Abstract:
PURPOSE: A PCR primer pair for detecting Xanthomonas campestris pv. inc is provided to ensure specific sequence to Xanthomonas campestris pv. inc-specific gene. CONSTITUTION: A PCR primer pair for detecting Xanthomonas campestris pv. inc is denoted by sequence numbers 1 and 2 or 3 and 4. A composition for detecting Xanthomonas campestris pv. inc contains the primer pair. A kit for detecting Xanthomonas campestris pv. inc contains the primer pair. A method for detecting Xanthomonas campestris pv. inc comprises: a step of isolating DNA from a sample; a step of amplifying the DNA by PCR using the primer pair; and a step of detecting the PCR product by electrophoresis.
Abstract:
PURPOSE: Specific primers for detecting zucchini yellow mosaic virus are provided, thereby increasing the detection limitation and sensitivity about 1,000 times higher than using antiserum, detecting all kinds of zucchini yellow mosaic virus, and improving the detection accuracy by removing nonspecific reaction with other related viruses. CONSTITUTION: The specific primers for detecting zucchini yellow mosaic virus comprise a nucleic acid fragment selected from the nucleotide sequence set forth in SEQ ID NO: 2, SEQ ID NO: 4 or SEQ ID NO: 5 which species specifically binds with zucchini yellow mosaic virus, complementary nucleotide sequences thereof, and mutated nucleotide sequences thereof; and another nucleic acid fragment selected from the nucleotide sequence set forth in SEQ ID NO: 7 or SEQ ID NO: 8 which is combined with the selected nucleic acid and species specifically binds with zucchini yellow mosaic virus, complementary nucleotide sequences thereof, and mutated nucleotide sequences thereof, wherein the mutation is selected from deletion of base, addition of base, substitution of base or the combination thereof.
Abstract translation:目的:提供用于检测西葫芦黄花叶病毒的特异性引物,从而提高检测限度和灵敏度,比使用抗血清高约1000倍,检测各种西葫芦黄花叶病毒,并通过去除与其他相关病毒的非特异性反应来提高检测精度 。 构成:用于检测西葫芦黄花叶病毒的特异性引物包含选自SEQ ID NO:2,SEQ ID NO:4或SEQ ID NO:5所示核苷酸序列的核酸片段,该核苷酸序列特异性结合西葫芦黄花叶病毒 ,其互补核苷酸序列及其突变核苷酸序列; 和选自SEQ ID NO:7或SEQ ID NO:8所示核苷酸序列的另一核酸片段,其与选择的核酸和物种组合特异性结合西葫芦黄花叶病毒,其互补核苷酸序列和突变核苷酸 序列,其中突变选自碱基的缺失,碱的加入,碱的取代或其组合。
Abstract:
PURPOSE: A PCR primer pair for detecting Xanthomonas campestris pv. sesame is provided to diagnose and detect Xanthomonas campestris pv. sesame. CONSTITUTION: A primer pair for detecting Xanthomonas campestris pv. sesame is denoted by sequence numbers 1 and 2 or 3 and 4. A composition for detecting Xanthomonas campestris pv. sesame contains the primer pair. A kit for detecting Xanthomonas campestris pv. sesame contains the pair.
Abstract:
본 발명은 쥬키니황화모자이크바이러스와 종 특이적으로 반응하는 핵산단편에 관한 것으로, 보다 상세하게는 서열번호 2,4,5,7,8로 표시되는 염기서열, 그의 상보적인 염기서열 또는 이들 염기서열에 의거한 변이가 실시된 변형서열의 어느 하나의 핵산단편 또는 이들 핵산 단편의 특정 조합으로 구성되는 프라이머를 개시한다. 본 발명에 의하면 항혈청을 이용한 진단방법보다 1,000배 이상 검출한계가 높으며, 지금까지 알려진 쥬키니항화모자이크바이러스의 모든 계통에 대한 검출이 가능하다. 또한 다른 관련 바이러스와의 비특이적 반응이 없어 훨씬 정밀하게 쥬키니황화모자이크바이러스의 감염여부를 진단할 수 있다.
