AR109017A1 - Métodos para utilizar polinucleótidos largos de adn simple cadena como cebadores (primers) en ensayos de pcr - Google Patents

Métodos para utilizar polinucleótidos largos de adn simple cadena como cebadores (primers) en ensayos de pcr

Info

Publication number
AR109017A1
AR109017A1 ARP170101919A ARP170101919A AR109017A1 AR 109017 A1 AR109017 A1 AR 109017A1 AR P170101919 A ARP170101919 A AR P170101919A AR P170101919 A ARP170101919 A AR P170101919A AR 109017 A1 AR109017 A1 AR 109017A1
Authority
AR
Argentina
Prior art keywords
nucleic acid
primers
polyucleotides
methods
single chain
Prior art date
Application number
ARP170101919A
Other languages
English (en)
Inventor
Martn Eduardo Mautner
Original Assignee
Mautner Martin Eduardo
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 Mautner Martin Eduardo filed Critical Mautner Martin Eduardo
Publication of AR109017A1 publication Critical patent/AR109017A1/es

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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
    • 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
    • C12Q1/6858Allele-specific amplification

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Molecular Biology (AREA)
  • Immunology (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Biophysics (AREA)
  • Physics & Mathematics (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

Método para realizar un ensayo de PCR que comprende los siguientes pasos: a) obtener una muestra de ácido nucleico; b) hibridizar dicha muestra de ácido nucleico a uno o más pares de primers donde al menos un primer consiste en un polinucleótido de ADN simple cadena de 60 o más nucleótidos; c) someter dicha muestra de ácido nucleico a una PCR donde el medio de la muestra de reacción contiene al menos uno de dichos primers; y d) detectar la longitud de los productos amplificados. El ácido nucleico amplificado puede contener cualquier secuencia o múltiples secuencias de repeticiones cortas en tándem (STRs, Short Tandem Repeats), genes o cualquier región codificante que tenga una ubicación definida en el genoma. Las muestras de ácido nucleico preferidas para ser amplificadas están degradadas o fragmentadas y contienen uno o más marcadores genéticos.
ARP170101919A 2016-07-12 2017-07-11 Métodos para utilizar polinucleótidos largos de adn simple cadena como cebadores (primers) en ensayos de pcr AR109017A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201662361184P 2016-07-12 2016-07-12

Publications (1)

Publication Number Publication Date
AR109017A1 true AR109017A1 (es) 2018-10-17

Family

ID=60941961

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP170101919A AR109017A1 (es) 2016-07-12 2017-07-11 Métodos para utilizar polinucleótidos largos de adn simple cadena como cebadores (primers) en ensayos de pcr

Country Status (5)

Country Link
US (1) US10822647B2 (es)
EP (1) EP3325671B1 (es)
CN (1) CN109477139B (es)
AR (1) AR109017A1 (es)
WO (1) WO2018011101A1 (es)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20200005894A1 (en) * 2018-06-29 2020-01-02 Rady Children's Hospital Research Center Method and system for sample identity assurance

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3834636A1 (de) 1988-10-11 1990-04-19 Max Planck Gesellschaft Verfahren zur analyse von laengenpolymorphismen in dna-bereichen
US5582979A (en) 1989-04-21 1996-12-10 Marshfield Clinic Length polymorphisms in (dC-dA)n.(dG-dT)n sequences and method of using the same
US5364759B2 (en) 1991-01-31 1999-07-20 Baylor College Medicine Dna typing with short tandem repeat polymorphisms and identification of polymorphic short tandem repeats
US6479235B1 (en) 1994-09-30 2002-11-12 Promega Corporation Multiplex amplification of short tandem repeat loci
DE10113265B4 (de) * 2001-03-16 2018-03-08 Qiagen Gmbh Verwendung einer stabilisierten Nukleinsäure zur Herstellung eines Proteins
US6743905B2 (en) 2001-04-16 2004-06-01 Applera Corporation Mobility-modified nucleobase polymers and methods of using same
CN101341258A (zh) * 2004-11-03 2009-01-07 第三次浪潮技术公司 单步检测测定法
CN101210240B (zh) * 2007-12-25 2011-11-16 天津大学 大引物pcr进行定点突变的方法
CN101818192B (zh) * 2009-08-27 2013-03-20 基点认知技术(北京)有限公司 20个短串联重复序列的复合扩增试剂盒
CN110777195A (zh) * 2012-07-13 2020-02-11 生命技术公司 采用一组snp的人身份识别
US9556482B2 (en) * 2013-07-03 2017-01-31 The United States Of America, As Represented By The Secretary Of Commerce Mouse cell line authentication
EP2860262A1 (en) 2013-10-09 2015-04-15 Universität Heidelberg Method for the quantitative analysis of nucleic acid fragmentation and amplifiability
RS61976B1 (sr) * 2014-02-18 2021-07-30 Illumina Inc Postupci i kompozicije za određivanje dnk profila

Also Published As

Publication number Publication date
WO2018011101A1 (en) 2018-01-18
US10822647B2 (en) 2020-11-03
EP3325671A1 (en) 2018-05-30
CN109477139B (zh) 2022-07-29
EP3325671B1 (en) 2022-10-26
CN109477139A (zh) 2019-03-15
US20180016621A1 (en) 2018-01-18

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