JP2000509241A - グリコシラーゼによる候補座位のヌクレオチド配列の検出 - Google Patents
グリコシラーゼによる候補座位のヌクレオチド配列の検出Info
- Publication number
- JP2000509241A JP2000509241A JP9505644A JP50564497A JP2000509241A JP 2000509241 A JP2000509241 A JP 2000509241A JP 9505644 A JP9505644 A JP 9505644A JP 50564497 A JP50564497 A JP 50564497A JP 2000509241 A JP2000509241 A JP 2000509241A
- Authority
- JP
- Japan
- Prior art keywords
- dna
- nucleic acid
- glycosylase
- primer
- uracil
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING 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
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6813—Hybridisation assays
- C12Q1/6834—Enzymatic or biochemical coupling of nucleic acids to a solid phase
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING 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
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6813—Hybridisation assays
- C12Q1/6827—Hybridisation assays for detection of mutation or polymorphism
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING 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
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6844—Nucleic acid amplification reactions
- C12Q1/6853—Nucleic acid amplification reactions using modified primers or templates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING 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
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6888—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms
- C12Q1/689—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms for bacteria
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING 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
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Analytical Chemistry (AREA)
- Microbiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Physics & Mathematics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Saccharide Compounds (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1. 以下の工程を含む、標的核酸試料中の候補座位(locus)における特定 の核酸配列の有無の迅速な検出方法: i)前記候補座位の事前選択された一つまたはそれ以上の位置(position)へ DNAグリコシラーゼに対する基質である修飾塩基を導入し; ii)非塩基部位(abasic)を生じるように、前記DNAグリコシラーゼにより 修飾塩基を切除(excise)し;そして iii)工程ii)で生じた非塩基部位(abasic)のリン酸結合を切断し(cleave ); iv)前記標的核酸配列中の前記候補座位の前記特定の核酸配列の有無を同定す るために、工程iii)の切断産物を解析すること。 2. 正常なDNA前駆体ヌクレオチドおよび少なくとも一つの被修飾前駆体 ヌクレオチドを組み合わせて用いることで候補座位を増幅する、請求項1の方法 。 3. 少なくとも一つの増幅プライマーが候補座位に隣接する、請求項2の方 法。 4. 少なくとも一つのプライマーを標識する、請求項3の方法。 5. 少なくとも一つの前駆体ヌクレオチドを標識する、請求項2から4のいず れか一項の方法。 6. 化学修飾によって修飾塩基を候補座位に導入する、請求項1から5のの いずれか一項の方法。 7. DNAグリコシラーゼ酵素によって修飾塩基を切除する(excisc)、請 求項1から6のいずれか一項の方法。 8. DNAグリコシラーゼ酵素がウラシルDNAグリコシラーゼである、請 求項7の方法。 9. DNAグリコシラーゼ酵素の基質を固定化する、請求項7または8の方法 。 10.アルカリで処理することによって非塩基部位のリン酸結合を切断する、 請求項1から9のいずれか一項の方法。 11.熱処理によって非塩基部位のリン酸結合を切断する、請求項1から9のい ずれか一項の方法。 12.酵素処理によって非塩基部位のリン酸結合をが切断する、請求項1から 9のいずれか一項の方法。 13.酵素が、非プリンまたは非ピリミジン部位を特異的に切断する酵素であ る、請求項12の方法。 14.修飾塩基がウラシルまたはヒポキサンチンである、請求項1から13のい ずれか一項の方法。 15.標的核酸試料がDNAである、請求項1から14のいずれか一項の方法。 16.DNAが一本鎖、ホモ二本鎖、またはヘテロ二本鎖DNAである、請求 項15の方法。 17.標的核酸試料がRNAである、請求項1から14のいずれか一項の方法。 18.増幅工程に先だって逆転写によってRNAをcDNAに変換する、請求 項2に従属する場合の、請求項17の方法。 19.切断産物を特異的核酸プローブによるハイブリダイゼーションによって 検出する、請求項1から18のいずれか一項の方法。 20.請求項1から19のいずれか一項の方法を実施するための、試験用キット またはパック。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IE950526 | 1995-07-11 | ||
IE950526 | 1995-07-11 | ||
PCT/IE1995/000067 WO1997003210A1 (en) | 1995-07-11 | 1995-12-21 | Glycosylase mediated detection of nucleotide sequences at candidate loci |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2000509241A true JP2000509241A (ja) | 2000-07-25 |
JP3790797B2 JP3790797B2 (ja) | 2006-06-28 |
Family
ID=11040818
