KR950032642A - Detection of Nephrotic Hemorrhagic Fever Virus - Google Patents

Detection of Nephrotic Hemorrhagic Fever Virus Download PDF

Info

Publication number
KR950032642A
KR950032642A KR1019950010997A KR19950010997A KR950032642A KR 950032642 A KR950032642 A KR 950032642A KR 1019950010997 A KR1019950010997 A KR 1019950010997A KR 19950010997 A KR19950010997 A KR 19950010997A KR 950032642 A KR950032642 A KR 950032642A
Authority
KR
South Korea
Prior art keywords
nucleic acid
seq
represented
sequence
variant sequence
Prior art date
Application number
KR1019950010997A
Other languages
Korean (ko)
Other versions
KR100386135B1 (en
Inventor
스이게토시 미즈타니
히로유키 무카이
아쯔시 오시마
기요조 아사다
가쯔토 다케사코
이쿠노신 가토
유지 이세가와
Original Assignee
오미야 히사시
다카라쯔죠 가부시끼가이샤
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 오미야 히사시, 다카라쯔죠 가부시끼가이샤 filed Critical 오미야 히사시
Publication of KR950032642A publication Critical patent/KR950032642A/en
Application granted granted Critical
Publication of KR100386135B1 publication Critical patent/KR100386135B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/70Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving virus or bacteriophage
    • C12Q1/701Specific hybridization probes
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2533/00Reactions characterised by the enzymatic reaction principle used
    • C12Q2533/10Reactions characterised by the enzymatic reaction principle used the purpose being to increase the length of an oligonucleotide strand
    • C12Q2533/101Primer extension

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Wood Science & Technology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Virology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Molecular Biology (AREA)
  • Physics & Mathematics (AREA)
  • Biophysics (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

본 발명은 서열 목록에서 SEQ ID Nos. 1 내지 5로 표시되는 핵산 및 그것의 상보 서열들로 이루어지는 군으로부터 선택된 최소한 하나의 핵산의 일부분을 역전사 및 2단계의 중합효소 연쇄 반응(PCR)에 의해 증폭시키는 것으로 이루어지는, 신증후성 출혈열 바이러스(이하 HFRSV라 언급한다)의 검출 방법, 이 방법에 의해 DNA가 증폭되는 시험될 샘플중의 HFRSV를 검출하기 위한 방법 및 특징의 핵산 서열 또는 그것의 변이 서열을 가지는, HFRSV 검출에 사용하기 위한 프라이머에 관한 것이다.The present invention relates to SEQ ID Nos. Nephrotic hemorrhagic fever virus (hereinafter referred to as amplification of a portion of at least one nucleic acid selected from the group consisting of nucleic acids represented by 1 to 5 and its complementary sequences by reverse transcription and two-step polymerase chain reaction (PCR)) A method for detecting HFRSV in a sample to be tested, wherein the DNA is amplified by the method, and a primer for use in HFRSV detection having a nucleic acid sequence or a variant sequence thereof. will be.

Description

신증후성 출혈열 바이러스의 검출방법Detection of Nephrotic Hemorrhagic Fever Virus

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음As this is a public information case, the full text was not included.

Claims (7)

