SG11202007924TA - Method for introducing mutations - Google Patents

Method for introducing mutations

Info

Publication number
SG11202007924TA
SG11202007924TA SG11202007924TA SG11202007924TA SG11202007924TA SG 11202007924T A SG11202007924T A SG 11202007924TA SG 11202007924T A SG11202007924T A SG 11202007924TA SG 11202007924T A SG11202007924T A SG 11202007924TA SG 11202007924T A SG11202007924T A SG 11202007924TA
Authority
SG
Singapore
Prior art keywords
introducing mutations
mutations
introducing
Prior art date
Application number
SG11202007924TA
Inventor
Leigh G Monahan
Joyce To
Catherine M Burke
Michael Imelfort
Aaron E Darling
Original Assignee
Longas Tech Pty Ltd
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 Longas Tech Pty Ltd filed Critical Longas Tech Pty Ltd
Publication of SG11202007924TA publication Critical patent/SG11202007924TA/en

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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/66General methods for inserting a gene into a vector to form a recombinant vector using cleavage and ligation; Use of non-functional linkers or adaptors, e.g. linkers containing the sequence for a restriction endonuclease
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    • 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]
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    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/10Processes for the isolation, preparation or purification of DNA or RNA
    • C12N15/1034Isolating an individual clone by screening libraries
    • C12N15/1065Preparation or screening of tagged libraries, e.g. tagged microorganisms by STM-mutagenesis, tagged polynucleotides, gene tags
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    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/10Transferases (2.)
    • C12N9/12Transferases (2.) transferring phosphorus containing groups, e.g. kinases (2.7)
    • C12N9/1241Nucleotidyltransferases (2.7.7)
    • C12N9/1252DNA-directed DNA polymerase (2.7.7.7), i.e. DNA replicase
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    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
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    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
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    • C12Q1/6844Nucleic acid amplification reactions
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    • C12Q2521/00Reaction characterised by the enzymatic activity
    • C12Q2521/10Nucleotidyl transfering
    • C12Q2521/101DNA polymerase
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    • C12Q2525/00Reactions involving modified oligonucleotides, nucleic acids, or nucleotides
    • C12Q2525/10Modifications characterised by
    • C12Q2525/101Modifications characterised by incorporating non-naturally occurring nucleotides, e.g. inosine
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    • C12Q2525/00Reactions involving modified oligonucleotides, nucleic acids, or nucleotides
    • C12Q2525/10Modifications characterised by
    • C12Q2525/179Modifications characterised by incorporating arbitrary or random nucleotide sequences
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    • C12Q2525/00Reactions involving modified oligonucleotides, nucleic acids, or nucleotides
    • C12Q2525/10Modifications characterised by
    • C12Q2525/191Modifications characterised by incorporating an adaptor
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    • C12Q2525/00Reactions involving modified oligonucleotides, nucleic acids, or nucleotides
    • C12Q2525/10Modifications characterised by
    • C12Q2525/197Modifications characterised by incorporating a spacer/coupling moiety
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    • C12Q2527/137Concentration of a component of medium
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    • 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

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  • Chemical & Material Sciences (AREA)
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  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Molecular Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • General Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Biophysics (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Immunology (AREA)
  • Analytical Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Plant Pathology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Bioinformatics & Computational Biology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
SG11202007924TA 2018-02-20 2019-02-19 Method for introducing mutations SG11202007924TA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB1802744.1A GB201802744D0 (en) 2018-02-20 2018-02-20 Method
PCT/GB2019/050443 WO2019162657A1 (en) 2018-02-20 2019-02-19 Method for introducing mutations

Publications (1)

Publication Number Publication Date
SG11202007924TA true SG11202007924TA (en) 2020-09-29

Family

ID=61783821

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11202007924TA SG11202007924TA (en) 2018-02-20 2019-02-19 Method for introducing mutations

Country Status (12)

Country Link
US (2) US11421238B2 (en)
EP (2) EP4008792A1 (en)
JP (2) JP7413283B2 (en)
KR (1) KR20200123458A (en)
CN (1) CN112088219A (en)
AU (1) AU2019223315A1 (en)
CA (1) CA3091770A1 (en)
DK (1) DK3673084T3 (en)
ES (1) ES2889548T3 (en)
GB (1) GB201802744D0 (en)
SG (1) SG11202007924TA (en)
WO (1) WO2019162657A1 (en)

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5780231A (en) * 1995-11-17 1998-07-14 Lynx Therapeutics, Inc. DNA extension and analysis with rolling primers
WO2002079502A1 (en) 2001-03-28 2002-10-10 The University Of Queensland A method for nucleic acid sequence analysis
EP2292767B1 (en) 2004-06-04 2013-11-20 Takara Bio, Inc. Polypepdides having DNA polymerase activity
US9481912B2 (en) * 2006-09-12 2016-11-01 Longhorn Vaccines And Diagnostics, Llc Compositions and methods for detecting and identifying nucleic acid sequences in biological samples
JP5279339B2 (en) 2008-05-16 2013-09-04 タカラバイオ株式会社 Composition for reverse transcription reaction
EP2539464B1 (en) 2010-02-23 2016-11-16 Illumina, Inc. Amplification methods to minimise sequence specific bias
AU2011253984A1 (en) * 2010-12-07 2012-06-28 Biobalance Llc Method For Identifying E. Coli M-17
US9977861B2 (en) 2012-07-18 2018-05-22 Illumina Cambridge Limited Methods and systems for determining haplotypes and phasing of haplotypes
AU2015210705B2 (en) * 2014-01-31 2020-11-05 Integrated Dna Technologies, Inc. Improved methods for processing DNA substrates
CN104232761A (en) 2014-08-27 2014-12-24 武汉凯吉盈科技有限公司 Gene complete segment quick sequencing method
AU2015330685B2 (en) 2014-10-10 2022-02-17 Cold Spring Harbor Laboratory Random nucleotide mutation for nucleotide template counting and assembly
US10487340B2 (en) 2015-10-09 2019-11-26 Yunnan Academy Of Tobacco Agricultural Sciences Tobacco mosaic virus resistant N'au gene and cloning methods and applications thereof
CN107760771A (en) 2017-11-16 2018-03-06 杭州迪安医学检验中心有限公司 A kind of breast cancer susceptibility gene BRCA1 and BRCA2 full genomes capture primer, kit and its method
CN107955806B (en) 2017-12-15 2020-03-31 中国科学院深海科学与工程研究所 Preparation method and application of superoxide dismutase Cu, Zn SOD (superoxide dismutase) from deep-sea cucumber
AU2019366472A1 (en) 2018-10-26 2021-05-27 The Board Of Trustees Of The Leland Stanford Junior University Methods and uses of introducing mutations into genetic material for genome assembly

Also Published As

Publication number Publication date
JP7413283B2 (en) 2024-01-15
CN112088219A (en) 2020-12-15
EP4008792A1 (en) 2022-06-08
KR20200123458A (en) 2020-10-29
GB201802744D0 (en) 2018-04-04
US20210010008A1 (en) 2021-01-14
JP2021514205A (en) 2021-06-10
US20220348940A1 (en) 2022-11-03
EP3673084A1 (en) 2020-07-01
DK3673084T3 (en) 2021-11-08
EP3673084B1 (en) 2021-08-11
ES2889548T3 (en) 2022-01-12
CA3091770A1 (en) 2019-08-29
AU2019223315A1 (en) 2020-10-01
JP2024038164A (en) 2024-03-19
US11421238B2 (en) 2022-08-23
WO2019162657A1 (en) 2019-08-29

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