Abstract:
PURPOSE: Specific primers for detecting pepper mild mottle virus are provided, thereby increasing the detection limitation and sensitivity about 1,000 times higher than using antiserum, detecting all kinds of pepper mild mottle virus, and improving the detection accuracy by removing nonspecific reaction with other related viruses. CONSTITUTION: The specific primers for detecting pepper mild mottle virus comprise a nucleic acid fragment selected from the nucleotide sequence set forth in SEQ ID NO: 1 or SEQ ID NO: 4 which species specifically binds with pepper mild mottle virus, complementary nucleotide sequences thereof, and mutated nucleotide sequences thereof; and another nucleic acid fragment selected from the nucleotide sequence set forth in SEQ ID NO: 5 or SEQ ID NO: 6 which is combined with the selected nucleic acid and species specifically binds with pepper mild mottle virus, complementary nucleotide sequences thereof, and mutated nucleotide sequences thereof, wherein the mutation is selected from deletion of base, addition of base, substitution of base or the combination thereof.
Abstract translation:目的:提供用于检测辣椒轻度斑驳病毒的特异性引物,从而提高检测限度和灵敏度,比使用抗血清高约1000倍,检测各种胡椒柔和斑驳病毒,并通过去除与其他相关病毒的非特异性反应来提高检测准确度 。 构成:用于检测辣椒柔和斑驳病毒的特异性引物包含选自SEQ ID NO:1或SEQ ID NO:4所示核苷酸序列的核酸片段,该核苷酸序列与辣椒柔和斑驳病毒特异性结合,其互补核苷酸序列, 及其突变核苷酸序列; 和选自与选择的核酸和物种组合的SEQ ID NO:5或SEQ ID NO:6所示核苷酸序列的另一个核酸片段与辣椒柔和斑驳病毒,其互补核苷酸序列和突变核苷酸特异性结合 序列,其中突变选自碱基的缺失,碱的加入,碱的取代或其组合。
pv . sesami ) 검출용 PCR 프라이머 쌍에 관한 것으로 보다 상세하게는 서열번호 1 및 서열번호 2 또는 서열번호 3 및 서열번호 4로 표시되는 PCR 프라이머 쌍, 상기 프라이머 쌍을 포함하는 참깨 세균잎마름병균 검출용 조성물 및 검출용 키트 및 상기 프라이머 쌍을 이용한 참깨 세균잎마름병균 미생물의 검출 방법에 관한 것이다. 본 발명의 프라이머 쌍은 참깨 세균잎마름병균에 특이적인 유전자에 특이적인 서열을 가지므로, 참깨 세균잎마름병균의 진단 및 검출에 사용될 수 있다.
Abstract:
PURPOSE: A PCR primer pair having a sequence which is specific to a specific gene in entire Xanthomonas sp. is provided to detect microorganism belonging to Xanthomonas sp. CONSTITUTION: A PCR primer pair for detecting Xanthomonas sp. microbes is denoted by sequence numbers 1 and 2. The primer pair is denoted by sequence numbers 3 and 4. A composition for detecting Xanthomonas sp. microbes contains the primer pair. A method for detecting Xanthomonas sp. comprises: a step of isolating DNA from a sample; a step of amplifying the DNA using the primer pair; and a step of detecting PCR product by electrophoresis.
Abstract:
PURPOSE: A Pectobacterium carotovorum Pcc21-M15 producing bacteriocin carocin D is provided to prevent bacterial soft rot and use microorganism agricultural chemical. CONSTITUTION: A Pectobacterium carotovorum Pcc21-M15(KACC91406) has bacteriocin activity. A gene encoding protein of sequence number 2 having bacteriocin activity has sequence of sequence number 1. A formulation for preventing bacterial soft rot contains Pectobacterium carotovorum Pcc21-M15 as an active ingredient. The formulation for preventing bacterial soft rot contains the protein having bacteriocin activity as an active ingredient. The formulation for preventing bacterial soft rot contains transformant transformed with the gene encoding the protein.
Abstract:
PURPOSE: A PCR primer pair for detecting Xanthomonas populi is provided to diagnose and detect Xanthomonas populi. CONSTITUTION: A PCR primer pair for detecting Xanthomonas populi is denoted by sequence numbers 1 and 2 or 3 and 4. A kit for detecting Xanthomonas populi contains the primer pair. A method for detecting Xanthomonas populi comprises: a step of isolating DNA from a sample; a step of amplifying the DNA by PCR using the primer pair; and a step of detecting PCR products by electrophoresis.