서열 목록에서 SEQ ID Nos. 1 내지 5로 표시되는 핵산 및 그것의 상보 서열들로 이루어지는 군으로부터 선택된 최소한 하나의 핵산의 일부분을 역전사 및 2단계의 중합효소 연쇄 반응(PCR)에 의해 증폭시키는 것으로 이루어지는, 신증후성 출혈열 바이러스의 검출 방법.SEQ ID Nos. Detection of nephrotic hemorrhagic fever virus, comprising amplifying a portion of at least one nucleic acid selected from the group consisting of the nucleic acids represented by 1 to 5 and its complementary sequences by reverse transcription and a two-step polymerase chain reaction (PCR) Way. (a)시험할 샘플로부터 핵산을 단리하는 단계; (b)단리된 핵산에 대해, 서열 목록의 SEQ ID No.6으로 표시되는 핵산 단편 구설의 변이 서열 및 또는 목록의 SEQ ID No. 7로 표시되는 핵산 단편 또는 그것의 변이 서열로 이루어지는 군으로부터 선택되는 프라이머를 사용하여 역전사를 수행함으로써 역전사 DNA 생성물을 얻는 단계; (c)역전사 DNA생성물에 대해, 서열 목록의 SEQ ID No. 6으로 표시되는 핵산 단편 또는 그것의 변이 서열을 서열 목록의 SEQ ID No. 7로 표시되는 핵산 단편 또는 그것의 변이 서열과 조합하여 사용하는 첫번째 PCR 단계를 수행함으로써 DNA를 증폭시키는 단계; (d)증폭된 DNA에 대해, 서열 목록의 SEQ ID No. 8로 표시되는 핵산 단편 또는 그것의 변이 서열을 서열 목록의 SEQ ID No. 9로 표시되는 핵산 단편 또는 그것의 변이 서열과 조합하여 사용하는 두번째 PCR단계를 수행함으로써 DNA를 증폭시키는 단계; 그리고 (e)증폭된 DNA를 검출하는 단계로 이루어지는, 시험할 샘플중에 함유된 신증후성 출혈열 바이러스의 검출 방법.(a) isolating nucleic acid from the sample to be tested; (b) for an isolated nucleic acid, the mutant sequence of the nucleic acid fragment construct represented by SEQ ID No. 6 in the Sequence Listing and / or SEQ ID No. Obtaining reverse transcription DNA product by performing reverse transcription using a primer selected from the group consisting of the nucleic acid fragment represented by 7 or a variant sequence thereof; (c) For reverse transcription DNA products, SEQ ID No. The nucleic acid fragment represented by 6 or a variant sequence thereof is selected from SEQ ID No. Amplifying the DNA by performing the first PCR step used in combination with the nucleic acid fragment represented by 7 or a variant sequence thereof; (d) for amplified DNA, SEQ ID No. The nucleic acid fragment represented by 8 or a variant sequence thereof is selected from SEQ ID No. Amplifying the DNA by performing a second PCR step used in combination with the nucleic acid fragment represented by 9 or a variant sequence thereof; And (e) detecting the amplified DNA. 서열 목록에서 SEQ ID No. 6,7,8 또는 9로 표시되는 핵산 또는 그것의 변이 서열을 가지는, 신증후성 출혈열 바이러스의 검출에 사용하기 위한 프라이머.SEQ ID No. in the sequence listing. A primer for use in the detection of nephrotic hemorrhagic fever virus having a nucleic acid represented by 6,7,8 or 9 or a variant sequence thereof. 제3항에 있어서, SEQ ID No. 6,7,8 및 9의 변이 서열이 각각 SEQ ID No. 27,28,29 및 30으로 표시되는 핵산 서열인 것을 특징으로 하는 프라이머.The method of claim 3, wherein SEQ ID No. The variant sequences of 6,7,8 and 9 are shown by SEQ ID No. A primer characterized in that the nucleic acid sequence represented by 27,28,29 and 30. SEQ ID No. 6으로 표시되는 핵산 서열 또는 그것의 변이 서열 및 SEQ ID No. 7로 표시되는 핵산 서열 또는 그것의 변이 서열을 가지는 프라이머 쌍과 SEQ ID No. 8로 표시되는 핵산 서열 또는 그것의 변이 서열 및 SEQ ID No. 9로 표시되는 핵산 서열 또는 그것의 변이 서열을 가지는 다른 프라이머 쌍을 포함하는, 신증후성 출혈열 바이러스를 검출하기 위한 키트.SEQ ID No. The nucleic acid sequence represented by 6 or a variant sequence thereof and SEQ ID No. A primer pair having a nucleic acid sequence represented by 7 or a variant sequence thereof and SEQ ID No. The nucleic acid sequence represented by 8 or its variant sequence and SEQ ID No. A kit for detecting nephrotic hemorrhagic fever virus, comprising another primer pair having a nucleic acid sequence represented by 9 or a variant sequence thereof. 제5항에 있어서, 혈액으로부터 RNA를 단리하기 위한 시약, 역전사효소 및 PCR 시약들을 추가로 포함하는 것을 특징으로 하는 키트.6. The kit of claim 5 further comprising reagents, reverse transcriptases and PCR reagents for isolating RNA from blood. 제5항에 있어서, 역전사효소, DNA 중합효소, RNAse 억제제, 완충제, 염화 마그네슘, dNTP 혼합물 및 양성 대조표준 RNA를 추가로 포함하는 것을 특징으로 하는 키트.6. The kit of claim 5 further comprising reverse transcriptase, DNA polymerase, RNAse inhibitor, buffer, magnesium chloride, dNTP mixture and positive control RNA. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019950010997A 1994-05-06 1995-05-04 Detection of Nephrotic Hemorrhagic Fever Virus KR100386135B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP1994-116037 1994-05-06
JP11603794 1994-05-06

