首页> 外国专利> Control primer annealing to improve the specificity of annealing in nucleic acid amplification, kit, methods for amplifying nucleic acid sequences of DNA and sequence of target nucleic acid or a mixture of nucleic acids, to detect the complementari Dade of DNA to mRNA differentially expressed in two or more samples of nucleic acid.To amplify a fragment of the cDNA target quickly, to amplify a population of cDNAs of filament double full-length complementary to mRNAs cDNAs, and filament double fortified with 5 'complementary to mRNAs to amplify rather than a sequence of nucleotide al VO at the same time, to produce a digital printing gDNA DNA, and RNA in a sample of mRNA.To identify segments of homology is conserved in a multigene family from a sample of mRNA, to identify a variation of nucleotide in a target nucleic acid, for mutagenesis in a target nucleic acid, and use of the initiator

Control primer annealing to improve the specificity of annealing in nucleic acid amplification, kit, methods for amplifying nucleic acid sequences of DNA and sequence of target nucleic acid or a mixture of nucleic acids, to detect the complementari Dade of DNA to mRNA differentially expressed in two or more samples of nucleic acid.To amplify a fragment of the cDNA target quickly, to amplify a population of cDNAs of filament double full-length complementary to mRNAs cDNAs, and filament double fortified with 5 'complementary to mRNAs to amplify rather than a sequence of nucleotide al VO at the same time, to produce a digital printing gDNA DNA, and RNA in a sample of mRNA.To identify segments of homology is conserved in a multigene family from a sample of mRNA, to identify a variation of nucleotide in a target nucleic acid, for mutagenesis in a target nucleic acid, and use of the initiator

机译:控制引物退火以改善核酸扩增中退火的特异性,试剂盒,扩增DNA核酸序列和靶核酸序列或核酸混合物的方法,检测DNA与mRNA互补表达的互补性(两种)或更多核酸样品。要快速扩增cDNA靶标的片段,以扩增与mRNA cDNA互补的长丝两倍全长的cDNA群体,并用与mRNA互补的5'双重修饰的长丝进行扩增而不是序列同时鉴定一个核苷酸的VO片段,以产生一个数字印刷的gDNA DNA和一个mRNA样品中的RNA。从一个mRNA样品中鉴定一个多基因家族中的同源片段是保守的,以鉴定一个核苷酸中一个核苷酸的变异。靶核酸,用于在靶核酸中诱变,以及引发剂的用途

摘要

"Control primer annealing to improve the specificity of annealing in nucleic acid amplification kit.Methods for amplifying a nucleic acid sequence of a DNA or a mixture of nucleic acids.And for selectively amplifying a nucleic acid sequence of a target DNA or a mixture of nucleic acids, and a sequence of the target nucleic acid from a mRNA.Method for detecting the complementarity of DNA to mRNA differentially expressed in two or more samples of nucleic acid, methods for amplifying a fragment of the cDNA and DNA quickly target.And to amplify a population of cDNAs of filament double full-length complementary to mRNAs cDNAs, and filament double fortified with 5 39 complementary to mRNAs,Method to amplify rather than a sequence of nucleotu00ecdeo target, at the same time, methods for producing a digital printing gDNA DNA and RNA of a sample of mRNA.Method for identifying segments of homology is conserved in a family of multigene from a sample of mRNA, a method for the mutagenesis in a target nucleic acid, and use of the initiator.The present invention relates to an annealing control primer annealing to improve the specificity of the amplification of nucleic acid and its applications in all fields of tecnoloGIA involved in nucleic acid amplification.This initiator comprises (a) a portion of the extremity 3 39 having a sequ00b3u00eancia nucleotide hibridizadora substantially complementary to a site in a nucleic acid standard for hibridizThe air with the same; (b) a portion of the tip 5 39 having a nucleotide sequ00b3u00eancia arbitrary pre selected; and (c) a regulating portion positioned between said portion of the extremity 3 and 39That portion of the extremity 5 39 comprising at least a universal basis or analogue non discriminatory basis.By means of which the said portion is capable of regulating a regulating portion of the annealing of said initiator in combination with the annealing temperature.
机译:控制引物退火,以提高核酸扩增试剂盒中退火的特异性。扩增DNA或核酸混合物的核酸序列的方法。以及选择性扩增靶DNA或核酸混合物的核酸序列的方法。核酸,以及来自mRNA的靶核酸序列。检测DNA与两个或多个核酸样品中差异表达的mRNA的互补性的方法,扩增cDNA和DNA片段的方法快速靶向。扩增与mRNA cDNA全长互补的双丝的cDNA群体,并用与mRNA互补的5 <39>双重增强的双丝,同时扩增核苷酸靶序列的方法,而不是核苷酸靶序列, mRNA样本的数字印刷gDNA DNA和RNA。从mRNA样本的多基因家族中鉴定同源片段的方法是保守的,这是一种诱变方法。退火控制引物退火技术,其用于改善核酸扩增的特异性及其在涉及核酸扩增的tecnoloGIA的所​​有领域中的应用。本发明涉及退火控制引物退火。 )末端3> <39的一部分,其seq u00b3 u00eancia核苷酸hibridizadora基本上与用于hibridiz的核酸标准中的位点互补。 (b)尖端5 <39>的一部分,其具有任意预先选择的核苷酸seq u00b3 u00eancia; (c)位于末端3>和<39的所述部分之间的调节部分,末端5> <39的该部分至少包括通用基础或类似的非歧视基础。通过这种方式,所述部分能够调节所述引发剂的退火的调节部分结合退火温度。

著录项

  • 公开/公告号BRPI0214741B1

    专利类型

  • 公开/公告日2015-05-12

    原文格式PDF

  • 申请/专利权人 SEEGENE INC.;

    申请/专利号BR2002PI14741

  • 发明设计人 JONG-YOON CHUN;

    申请日2002-09-19

  • 分类号C12N15/11;C12Q1/68;C07H21/04;

  • 国家 BR

  • 入库时间 2022-08-21 15:16:14

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