: A probe set for diagnosing or detecting CPMMV(cowpea mild mottle virus) is provided to minimize damage due to viral diseases in crops and to enhance production. CONSTITUTION: An oilgonucleotide probe set for diagnosing or detecting CPMMV contains one or more oligonucleotides selected from the group consisting of oligonucleotides in sequence numbers 578-587 and complementary oligonucleotides thereof. A method for diagnosing or detecting CPMMV comprises: a step of isolating RNA from a sample; a step of synthesizing cDNA using the RNA as a template; a step of hybridizing the cDNA with the probe set; and a step of identifying the hybridization. [Reference numerals] (AA) Green pea; (BB) Host: Green pea
Abstract:
PURPOSE: A probe set for diagnosing or detecting PSV(peanut stunt virus) is provided to minimize damage due to viral diseases in crops and to enhance production. CONSTITUTION: An oligonucleotide probe set for diagnosing or detecting PSV contains one or more oligonucleotides selected from the group consisting of oligonucleotides in sequence numbers 1025-1034, 1045-1049, and 2988, and complementary oligonucleotides thereof. A method for diagnosing or detecting PSV comprises: a step of isolating RNA from a sample; a step of synthesizing cDNA; a step of hybridizing the cDNA with the probe set; and a step of detecting hybridization of the cDNA and the probe set. [Reference numerals] (AA) Cowpea; (BB) Host: cowpea; (CC) Kidney bean; (DD) Host: Kidney bean
Abstract:
PURPOSE: A probe set for diagnosing or detecting BBWV2(Broad bean wilt virus2) is provided to minimize damage due to viral diseases in crops and to increase product yield. CONSTITUTION: An oligonucleotide probe set for diagnosing or detecting BBWV2 contains one or more oligonucleotides selected from the group consisting of oligonucleotides in sequence numbers 1143-1152 and 1158-1164 and complementary oligonucleotides thereof. A method for diagnosing or detecting BBWV2 comprises: a step of isolating RNA from a sample; a step of synthesizing cDNA using RNA as a template; a step of hybridizing the probe set with cDNA; and a step of detecting hybridization.
Abstract:
PURPOSE: A probe set for diagnosing Genus Carmovirus is provided to minimize viral diseases in crops and to enhance product yields. CONSTITUTION: An oligonucleotide probe set for diagnosing or detecting Genus Carmovirus contains one or more oligonucleotides selected from a group consisting of oligonucleotides of sequence numbers 674, 682-685, 691-692, 730-734, 746-748, 1452-1458, 1665-1672, 2371, and 2745-2754, and complementary oligonucleotides thereof. A method for diagnosing or detecting Genus Carmovirus comprises: a step of isolating RNA from a sample which is suspected to have Genus Carmovirus infection; a step of synthesizing cDNA; a step of hybridizing the cDNA and the probe set; and a step of detecting hybridization. [Reference numerals] (AA) Jangyeobkong; (BB) Host: Jangyeobkong
Abstract:
PURPOSE: A BrCYS7 promoter which is specific to receptable is provided to specifically induce gene expression in a certain tissue, and to effectively produce a gene product. CONSTITUTION: A promoter contains a nucleic acid sequence in sequence number 1. The promoter contains a nucleic acid sequence having 70% or more of sequence homology with the nucleic acid in sequence number 1. An expression vector contains the promoter, and is a pPBrCYS7 vector. A cell is transformed with the expression vector, and is an Agrobacterium sp. microorganism or a plant cell.
Abstract:
PURPOSE: A pollen-specific expression promoter is provided to reduce time and labor for inducing male sterility and to produce superior seeds. CONSTITUTION: A pollen-specific expression promoter PBrRF1 comprises a sequence of sequence number 1. A primer for amplifying the pollen-specific expression promoter PBrRF1 comprises oligonucleotides of sequence number 2 and sequence number 3. An expression vector pBGWFS7-PBrRF1 contains a promoter of sequence number 1. A method for preparing the expression vector pBGWFS7-PBrRF1 comprises: a step of isolating a promoter site of sequence number 1 from a Brassica campestris ssp. Pekinensis; a step of preparing a primer set of sequence numbers 2 and 3 from a genomic DNA isolated from the Arabidopsis thaliana; a step of isolating the promoter site through DNA amplification; a step of performing recombination of Pdonr221 vector and amplified PCR product to obtain a cloning vector of pDONR-PBrRF1 and pDONR-P35S; a step of performing LR recombination of pBGWFS7 vector containing a reporter system; and a step of transforming a plant body with the expression vector pBGWFS7-PBrRF1.
Abstract:
본 발명은 벼잎줄무늬병원균 또는 벼흰잎마름병원균 검출용 프라이머 쌍 및 이를 이용한 멀티플렉스 PCR 방법에 관한 것으로, 본 발명의 프라이머 쌍은 벼잎줄무늬병원균 또는 벼흰잎마름병원균의 특이 서열과 관련되어, 신속, 정확하게 벼잎줄무늬병원균 또는 벼흰잎마름병원균을 검출하는데 유용하게 이용될 수 있으며, 또한 이를 이용한 멀티플렉스 PCR 방법은 식물체가 벼잎줄무늬병원균 및 벼흰잎마름병원균에 감염 되었는지 여부를 동시에 판별하는데 유용하게 이용될 수 있다. 벼잎줄무늬병원균, 벼흰잎마름병원균, 프라이머, 멀티플렉스
Abstract:
A single expression genetic marker that is expressed according to the chromosomes of Brassica rapa genome is provided to discriminate chromosomes of Brassica rapa and quantitatively analyze the genetically modified crops of Brassica rapa. The single expression genetic marker that is expressed according to the chromosomes of Brassica rapa genome comprises 64 kinds of single expression genes located according to the related groups of Brassica rapa, having the nucleotide sequences of SEQ ID NO:1 to SEQ ID NO:64, wherein the single expression genetic marker comprises combinations of at least two genes selected from the 64 kinds of single expression genes of SEQ ID NO:1 to SEQ ID NO:64; and the single expression genes are identified by analyzing the distribution positions of single expression genes in the chromosomes of Brassica rapa.
Abstract translation:提供根据芸苔属芸苔基因组染色体表达的单一表达遗传标记,以区分芸苔属的染色体,并定量分析芸苔属的转基因作物。 根据芸苔属芸苔基因组染色体表达的单表达遗传标记包含根据芸苔属相关组的64种单一表达基因,其具有SEQ ID NO:1至SEQ ID NO:64的核苷酸序列, 其中所述单一表达遗传标记包含选自SEQ ID NO:1至SEQ ID NO:64的64种单一表达基因的至少两种基因的组合; 并通过分析芸苔属染色体中单个表达基因的分布位置来鉴定单一表达基因。