Publications (2)

Publication Number Publication Date
KR950032642A true KR950032642A (en) 1995-12-22
KR100386135B1 KR100386135B1 (en) 2004-09-07

Family

ID=14677175

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019950010997A KR100386135B1 (en) 1994-05-06 1995-05-04 Detection of Nephrotic Hemorrhagic Fever Virus

Country Status (2)

Country Link
KR (1) KR100386135B1 (en)
CN (1) CN1066199C (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101294226B (en) * 2008-04-17 2010-09-01 武汉大学 RT-PCR method for testing hantavirus genome

Also Published As

Publication number Publication date
KR100386135B1 (en) 2004-09-07
CN1122835A (en) 1996-05-22
CN1066199C (en) 2001-05-23

Similar Documents

Publication Publication Date Title
US5849547A (en) Method for nucleic acid amplification by transcription using displacement, and reagents and kit therefor
Nie et al. Detection of multiple potato viruses using an oligo (dT) as a common cDNA primer in multiplex RT-PCR
JP3140937B2 (en) Strand displacement amplification using a thermophilic enzyme
Karami et al. A review of the current isothermal amplification techniques: applications, advantages and disadvantages
KR950704508A (en) METHODS FOR SEQUENCING SYNTHETIC OLIGONUCLEOTIDES CONTAINING NON-PHOSPHODIESTER INTERNUCLEOTIDE LINKAGES
WO2001090417A3 (en) Materials and methods for detection of nucleic acids
KR870007427A (en) How to detect viruses by amplification and hybridization
KR920014937A (en) Amplification method by chain substitution
JP2006020642A (en) Oligonucleotide primers for amplifying hcv nucleic acid
WO2004059289A3 (en) Target-dependent transcription using deletion mutants of n4 rna polymerase
JP2011505129A (en) Nucleic acid detection method using simultaneous isothermal amplification of nucleic acid and signal probe
JP2008526231A (en) Identification of RNA targets using helicases
DE60020143D1 (en) TYPISING HUMAN ENTEROVIRES
GB2485275A (en) Strand displacement activity of modified polymerases
JPH11506013A (en) Methods and kits for determining the pre-amplification level of a nucleic acid target sequence from the post-amplification level of a product
KR20120018734A (en) Kit for detecting hepatitis b virus and method for detecting hepatitis b virus using the same
KR20120020067A (en) Kit for detecting hepatitis c virus and method for detecting hepatitis c virus using the same
JP2008136451A (en) Method for amplifying nucleic acid
KR20100090730A (en) Nucleic acid detection
KR930008138A (en) Attenuated Measles Vaccine Virus Strains Containing Specific Nucleotide Sequences and Their Complete Identification Methods
EP4118205A1 (en) Looped primer and loop-de-loop method for detecting target nucleic acid
JPWO2005001097A1 (en) Detection method of SARS coronavirus
JP2006508656A (en) Method for reducing both the effects of sequence variation and the effect of baseline rise in diagnostic hybridization assays, assays for carrying out such methods and probes for use in said assays
DE60229025D1 (en) Detection of nucleic acid deletion sequences
JP2016019495A (en) Nucleic acid amplification technique

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20070511

Year of fee payment: 5

LAPS Lapse due to unpaid annual fee