首页> 外国专利> 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 '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 in 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

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 '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 in 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

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用于检测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片段的方法可快速靶向。全长与mRNA cDNA互补的双细丝cDNA的cDNA群体,以及与mRNA互补的5'增强双细丝的cDNA,同时扩增而不是核苷酸靶序列的方法,产生数字印刷gDNA DNA的方法mRNA样品中的RNA和RNA.mRNA样品的多基因家族中用于鉴定同源片段的方法是保守的,这是一种在靶标中诱变的方法

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,其具有预先任意选择的核苷酸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BR0214741A

    专利类型

  • 公开/公告日2004-11-23

    原文格式PDF

  • 申请/专利权人 SEEGENE INC.;

    申请/专利号BR20020214741

  • 发明设计人 JONG-YOON CHUN;

    申请日2002-09-19

  • 分类号C12Q1/68;

  • 国家 BR

  • 入库时间 2022-08-21 22:18:44

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