CA2736621A1 - Amplification and detection reagents for hiv-1 - Google Patents
Amplification and detection reagents for hiv-1 Download PDFInfo
- Publication number
- CA2736621A1 CA2736621A1 CA2736621A CA2736621A CA2736621A1 CA 2736621 A1 CA2736621 A1 CA 2736621A1 CA 2736621 A CA2736621 A CA 2736621A CA 2736621 A CA2736621 A CA 2736621A CA 2736621 A1 CA2736621 A1 CA 2736621A1
- Authority
- CA
- Canada
- Prior art keywords
- seq
- sequence
- oligo
- hiv
- primer
- 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.)
- Abandoned
Links
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Classifications
-
- 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
- C12Q1/70—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving virus or bacteriophage
- C12Q1/701—Specific hybridization probes
- C12Q1/702—Specific hybridization probes for retroviruses
- C12Q1/703—Viruses associated with AIDS
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Immunology (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Analytical Chemistry (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Physics & Mathematics (AREA)
- AIDS & HIV (AREA)
- Biophysics (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)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/945,943 US6852491B2 (en) | 2001-09-04 | 2001-09-04 | Amplification and detection reagents for HIV-1 |
| US09/945,943 | 2001-09-04 | ||
| CA2459354A CA2459354C (en) | 2001-09-04 | 2002-07-12 | Amplification and detection reagents for hiv-1 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2459354A Division CA2459354C (en) | 2001-09-04 | 2002-07-12 | Amplification and detection reagents for hiv-1 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2736621A1 true CA2736621A1 (en) | 2003-03-13 |
Family
ID=25483738
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2736621A Abandoned CA2736621A1 (en) | 2001-09-04 | 2002-07-12 | Amplification and detection reagents for hiv-1 |
| CA2459354A Expired - Fee Related CA2459354C (en) | 2001-09-04 | 2002-07-12 | Amplification and detection reagents for hiv-1 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2459354A Expired - Fee Related CA2459354C (en) | 2001-09-04 | 2002-07-12 | Amplification and detection reagents for hiv-1 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US6852491B2 (enExample) |
| EP (3) | EP1430069A4 (enExample) |
| JP (3) | JP4413610B2 (enExample) |
| CA (2) | CA2736621A1 (enExample) |
| ES (1) | ES2458556T3 (enExample) |
| WO (1) | WO2003020878A2 (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU3219400A (en) * | 1999-02-03 | 2000-08-25 | Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services, The | Methods and reagents for molecular detection of hiv-1 groups m, n and |
| DE602005027809D1 (de) * | 2004-01-07 | 2011-06-16 | Hitachi Chemical Co Ltd | Primer und sonden zum nachweis von hiv |
| EP1602736A1 (en) * | 2004-06-04 | 2005-12-07 | Bio-Rad Pasteur | HIV type and subtype detection |
| EP1794327B1 (en) | 2004-09-14 | 2016-11-30 | Argos Therapeutics, Inc. | Strain independent amplification of pathogens and vaccines thereto |
| AU2011253599B2 (en) * | 2004-09-30 | 2013-12-12 | Gen-Probe Incorporated | Assay for detecting and quantifying HIV-1 |
| CA2582055C (en) * | 2004-09-30 | 2014-04-08 | Gen-Probe Incorporated | Assay for detecting and quantifying hiv-1 |
| WO2007065926A1 (en) * | 2005-12-07 | 2007-06-14 | Tibotec Pharmaceuticals Ltd. | Methods, plasmid vectors and primers for assessing hiv viral fitness |
| US20090061413A1 (en) * | 2006-02-27 | 2009-03-05 | Salinas Frank G | Isothermal screening of hiv-1 related nucleic acids |
| US8338101B2 (en) | 2007-01-23 | 2012-12-25 | Virco Bvba | Method for designing a drug regime for HIV-infected patients |
| US8221981B2 (en) * | 2007-07-30 | 2012-07-17 | Argos Therapeutics, Inc. | Primers and probes for the amplification and detection of HIV Gag, Rev and Nef polynucleotides |
| CA2639416C (en) * | 2007-09-11 | 2019-12-31 | F. Hoffmann-La Roche Ag | Diagnostic test for susceptibility to b-raf kinase inhibitors |