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP50564497A Expired - Fee Related JP3790797B2 (ja) | 1995-07-11 | 1995-12-21 | グリコシラーゼによる候補座位のヌクレオチド配列の検出 |
Country Status (13)
Country | Link |
---|---|
US (1) | US5952176A (ja) |
EP (1) | EP0843735B2 (ja) |
JP (1) | JP3790797B2 (ja) |
AT (1) | ATE220725T1 (ja) |
AU (1) | AU708821B2 (ja) |
CA (1) | CA2226542C (ja) |
DE (1) | DE69527444T3 (ja) |
DK (1) | DK0843735T4 (ja) |
ES (1) | ES2176358T3 (ja) |
NO (1) | NO980105L (ja) |
NZ (1) | NZ298494A (ja) |
PT (1) | PT843735E (ja) |
WO (1) | WO1997003210A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006504399A (ja) * | 2002-04-12 | 2006-02-09 | ニュー・イングランド・バイオラブズ・インコーポレイティッド | Dna操作のための方法および組成物 |
JP2006515987A (ja) * | 2002-11-27 | 2006-06-15 | セクエノム,インコーポレイティド | 配列変化検出及び発見用の断片化をベースとする方法及びシステム |
Families Citing this family (51)
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US6190865B1 (en) | 1995-09-27 | 2001-02-20 | Epicentre Technologies Corporation | Method for characterizing nucleic acid molecules |
SE9601676D0 (sv) | 1996-04-30 | 1996-04-30 | Ulf Landegren | Improved probing of specific mucleic acids |
US6197557B1 (en) | 1997-03-05 | 2001-03-06 | The Regents Of The University Of Michigan | Compositions and methods for analysis of nucleic acids |
US6117634A (en) * | 1997-03-05 | 2000-09-12 | The Reagents Of The University Of Michigan | Nucleic acid sequencing and mapping |
US5885958A (en) * | 1997-03-25 | 1999-03-23 | Administrators Of The Tulane Educational Fund | Mu-opiate receptor peptides |
WO1998054571A1 (en) * | 1997-05-28 | 1998-12-03 | The Walter And Eliza Hall Institute Of Medical Research | Nucleic acid diagnostics based on mass spectrometry or mass separation and base specific cleavage |
US6090553A (en) * | 1997-10-29 | 2000-07-18 | Beckman Coulter, Inc. | Use of uracil-DNA glycosylase in genetic analysis |
WO1999042622A1 (en) * | 1998-02-23 | 1999-08-26 | Dana-Farber Cancer Institute, Inc. | Method for identifying mismatch repair glycosylase reactive sites, compound and uses thereof_____________________________________ |
US7175982B1 (en) * | 1998-04-22 | 2007-02-13 | Enterprise Ireland (T/A BioResearch Ireland) | Method for the characterization of nucleic acid molecules involving generation of extendible upstream DNA fragments resulting from the cleavage of nucleic acid at an abasic site |
US6048696A (en) * | 1998-05-13 | 2000-04-11 | Epicentre Technologies Corporation | Method of identifying nucleic acid molecules |
US7270958B2 (en) | 1998-09-10 | 2007-09-18 | The Regents Of The University Of Michigan | Compositions and methods for analysis of nucleic acids |
US6440705B1 (en) * | 1998-10-01 | 2002-08-27 | Vincent P. Stanton, Jr. | Method for analyzing polynucleotides |
EP1041159A3 (de) * | 1999-03-26 | 2000-10-25 | MIRA Diagnostika GmbH | Verfahren, Oligonucleotide zum Abbau von in-vitro synthetisierten Nucleinsäuremolekülen |
US20030207295A1 (en) * | 1999-04-20 | 2003-11-06 | Kevin Gunderson | Detection of nucleic acid reactions on bead arrays |
US20060275782A1 (en) | 1999-04-20 | 2006-12-07 | Illumina, Inc. | Detection of nucleic acid reactions on bead arrays |
US20030207297A1 (en) * | 1999-10-13 | 2003-11-06 | Hubert Koster | Methods for generating databases and databases for identifying polymorphic genetic markers |
EP1261932B1 (en) | 1999-10-13 | 2009-09-30 | Sequenom, Inc. | Methods for identifying polymorphic genetic markers |
US7668658B2 (en) | 1999-10-13 | 2010-02-23 | Sequenom, Inc. | Methods for generating databases and databases for identifying polymorphic genetic markers |
