BRPI0415435A - método e kit para amplificação baseada em iniciador de ácidos nucleicos - Google Patents
método e kit para amplificação baseada em iniciador de ácidos nucleicosInfo
- Publication number
- BRPI0415435A BRPI0415435A BRPI0415435-5A BRPI0415435A BRPI0415435A BR PI0415435 A BRPI0415435 A BR PI0415435A BR PI0415435 A BRPI0415435 A BR PI0415435A BR PI0415435 A BRPI0415435 A BR PI0415435A
- Authority
- BR
- Brazil
- Prior art keywords
- amplification
- nucleic acid
- target
- tempcr
- pathogens
- Prior art date
Links
- 230000003321 amplification Effects 0.000 title abstract 8
- 238000000034 method Methods 0.000 title abstract 8
- 238000003199 nucleic acid amplification method Methods 0.000 title abstract 8
- 150000007523 nucleic acids Chemical class 0.000 title abstract 4
- 108020004707 nucleic acids Proteins 0.000 title abstract 3
- 102000039446 nucleic acids Human genes 0.000 title abstract 3
- 244000052769 pathogen Species 0.000 abstract 6
- 230000001717 pathogenic effect Effects 0.000 abstract 2
- 108091028043 Nucleic acid sequence Proteins 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000001514 detection method Methods 0.000 abstract 1
- 238000003745 diagnosis Methods 0.000 abstract 1
- 238000003748 differential diagnosis Methods 0.000 abstract 1
- 239000003999 initiator Substances 0.000 abstract 1
- 238000002955 isolation Methods 0.000 abstract 1
- 238000005457 optimization Methods 0.000 abstract 1
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
- C12Q1/6844—Nucleic acid amplification reactions
- C12Q1/686—Polymerase chain reaction [PCR]
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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
- C12Q2525/00—Reactions involving modified oligonucleotides, nucleic acids, or nucleotides
- C12Q2525/10—Modifications characterised by
- C12Q2525/155—Modifications characterised by incorporating/generating a new priming site
-
- 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
- C12Q2527/00—Reactions demanding special reaction conditions
- C12Q2527/143—Concentration of primer or probe
-
- 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
- C12Q2531/00—Reactions of nucleic acids characterised by
- C12Q2531/10—Reactions of nucleic acids characterised by the purpose being amplify/increase the copy number of target nucleic acid
- C12Q2531/113—PCR
-
- 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
- C12Q2537/00—Reactions characterised by the reaction format or use of a specific feature
- C12Q2537/10—Reactions characterised by the reaction format or use of a specific feature the purpose or use of
- C12Q2537/143—Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis
-
- 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
- C12Q2549/00—Reactions characterised by the features used to influence the efficiency or specificity
- C12Q2549/10—Reactions characterised by the features used to influence the efficiency or specificity the purpose being that of reducing false positive or false negative signals
- C12Q2549/119—Reactions characterised by the features used to influence the efficiency or specificity the purpose being that of reducing false positive or false negative signals using nested primers
-
- 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
- C12Q2565/00—Nucleic acid analysis characterised by mode or means of detection
- C12Q2565/10—Detection mode being characterised by the assay principle
- C12Q2565/102—Multiple non-interacting labels
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biophysics (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Analytical Chemistry (AREA)
- Physics & Mathematics (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
