[go: up one dir, main page]

BRPI0415435A - método e kit para amplificação baseada em iniciador de ácidos nucleicos - Google Patents

método e kit para amplificação baseada em iniciador de ácidos nucleicos

Info

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
Application number
BRPI0415435-5A
Other languages
English (en)
Inventor
Jian Han
Original Assignee
Genaco Biomedical Products Inc
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 Genaco Biomedical Products Inc filed Critical Genaco Biomedical Products Inc
Publication of BRPI0415435A publication Critical patent/BRPI0415435A/pt

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
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6844Nucleic acid amplification reactions
    • C12Q1/686Polymerase chain reaction [PCR]
    • 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
    • C12Q2525/00Reactions involving modified oligonucleotides, nucleic acids, or nucleotides
    • C12Q2525/10Modifications characterised by
    • C12Q2525/155Modifications characterised by incorporating/generating a new priming site
    • 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
    • C12Q2527/00Reactions demanding special reaction conditions
    • C12Q2527/143Concentration of primer or probe
    • 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
    • C12Q2531/00Reactions of nucleic acids characterised by
    • C12Q2531/10Reactions of nucleic acids characterised by the purpose being amplify/increase the copy number of target nucleic acid
    • C12Q2531/113PCR
    • 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
    • C12Q2537/00Reactions characterised by the reaction format or use of a specific feature
    • C12Q2537/10Reactions characterised by the reaction format or use of a specific feature the purpose or use of
    • C12Q2537/143Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis
    • 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
    • C12Q2549/00Reactions characterised by the features used to influence the efficiency or specificity
    • C12Q2549/10Reactions characterised by the features used to influence the efficiency or specificity the purpose being that of reducing false positive or false negative signals
    • C12Q2549/119Reactions 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
    • 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
    • C12Q2565/00Nucleic acid analysis characterised by mode or means of detection
    • C12Q2565/10Detection mode being characterised by the assay principle
    • C12Q2565/102Multiple non-interacting labels
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against 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.
BRPI0415435-5A 2003-10-13 2004-10-13 método e kit para amplificação baseada em iniciador de ácidos nucleicos BRPI0415435A (pt)

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)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4683202A (en) * 1985-03-28 1987-07-28 Cetus Corporation Process for amplifying nucleic acid sequences
US5194300A (en) * 1987-07-15 1993-03-16 Cheung Sau W Methods of making fluorescent microspheres
JPH0491790A (ja) 1990-08-02 1992-03-25 Shionogi & Co Ltd 2段階pcr法
US5341809A (en) * 1990-08-31 1994-08-30 Hitachi, Ltd. Ultrasonic flowmeter
DE69213112T2 (de) * 1991-06-20 1997-04-03 Hoffmann La Roche Verbesserte Methoden zur Nukleinsäure-Amplifizierung
DE69230736T2 (de) * 1991-08-27 2000-06-21 Zeneca Ltd., London Verfahren zur Charakterisierung genomischer DNA
US5340728A (en) * 1992-12-09 1994-08-23 E. I. Du Pont De Nemours And Company Method for amplification of targeted segments of nucleic acid using nested polymerase chain reaction
US5422252A (en) 1993-06-04 1995-06-06 Becton, Dickinson And Company Simultaneous amplification of multiple targets
KR100189229B1 (ko) 1993-07-23 1999-06-01 다니엘 엘. 캐시앙, 헨리 엘. 노르호프 핵산 증폭을 강화하는 방법
US5882856A (en) * 1995-06-07 1999-03-16 Genzyme Corporation Universal primer sequence for multiplex DNA amplification
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
US6168917B1 (en) * 1996-10-02 2001-01-02 The United States Of America As Represented By The Department Of Health And Human Services Detection and identification of non-polio enteroviruses
AUPQ008799A0 (en) * 1999-04-30 1999-05-27 Tillett, Daniel Genome sequencing
US6509157B1 (en) * 1999-11-05 2003-01-21 Roche Molecular Systems, Inc 3 blocked nucleic acid amplification primers
US6605451B1 (en) 2000-06-06 2003-08-12 Xtrana, Inc. Methods and devices for multiplexing amplification reactions
US6566067B2 (en) * 2001-02-14 2003-05-20 Synthegen Systems, Inc. High fidelity PCR cloning
WO2002070728A2 (en) * 2001-03-01 2002-09-12 The Johns Hopkins University Quantitative assay for the simultaneous detection and speciation of bacterial infections
US7262030B2 (en) * 2001-05-09 2007-08-28 Virginia Commonwealth University Multiple sequencible and ligatible structures for genomic analysis
DE60216777T2 (de) * 2001-08-23 2007-10-31 Merck & Co., Inc. Multiplex-hpv-pcr-fluoreszenzassays unter verwendung mehrerer fluorophore
US20030096277A1 (en) * 2001-08-30 2003-05-22 Xiangning Chen Allele specific PCR for genotyping
US7153656B2 (en) * 2001-09-11 2006-12-26 Los Alamos National Security, Llc Nucleic acid sequence detection using multiplexed oligonucleotide PCR
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