CA2426824A1 (en) * | 2000-10-24 | 2002-07-25 | The Board Of Trustees Of The Leland Stanford Junior University | Direct multiplex characterization of genomic dna |
EP1332208A2 (en) * | 2000-10-30 | 2003-08-06 | Gene Logic, Inc. | Partially double-stranded nucleic acids, methods of making, and use thereof |
IE20000887A1 (en) * | 2000-11-03 | 2002-12-11 | Univ College Cork Nat Univ Ie | Method for the amplification and optional characterisation of nucleic acids |
WO2002081753A1 (en) * | 2001-04-04 | 2002-10-17 | Advanced Research & Technology Institute | Method for identifying and characterizing individual dna molecules |
US20110151438A9 (en) | 2001-11-19 | 2011-06-23 | Affymetrix, Inc. | Methods of Analysis of Methylation |
CN1697882A (zh) * | 2001-11-19 | 2005-11-16 | 帕拉里勒生物科学公司 | 多重pcr |
WO2004011665A2 (en) * | 2002-05-17 | 2004-02-05 | Nugen Technologies, Inc. | Methods for fragmentation, labeling and immobilization of nucleic acids |
IE20020544A1 (en) * | 2002-06-28 | 2003-12-31 | Univ College Cork Nat Univ Ie | Method for the characterisation of nucleic acid molecules |
CA2515583C (en) | 2003-03-07 | 2015-07-14 | Diversa Corporation | Hydrolases, nucleic acids encoding them and methods for making and using them |
US20050239087A1 (en) * | 2003-04-29 | 2005-10-27 | Haiguang Xiao | Multiply-primed amplification of nucleic acid sequences |
US20050181394A1 (en) * | 2003-06-20 | 2005-08-18 | Illumina, Inc. | Methods and compositions for whole genome amplification and genotyping |
WO2005003304A2 (en) | 2003-06-20 | 2005-01-13 | Illumina, Inc. | Methods and compositions for whole genome amplification and genotyping |
US9394565B2 (en) | 2003-09-05 | 2016-07-19 | Agena Bioscience, Inc. | Allele-specific sequence variation analysis |
WO2005065321A2 (en) | 2003-12-29 | 2005-07-21 | Nugen Technologies, Inc. | Methods for analysis of nucleic acid methylation status and methods for fragmentation, labeling and immobilization of nucleic acids |
WO2005098050A2 (en) | 2004-03-26 | 2005-10-20 | Sequenom, Inc. | Base specific cleavage of methylation-specific amplification products in combination with mass analysis |
US7608394B2 (en) | 2004-03-26 | 2009-10-27 | Sequenom, Inc. | Methods and compositions for phenotype identification based on nucleic acid methylation |
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EP2145180B1 (en) * | 2007-04-13 | 2013-12-04 | Sequenom, Inc. | Comparative sequence analysis processes and systems |
WO2009117031A2 (en) * | 2007-12-18 | 2009-09-24 | Advanced Analytical Technologies, Inc. | System and method for nucleotide sequence profiling for sample identification |
US20230148447A9 (en) | 2008-12-11 | 2023-05-11 | Pacific Biosciences Of California, Inc. | Classification of nucleic acid templates |
US9175338B2 (en) | 2008-12-11 | 2015-11-03 | Pacific Biosciences Of California, Inc. | Methods for identifying nucleic acid modifications |
US9175341B2 (en) | 2008-12-11 | 2015-11-03 | Pacific Biosciences Of California, Inc. | Methods for identifying nucleic acid modifications |
WO2011036609A1 (en) | 2009-09-23 | 2011-03-31 | Koninklijke Philips Electronics N.V. | Method for monitoring the bisulfite-mediated conversion of dna |
EP2769007B1 (en) | 2011-10-19 | 2016-12-07 | Nugen Technologies, Inc. | Compositions and methods for directional nucleic acid amplification and sequencing |
SG11201404243WA (en) | 2012-01-26 | 2014-08-28 | Nugen Technologies Inc | Compositions and methods for targeted nucleic acid sequence enrichment and high efficiency library generation |
WO2013163207A1 (en) | 2012-04-24 | 2013-10-31 | Pacific Biosciences Of California, Inc. | Identification of 5-methyl-c in nucleic acid templates |