| US8724882B2 (en) * | 2008-07-29 | 2014-05-13 | Applied Materials Israel, Ltd. | Mapping variations of a surface |
| EP2436777B1 (en) | 2009-05-26 | 2015-08-19 | Xiamen University | Method for detecting variations in nucleic acid sequences |
| CN103069010B (zh) * | 2010-04-23 | 2016-02-24 | 基因组影像公司 | 通过由分子梳检测基因组和感染性病毒dna的病毒感染的诊断 |
| WO2013006684A1 (en) | 2011-07-05 | 2013-01-10 | The Gov. Of The U.S.A. As Represented By The Secretary Of The Dept. Of Health And Human Services. | Hiv-1 genotyping assay for global surveillance of hiv-1 drug resistance |
| EP2809784A4 (en) * | 2012-01-31 | 2015-07-15 | Advanced Liquid Logic Inc | AMPLIFICATION SPREADERS AND PROBES FOR DETECTING HIV-1 |
| JP6255353B2 (ja) | 2012-02-03 | 2017-12-27 | カリフォルニア インスティチュート オブ テクノロジー | 多重生化学アッセイにおける信号エンコードおよびデコード |
| EP2880184B1 (en) | 2012-08-03 | 2021-03-31 | California Institute of Technology | Multiplexing and quantification in pcr with reduced hardware and requirements |
| WO2014037712A2 (en) * | 2012-09-04 | 2014-03-13 | Genome Research Limited | Hiv-1 detection |
| WO2015118491A1 (en) * | 2014-02-06 | 2015-08-13 | University Of The Witwatersrand, Johannesburg | Method for detecting hiv |
| WO2017040520A1 (en) | 2015-08-31 | 2017-03-09 | Hitachi Chemical Co., Ltd. | Molecular methods for assessing urothelial disease |
| US10066263B2 (en) | 2016-06-17 | 2018-09-04 | California Institute Of Technology | Nucleic acid reactions and related methods and compositions |
| EP3781710A4 (en) | 2018-04-17 | 2022-01-05 | Chromacode, Inc. | METHODS AND SYSTEMS FOR MULTIPLEX ANALYSIS |
| US12203129B2 (en) | 2018-07-03 | 2025-01-21 | ChromaCode, Inc. | Formulations and signal encoding and decoding methods for massively multiplexed biochemical assays |
| US20220119787A1 (en) * | 2019-02-20 | 2022-04-21 | Biomedrex Ab | Virus therapy |
| KR102191513B1 (ko) | 2020-02-13 | 2020-12-15 | 주식회사 에스씨엘헬스케어 | Hiv-1 약제 내성 분석을 위한 프라이머 세트, 이를 포함하는 키트, 및 이를 이용한 분석 방법 |
| CN112795699A (zh) * | 2021-02-09 | 2021-05-14 | 南方医科大学 | 一种rt-raa荧光法检测hiv-1病毒不同亚型通用引物、探针及检测方法 |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4948882A (en) | 1983-02-22 | 1990-08-14 | Syngene, Inc. | Single-stranded labelled oligonucleotides, reactive monomers and methods of synthesis |
| US5034506A (en) | 1985-03-15 | 1991-07-23 | Anti-Gene Development Group | Uncharged morpholino-based polymers having achiral intersubunit linkages |
| DE3687030T2 (de) | 1985-03-15 | 1993-03-11 | Eugene Stirchak | Stereoregulare polynukleotiden bindende polymere. |
| US5185444A (en) | 1985-03-15 | 1993-02-09 | Anti-Gene Deveopment Group | Uncharged morpolino-based polymers having phosphorous containing chiral intersubunit linkages |
| US4683195A (en) | 1986-01-30 | 1987-07-28 | Cetus Corporation | Process for amplifying, detecting, and/or-cloning nucleic acid sequences |
| US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
| US5310652A (en) | 1986-08-22 | 1994-05-10 | Hoffman-La Roche Inc. | Reverse transcription with thermostable DNA polymerase-high temperature reverse transcription |
| US5322770A (en) | 1989-12-22 | 1994-06-21 | Hoffman-Laroche Inc. | Reverse transcription with thermostable DNA polymerases - high temperature reverse transcription |
| US6004826A (en) * | 1988-07-20 | 1999-12-21 | David Segev | Repair-mediated process for amplifying and detecting nucleic acid sequences |
| CA2003383A1 (en) * | 1988-11-23 | 1990-05-23 | Sushil G. Devare | Synthetic dna derived recombinant hiv antigens |
| ES2066887T3 (es) * | 1989-02-03 | 1995-03-16 | Abbott Lab | Anticuerpo monoclonal para diferenciar individuos seropositivos hiv-2 de los hiv-1. |
| SG47868A1 (en) * | 1989-06-02 | 1998-04-17 | Pasteur Institut | Nucleotide sequences erived from the genome of hiv-1 hiv-2 and siv type retroviruses and their applications especially for the amplification of the genomes of these (pls see pf1 for |
| CA2020958C (en) | 1989-07-11 | 2005-01-11 | Daniel L. Kacian | Nucleic acid sequence amplification methods |
| US5210015A (en) | 1990-08-06 | 1993-05-11 | Hoffman-La Roche Inc. | Homogeneous assay system using the nuclease activity of a nucleic acid polymerase |