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

Similar Documents

Publication Publication Date Title
BRPI0415435A (pt) método e kit para amplificação baseada em iniciador de ácidos nucleicos
Weinberg et al. Comparative genomics reveals 104 candidate structured RNAs from bacteria, archaea, and their metagenomes
ES2728743T3 (es) Flujo de trabajo para la detección de ligandos utilizando ácidos nucleicos
Yang et al. Development of an isothermoal amplification-based assay for rapid visual detection of an Orf virus
FI3587587T3 (fi) Koostumuksia ja menetelmiä nukleiinihapposekvenssin kvantifioimiseksi näytteessä
WO2005106040A3 (en) Method and device for sample preparation control
ES2770638T3 (es) Nuevas composiciones, métodos y kits para la reacción en cadena de la polimerasa (PCR)
Ranjan et al. Development and evaluation of a one step reverse transcription-loop mediated isothermal amplification assay (RT-LAMP) for rapid detection of foot and mouth disease virus in India
CN105349683B (zh) 目标物保护的哑铃分子探针介导的级联滚环扩增策略用于dna甲基转移酶活性的灵敏检测
BRPI0816047A2 (pt) conjunto de oligonucleotídeos para detecção de um ácido nucleico alvo, métodos para detecção da presença ou ausência de um ácido nucleico alvo e de pelo menos dois ácidos nucleicos alvo, kit, mistura de reação e amplicon identificado por fluorescência
ATE538216T1 (de) Nukleinsäureverstärkung mithilfe eines reversibel modifizierten oligonukleotids
ES2767331T3 (es) Composiciones y procedimientos para la detección de Clostridium difficile
CN116287433A (zh) 一种高灵敏度猴痘病毒检测试剂盒及检测方法
BR0207914A (pt) Método para a amplificação baseada em transcrição de uma sequência de ácido nucleico alvo partindo de dna opcionalmente presente em uma amostra
ES2601898T3 (es) Supresión de amplificación no específica
EP1634962A4 (en) METHOD FOR DETECTING TARGET NUCLEOTIDE SEQUENCE, TARGET DETECTION STRUCTURE FOR USE IN IMPLEMENTING THE SAME, METHOD FOR PRODUCING THE SAME, AND ANALYSIS KIT FOR DETECTING TARGET NUCLEOTIDE SEQUENCE
WO2022040443A3 (en) A rapid diagnostic test for lamp
ES2993457T3 (en) A substrate for a nicking and extension reaction comprising a nucleic acid duplex
CN102041317A (zh) 基于g4dna酶显色的可视化基因鉴别检测试剂的制备方法
CN107058517A (zh) 一种用于结核分枝杆菌感染检测的试剂盒及检测方法
Amsailale et al. Protein phosphatase 2A regulates deoxycytidine kinase activity via Ser-74 dephosphorylation
BRPI0207893B8 (pt) método para a amplificação com base em transcrição de uma seqüência de ácido nucléico do hbv de filamento duplo alvo partindo do dna do hbv opcionalmente presente em uma amostra, oligonucleotídeo, e, conjunto de teste adequado para realizar a amplificação e detecção com base em transcrição de dna do hbv
US20230313323A1 (en) Assays for detecting coronavirus disease 2019 (covid-19)
Das et al. Differential kinetics at PK/PEPCK branch point in the cestode, Raillietina echinobothrida
Veledo et al. Protein fingerprinting of Staphylococcus species by capillary electrophoresis with on-capillary derivatization and laser-induced fluorescence detection

Legal Events

Date Code Title Description
B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

Free format text: REFERENTE A 7A ANUIDADE(S)

B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]

Free format text: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 2129 DE 25/10/2011.