"MéTODO E KIT PARA AMPLIFICAçãO BASEADA EM INICIADOR DE áCIDOS NUCLEICOS". Um novo método para diagnóstico ou diagnóstico diferencial de agentes patogênicos e agentes patogênicos secundários é divulgado. O método divulgado utiliza um nova estratégia de amplificação denominada TemPCR para permitir amplificação sensível e específica de seqüências alvo de quaisquer agentes patogênicos e/ou agentes patogênicos secundários cuja seqüência de ácido nucleico seja conhecida. o método TemPCR utiliza pelo menos um grupo de iniciadores de enriquecimento de alvo específicos para o agente patogênico ou para o agente patogênico secundário a ser detectado (presente em uma baixa concentração) e pelo menos um par de iniciadores de amplificação de alvo compartilhado (presentes em altas concentrações) . Pelo menos um par dos citados iniciadores de enriquecimento de alvo compreende uma seqüência de ligação para os iniciadores de amplificação de alvo. Portanto, a utilização do método TemPCR permite a execução de reações de amplificação múltiplas sem a necessidade de otimização empírica dos parâmetros de amplificação múltipla. Métodos para o isolamento de ácido nucleico e para a detecção das seqüências alvo também são divulgadas para utilização com o método TemPCR.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US51076203P | 2003-10-13 | 2003-10-13 | |
PCT/US2004/033818 WO2005038039A2 (en) | 2003-10-13 | 2004-10-13 | Method for multiplex primer based amplification of nucleic acids |
Publications (1)
Publication Number | Publication Date |
---|---|
BRPI0415435A true BRPI0415435A (pt) | 2006-12-05 |
Family
ID=34465146
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BRPI0415435-5A BRPI0415435A (pt) | 2003-10-13 | 2004-10-13 | método e kit para amplificação baseada em iniciador de ácidos nucleicos |
Country Status (10)
Country | Link |
---|---|
US (1) | US7851148B2 (pt) |
EP (1) | EP1687437A4 (pt) |
JP (1) | JP4999460B2 (pt) |
KR (1) | KR100830623B1 (pt) |
CN (1) | CN1898395B (pt) |
AU (1) | AU2004282555B2 (pt) |
BR (1) | BRPI0415435A (pt) |
CA (1) | CA2542787C (pt) |
NZ (1) | NZ546903A (pt) |
WO (1) | WO2005038039A2 (pt) |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2006121773A2 (en) | 2005-05-06 | 2006-11-16 | Gen-Probe Incorporated | Compositions and assays to detect influenza virus a and b nucleic acids |
CN101248191A (zh) * | 2005-07-06 | 2008-08-20 | 生物芯片创新控股有限公司 | 分析靶核酸序列的方法与试剂盒 |
US20080053911A1 (en) * | 2006-08-30 | 2008-03-06 | Qiagen Gmbh | Separation of an organic phase from a mixture comprising organic and aqueous phases by solid phase systems |
EP2121956B1 (en) | 2006-12-21 | 2016-08-17 | Gen-Probe Incorporated | Methods and compositions for nucleic acid amplification |
GB0703996D0 (en) * | 2007-03-01 | 2007-04-11 | Oxitec Ltd | Nucleic acid detection |
US20100216138A1 (en) * | 2007-06-01 | 2010-08-26 | Alexander Alan Morley | Method for dna breakpoint analysis |
WO2009052547A1 (en) * | 2007-10-22 | 2009-04-30 | Monoquant Pty Ltd | A method of dna amplification |
BRPI0911082A2 (pt) * | 2008-04-03 | 2015-08-04 | Hudson Alpha Inst For Biotechnology | Reação de cadeia de polimerase multiplex de resgate de amplicon para amplificações de alvos múltiplos |
US9012148B2 (en) * | 2008-04-16 | 2015-04-21 | Jian Han | Method for evaluating and comparing immunorepertoires |
CN102203287B (zh) * | 2008-08-26 | 2017-09-19 | 弗卢迪格姆公司 | 增加样本和/或靶通量的测定方法 |
US8691509B2 (en) | 2009-04-02 | 2014-04-08 | Fluidigm Corporation | Multi-primer amplification method for barcoding of target nucleic acids |
US8512955B2 (en) | 2009-07-01 | 2013-08-20 | Gen-Probe Incorporated | Methods and compositions for nucleic acid amplification |
US9416419B2 (en) | 2009-11-16 | 2016-08-16 | Michael E. Hogan | Methods for PCR and HLA typing using unpurified samples |
US8771951B2 (en) * | 2009-11-16 | 2014-07-08 | Genomics Usa, Inc. | Methods for PCR and HLA typing using raw blood |
KR101287431B1 (ko) * | 2010-05-07 | 2013-07-19 | (주)진매트릭스 | 표적 유전자의 다양한 변이가 존재하는 유전자 영역을 증폭하기 위한 프라이머 조성물, 이를 이용한 표적 유전자 증폭 방법 및 이를 포함하는 pcr 증폭 키트 그리고 이를 이용한 표적 유전자의 유전자형 분석방법 |
JP2013528049A (ja) * | 2010-05-19 | 2013-07-08 | キアゲン ガイサーズバーグ アイエヌシー. | 核酸の配列特異的な精製及び多重分析のための方法及び組成物 |
