JP2015507930A5 - - Google Patents

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Publication number
JP2015507930A5
JP2015507930A5 JP2014557769A JP2014557769A JP2015507930A5 JP 2015507930 A5 JP2015507930 A5 JP 2015507930A5 JP 2014557769 A JP2014557769 A JP 2014557769A JP 2014557769 A JP2014557769 A JP 2014557769A JP 2015507930 A5 JP2015507930 A5 JP 2015507930A5
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JP
Japan
Prior art keywords
nucleic acid
atn
thio
amino
dna polymerase
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JP2014557769A
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English (en)
Japanese (ja)
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JP6225123B2 (ja
JP2015507930A (ja
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Priority claimed from US13/446,474 external-priority patent/US9353393B2/en
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Publication of JP2015507930A5 publication Critical patent/JP2015507930A5/ja
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Publication of JP6225123B2 publication Critical patent/JP6225123B2/ja
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JP2014557769A 2012-02-15 2013-02-14 非特異的核酸増幅を低減するための方法及びキット Active JP6225123B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201261599119P 2012-02-15 2012-02-15
US61/599,119 2012-02-15
US13/446,474 2012-04-13
US13/446,474 US9353393B2 (en) 2012-02-15 2012-04-13 Methods and kits for reducing non-specific nucleic acid amplification
PCT/US2013/026136 WO2013123187A1 (en) 2012-02-15 2013-02-14 Methods and kits for reducing non-specific nucleic acid amplification

Publications (3)

Publication Number Publication Date
JP2015507930A JP2015507930A (ja) 2015-03-16
JP2015507930A5 true JP2015507930A5 (OSRAM) 2017-08-03
JP6225123B2 JP6225123B2 (ja) 2017-11-01

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ID=48945882

Family Applications (1)

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JP2014557769A Active JP6225123B2 (ja) 2012-02-15 2013-02-14 非特異的核酸増幅を低減するための方法及びキット

Country Status (6)

Country Link
US (1) US9353393B2 (OSRAM)
EP (1) EP2814976B1 (OSRAM)
JP (1) JP6225123B2 (OSRAM)
CN (1) CN104093850B (OSRAM)
CA (1) CA2864676C (OSRAM)
WO (1) WO2013123187A1 (OSRAM)

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EP2877593B1 (en) 2012-07-26 2018-07-18 Illumina, Inc. Compositions and methods for the amplification of nucleic acids
US9938568B2 (en) 2013-07-26 2018-04-10 General Electric Company Ligase-assisted nucleic acid circularization and amplification
US9587263B2 (en) * 2014-03-26 2017-03-07 General Electric Company Isothermal amplification under low salt condition
US10683534B2 (en) * 2015-01-27 2020-06-16 BioSpyder Technologies, Inc. Ligation assays in liquid phase
WO2016053638A1 (en) * 2014-09-30 2016-04-07 Ge Healthcare Bio-Sciences Corp. Method for nucleic acid analysis directly from an unpurified biological sample
CN108473932B (zh) 2015-09-09 2022-07-15 集联健康有限公司 用于样品收集、稳定化和保存的系统、方法和装置
US10077459B2 (en) * 2016-05-04 2018-09-18 General Electric Company Cell-free protein expression using rolling circle amplification product
WO2018209092A1 (en) * 2017-05-10 2018-11-15 Board Of Regents, The University Of Texas System Methods and devices related to amplifying nucleic acid at a variety of temperatures
US11001868B2 (en) * 2017-08-11 2021-05-11 Global Life Sciences Solutions Operations UK Ltd Cell-free protein expression using double-stranded concatameric DNA
CN111334562A (zh) * 2018-12-19 2020-06-26 合肥铼科生物科技有限公司 一种含有修饰引物的核酸扩增方法和试剂盒
CN110295241A (zh) * 2019-07-11 2019-10-01 深圳易致生物科技有限公司 用于检测尿路感染的引物组和包含该引物组的试剂盒
FR3110602B1 (fr) 2020-05-20 2025-03-07 Anova Plus Methode de detection sur le terrain de la presence et de la mutliresistance d’un bio-agresseur, notamment dezymo-septoria tritici,dans des culturescerealieres
CN112899346A (zh) * 2021-01-05 2021-06-04 南京普济生物有限公司 一种降低pcr非特异性扩增的核苷酸及其设计方法与应用
FR3129407B1 (fr) 2021-11-25 2024-12-13 Anova Plus Methode de detection de la presence d’un pathogene et determination de ses caracteristiques en sante humaine et animale
CN114277103A (zh) * 2022-01-21 2022-04-05 杭州飞时达生物科技有限公司 一种基于六聚体随机引物高效滚环扩增方法

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040086880A1 (en) * 1999-07-20 2004-05-06 Sampson Jeffrey R Method of producing nucleic acid molecules with reduced secondary structure
WO2002042490A1 (en) 2000-11-24 2002-05-30 Asper OÜ Method of optimising the sequences of synthetic nucleic acids
US7993839B2 (en) * 2001-01-19 2011-08-09 General Electric Company Methods and kits for reducing non-specific nucleic acid amplification
US20020197618A1 (en) * 2001-01-20 2002-12-26 Sampson Jeffrey R. Synthesis and amplification of unstructured nucleic acids for rapid sequencing
US6617137B2 (en) 2001-10-15 2003-09-09 Molecular Staging Inc. Method of amplifying whole genomes without subjecting the genome to denaturing conditions
US20030165859A1 (en) * 2001-10-23 2003-09-04 Invitrogen Corporation Primers and methods for the detection and discrimination of nucleic acids
US7176002B2 (en) 2002-05-16 2007-02-13 Applera Corporation Universal-tagged oligonucleotide primers and methods of use
EP1426448A1 (en) 2002-12-03 2004-06-09 bioMérieux BV Method for lowering the effects of sequence variations in a diagnostic hybridization assay, probe for use in the assay and assay
US8871469B1 (en) 2004-11-13 2014-10-28 Steven Albert Benner Self-avoiding molecular recognition systems in DNA priming
CN101213311B (zh) 2005-04-29 2013-02-13 合成基因组股份有限公司 利用滚环扩增扩增和克隆单个dna分子
DE602007013223D1 (de) 2006-06-01 2011-04-28 Trilink Biotechnologies San Diego Chemisch modifizierte oligonukleotidprimer zur nukleinsäureamplifikation
AU2008272421B2 (en) 2007-07-03 2014-09-04 Genaphora Ltd. Chimeric primers for improved nucleic acid amplification reactions
WO2009046149A1 (en) 2007-10-01 2009-04-09 Applied Biosystems Inc. Chase ligation sequencing
AU2010307991A1 (en) 2009-10-13 2012-05-10 Syntezza Molecular Detection Israel Ltd. Methods and compositions for amplifying target sequences from nucleic acid samples
US20110195457A1 (en) 2010-02-09 2011-08-11 General Electric Company Isothermal amplification of nucleic acid using primers comprising a randomized sequence and specific primers and uses thereof

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