| DK51092D0 (da) | 1991-05-24 | 1992-04-15 | Ole Buchardt | Oligonucleotid-analoge betegnet pna, monomere synthoner og fremgangsmaade til fremstilling deraf samt anvendelser deraf |
| US5464746A (en) | 1991-12-17 | 1995-11-07 | Abbott Laboratories | Haptens, tracers, immunogens and antibodies for carbazole and dibenzofuran derivatives |
| US5424414A (en) | 1991-12-17 | 1995-06-13 | Abbott Laboratories | Haptens, tracers, immunogens and antibodies for 3-phenyl-1-adamantaneacetic acids |
| JPH08503600A (ja) | 1992-05-29 | 1996-04-23 | アボツト・ラボラトリーズ | Ｒｎａ配列で開始させるリガーゼ連鎖反応 |
| EP2423322A1 (en) * | 1993-11-12 | 2012-02-29 | PHRI Properties, Inc. | Hybridization probes for nucleic acid detection, universal stems, methods and kits |
| US5925517A (en) | 1993-11-12 | 1999-07-20 | The Public Health Research Institute Of The City Of New York, Inc. | Detectably labeled dual conformation oligonucleotide probes, assays and kits |
| US5733781A (en) * | 1994-07-19 | 1998-03-31 | Gen-Probe Incorporated | Oligonucleotides and methods for inhibiting propagation of human immunodeficiency virus |
| US5962665A (en) | 1997-06-16 | 1999-10-05 | Abbott Laboratories | Nucleic acid primers and probes for detecting HIV-1 and HIV-2 |
| US6001558A (en) * | 1997-06-25 | 1999-12-14 | Ortho Clinical Diagnostics, Inc. | Amplification and detection of HIV-1 and/or HIV 2 |
| US6391544B1 (en) * | 1998-05-15 | 2002-05-21 | Abbott Laboratories | Method for using unequal primer concentrations for generating nucleic acid amplification products |
| DE19850186A1 (de) * | 1998-10-30 | 2000-05-25 | Roche Diagnostics Gmbh | Neue Primer und Sonden zum Nachweis von HIV |
| AU3219400A (en) * | 1999-02-03 | 2000-08-25 | Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services, The | Methods and reagents for molecular detection of hiv-1 groups m, n and |
| US6300075B1 (en) * | 1999-02-03 | 2001-10-09 | Ortho-Clinical Diagnostics, Inc | Enhancement of the specificity of nucleic acid amplification by carrier nucleic acid |
| AU781934B2 (en) * | 1999-07-09 | 2005-06-23 | Gen-Probe Incorporated | Detection of HIV-1 by nucleic acid amplification |
| AU781570B2 (en) * | 1999-07-23 | 2005-06-02 | Gen-Probe Incorporated | Polynucleotide amplification method |
| US6936414B2 (en) * | 1999-12-22 | 2005-08-30 | Abbott Laboratories | Nucleic acid isolation method and kit |
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2001
- 2001-09-04 US US09/945,943 patent/US6852491B2/en not_active Expired - Fee Related
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2002
- 2002-07-12 CA CA2736621A patent/CA2736621A1/en not_active Abandoned
- 2002-07-12 CA CA2459354A patent/CA2459354C/en not_active Expired - Fee Related
- 2002-07-12 EP EP02750006A patent/EP1430069A4/en not_active Withdrawn
- 2002-07-12 EP EP11154847.5A patent/EP2390259B1/en not_active Expired - Lifetime
- 2002-07-12 ES ES11154847.5T patent/ES2458556T3/es not_active Expired - Lifetime
- 2002-07-12 EP EP11154836A patent/EP2385144A1/en not_active Withdrawn
- 2002-07-12 JP JP2003525582A patent/JP4413610B2/ja not_active Expired - Fee Related
- 2002-07-12 WO PCT/US2002/022230 patent/WO2003020878A2/en not_active Ceased
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2009
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2012
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Also Published As
| Publication number | Publication date |
|---|---|
| EP1430069A4 (en) | 2007-04-04 |
| EP2390259B1 (en) | 2014-03-05 |
| WO2003020878A3 (en) | 2004-01-29 |
| CA2459354C (en) | 2011-06-14 |
| JP2009291202A (ja) | 2009-12-17 |
| US6852491B2 (en) | 2005-02-08 |
| US20030148280A1 (en) | 2003-08-07 |
| CA2459354A1 (en) | 2003-03-13 |
| ES2458556T3 (es) | 2014-05-06 |
| JP2005507655A (ja) | 2005-03-24 |
| EP1430069A2 (en) | 2004-06-23 |
| EP2390259A2 (en) | 2011-11-30 |
| JP5205346B2 (ja) | 2013-06-05 |
| JP4413610B2 (ja) | 2010-02-10 |
| WO2003020878A2 (en) | 2003-03-13 |
| EP2390259A3 (en) | 2012-05-02 |
| EP2385144A1 (en) | 2011-11-09 |
| JP2013063072A (ja) | 2013-04-11 |
| HK1164326A1 (en) | 2012-09-21 |
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