CN102286612B (zh) * | 2010-06-18 | 2014-10-22 | 中国科学院上海生命科学研究院 | 一种致病微生物快速检测试剂盒 |
SG10201605049QA (en) | 2011-05-20 | 2016-07-28 | Fluidigm Corp | Nucleic acid encoding reactions |
CN104024433B (zh) * | 2011-10-31 | 2016-11-16 | 爱科来株式会社 | 基因丰度的测定方法 |
US9115394B2 (en) | 2011-12-22 | 2015-08-25 | Roche Molecular Systems, Inc. | Methods and reagents for reducing non-specific amplification |
US20150045258A1 (en) * | 2012-02-14 | 2015-02-12 | Gnubio, Inc. | Cascaded addition of target specific universal adapters to nucleic acids |
JP2015519900A (ja) | 2012-05-21 | 2015-07-16 | フリューダイム・コーポレイション | 粒子集団の単粒子解析方法及び単粒子単離方法 |
JP6464086B2 (ja) | 2012-08-30 | 2019-02-06 | ジェン−プローブ・インコーポレーテッド | 多相核酸増幅 |
CN104250663B (zh) * | 2013-06-27 | 2017-09-15 | 北京大学 | 甲基化CpG岛的高通量测序检测方法 |
CN103981278B (zh) * | 2014-06-06 | 2015-08-19 | 黑龙江出入境检验检疫局检验检疫技术中心 | 利用Tem-PCR技术检测多种致病菌的PCR检测通用引物对 |
CN108603224B (zh) | 2015-12-16 | 2022-06-28 | 富鲁达公司 | 高水平多路复用扩增 |
CN105543410B (zh) * | 2015-12-25 | 2019-06-07 | 四川农业大学 | 基于tem-pcr和基因芯片检测猪病毒性疾病的方法 |
CN106834546A (zh) * | 2017-03-20 | 2017-06-13 | 杭州迪安医学检验中心有限公司 | 一种基于熔解曲线法单管同时检测多种呼吸道病毒的引物及其应用 |
US20180340214A1 (en) * | 2017-05-25 | 2018-11-29 | Diatherix Laboratories, Inc. | Quantitative multiplex polymerase chain reaction in two reactions |
CN111206081B (zh) * | 2018-11-21 | 2023-06-30 | 思纳福(苏州)生命科技有限公司 | 核酸检测微球、制备方法、试剂盒及高通量核酸检测方法 |
CN109609615A (zh) * | 2018-12-06 | 2019-04-12 | 云南中医学院 | 一种缺血性脑卒中miRNA标记物的检测方法 |
CN109609693A (zh) * | 2018-12-26 | 2019-04-12 | 山东艾克韦生物技术有限公司 | 一种同时检测多种肠道病毒的方法 |
CN109913592A (zh) * | 2019-04-30 | 2019-06-21 | 广西大学 | ENTV-2的SYBR GreenⅠ荧光定量PCR检测引物对及诊断试剂盒 |
CN112593011A (zh) * | 2020-12-25 | 2021-04-02 | 中山大学 | 一组检测柯萨奇病毒b组的引物和探针 |
CN113637799B (zh) * | 2021-08-12 | 2023-09-29 | 北京农业生物技术研究中心 | 一种菊花b病毒的rpa检测方法 |
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KR100189229B1 (ko) | 1993-07-23 | 1999-06-01 | 다니엘 엘. 캐시앙, 헨리 엘. 노르호프 | 핵산 증폭을 강화하는 방법 |
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US5642825A (en) * | 1995-08-21 | 1997-07-01 | Superseal Corporation | Container closure having peripheral tamper-indicator |
GB9609441D0 (en) * | 1996-05-04 | 1996-07-10 | Zeneca Ltd | Process |
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JP2005509440A (ja) * | 2001-11-19 | 2005-04-14 | パラレル バイオサイエンス, インコーポレイテッド | 多重オリゴヌクレオチド付加および標的増幅 |
EP1468117A2 (en) | 2002-01-15 | 2004-10-20 | MATFORSK, Norwegian Food Research Institute | Methods of nucleic acid amplification |
EP1474529B1 (en) | 2002-02-08 | 2008-10-22 | Olympus Corporation | Specific multiplex analysis of nucleic acids |
-
2004
- 2004-10-13 BR BRPI0415435-5A patent/BRPI0415435A/pt not_active IP Right Cessation
- 2004-10-13 CN CN200480037162.7A patent/CN1898395B/zh not_active Expired - Fee Related
- 2004-10-13 AU AU2004282555A patent/AU2004282555B2/en not_active Ceased
- 2004-10-13 CA CA2542787A patent/CA2542787C/en not_active Expired - Lifetime
- 2004-10-13 US US10/575,804 patent/US7851148B2/en active Active
- 2004-10-13 WO PCT/US2004/033818 patent/WO2005038039A2/en active Application Filing
- 2004-10-13 KR KR1020067009208A patent/KR100830623B1/ko not_active Expired - Fee Related
- 2004-10-13 EP EP04795037A patent/EP1687437A4/en not_active Ceased
- 2004-10-13 JP JP2006535636A patent/JP4999460B2/ja not_active Expired - Fee Related
- 2004-10-13 NZ NZ546903A patent/NZ546903A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
WO2005038039A2 (en) | 2005-04-28 |
CA2542787A1 (en) | 2005-04-28 |
CA2542787C (en) | 2013-10-29 |
KR100830623B1 (ko) | 2008-05-20 |
US7851148B2 (en) | 2010-12-14 |
US20070141575A1 (en) | 2007-06-21 |
KR20060088128A (ko) | 2006-08-03 |
NZ546903A (en) | 2009-06-26 |
EP1687437A2 (en) | 2006-08-09 |
JP4999460B2 (ja) | 2012-08-15 |
WO2005038039A3 (en) | 2006-09-28 |
CN1898395A (zh) | 2007-01-17 |
EP1687437A4 (en) | 2008-01-02 |
CN1898395B (zh) | 2014-02-12 |
AU2004282555A1 (en) | 2005-04-28 |
JP2007508824A (ja) | 2007-04-12 |
AU2004282555B2 (en) | 2009-05-28 |
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