WO2013191775A2 (en) | 2012-06-18 | 2013-12-27 | Nugen Technologies, Inc. | Compositions and methods for negative selection of non-desired nucleic acid sequences |
US20150011396A1 (en) | 2012-07-09 | 2015-01-08 | Benjamin G. Schroeder | Methods for creating directional bisulfite-converted nucleic acid libraries for next generation sequencing |
EP2971130A4 (en) | 2013-03-15 | 2016-10-05 | Nugen Technologies Inc | SEQUENTIAL SEQUENCING |
CN105849264B (zh) | 2013-11-13 | 2019-09-27 | 纽亘技术公司 | 用于鉴别重复测序读数的组合物和方法 |
WO2015131107A1 (en) | 2014-02-28 | 2015-09-03 | Nugen Technologies, Inc. | Reduced representation bisulfite sequencing with diversity adaptors |
CA2957633A1 (en) | 2014-08-06 | 2016-02-11 | Nugen Technologies, Inc. | Digital measurements from targeted sequencing |
US11099202B2 (en) | 2017-10-20 | 2021-08-24 | Tecan Genomics, Inc. | Reagent delivery system |
Family Cites Families (2)
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DE69130800T2 (de) * | 1990-07-24 | 1999-09-16 | Hoffmann La Roche | Verringerung von nicht spezifischer amplifikation während einer (in vitro) nukleinsäure amplifikation unter verwendung von modifizierten nukleinsäure basen |
US6190865B1 (en) † | 1995-09-27 | 2001-02-20 | Epicentre Technologies Corporation | Method for characterizing nucleic acid molecules |
-
1995
- 1995-12-21 AU AU43995/96A patent/AU708821B2/en not_active Ceased
- 1995-12-21 AT AT95942776T patent/ATE220725T1/de not_active IP Right Cessation
- 1995-12-21 NZ NZ298494A patent/NZ298494A/en unknown
- 1995-12-21 JP JP50564497A patent/JP3790797B2/ja not_active Expired - Fee Related
- 1995-12-21 PT PT95942776T patent/PT843735E/pt unknown
- 1995-12-21 US US08/981,663 patent/US5952176A/en not_active Expired - Fee Related
- 1995-12-21 DE DE69527444T patent/DE69527444T3/de not_active Expired - Fee Related
- 1995-12-21 EP EP95942776A patent/EP0843735B2/en not_active Expired - Lifetime
- 1995-12-21 WO PCT/IE1995/000067 patent/WO1997003210A1/en active IP Right Grant
- 1995-12-21 ES ES95942776T patent/ES2176358T3/es not_active Expired - Lifetime
- 1995-12-21 DK DK95942776T patent/DK0843735T4/da active
- 1995-12-21 CA CA002226542A patent/CA2226542C/en not_active Expired - Fee Related
-
1998
- 1998-01-09 NO NO980105A patent/NO980105L/no not_active Application Discontinuation
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006504399A (ja) * | 2002-04-12 | 2006-02-09 | ニュー・イングランド・バイオラブズ・インコーポレイティッド | Dna操作のための方法および組成物 |
JP4663988B2 (ja) * | 2002-04-12 | 2011-04-06 | ニュー・イングランド・バイオラブズ・インコーポレイティッド | Dna操作のための方法および組成物 |
JP2006515987A (ja) * | 2002-11-27 | 2006-06-15 | セクエノム,インコーポレイティド | 配列変化検出及び発見用の断片化をベースとする方法及びシステム |
JP4786904B2 (ja) * | 2002-11-27 | 2011-10-05 | セクエノム,インコーポレイティド | 配列変化検出及び発見用の断片化をベースとする方法及びシステム |
Also Published As
Publication number | Publication date |
---|---|
DE69527444T2 (de) | 2003-02-20 |
DE69527444D1 (de) | 2002-08-22 |
DE69527444T3 (de) | 2007-08-16 |
AU708821B2 (en) | 1999-08-12 |
WO1997003210A1 (en) | 1997-01-30 |
US5952176A (en) | 1999-09-14 |
ES2176358T3 (es) | 2002-12-01 |
EP0843735A1 (en) | 1998-05-27 |
NO980105L (no) | 1998-03-10 |
CA2226542C (en) | 2006-04-04 |
EP0843735B1 (en) | 2002-07-17 |
ATE220725T1 (de) | 2002-08-15 |
JP3790797B2 (ja) | 2006-06-28 |
DK0843735T4 (da) | 2007-01-22 |
EP0843735B2 (en) | 2006-12-27 |
DK0843735T3 (da) | 2002-11-11 |
CA2226542A1 (en) | 1997-01-30 |
NZ298494A (en) | 1999-09-29 |
AU4399596A (en) | 1997-02-10 |
NO980105D0 (no) | 1998-01-09 |
PT843735E (pt) | 2002-11-29 |
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