首页> 外国专利> DUMBBELL- PCR: A METHOD TO QUANTIFY SPECIFIC SMALL RNA VARIANTS WITH A SINGLE NUCLEOTIDE RESOLUTION AT TERMINAL SEQUENCES

DUMBBELL- PCR: A METHOD TO QUANTIFY SPECIFIC SMALL RNA VARIANTS WITH A SINGLE NUCLEOTIDE RESOLUTION AT TERMINAL SEQUENCES

机译:DUMBBELL-PCR:一种在末端序列具有单个核苷酸分辨率的特定小RNA变异体的方法

摘要

A method for specifically and efficiently quantify the expression of targeted RNA variants with specific terminal sequences suitable to identify multiple isoforms bearing complex heterogeneity in terminal sequences by hybridizing a 5′-Dbs-adapter to the 5′-end of target RNAs, wherein the 5′-Dbs-adapter has a stem-loop structure whose protruding 5′-end base-pairs 5′-end of target RNAs, and wherein the loop region of 5′-Dbs-adapter contains a base-lacking spacer which will terminate reverse transcription in a subsequent step; hybridizing a 3′-Db-adapter to the 3′-end of target RNAs, wherein the 3′-Db-adapter has a stem-loop structure whose protruding 3′-end base-pairs 3′-end of target RNAs; ligating the both adapters with target RNAs by Rnl2 ligation to form “dumbbell-like” structure; and, amplifying and quantifying the ligation product by TaqMan RT-PCR.
机译:一种通过将5'-Dbs-衔接子与靶RNA的5'-末端杂交来特异性和有效地定量具有特定末端序列的靶向RNA变体表达的方法,该特定末端序列适合于鉴定在末端序列中具有复杂异质性的多种同工型,其中5 '-Dbs-衔接子具有茎环结构,其靶RNA的5'-末端碱基对的5'-末端突出,并且其中5'-Dbs-衔接子的环区域包含碱基缺失的间隔子,该间隔子将反向终止在后续步骤中转录;使3'-Db-衔接子与靶RNA的3'-末端杂交,其中所述3'-Db-衔接子具有茎环结构,其茎的突出的靶RNA的3'-端碱基对3'-端;通过Rnl2连接将两个衔接子与靶RNA连接,形成“哑铃状”结构;通过TaqMan RT-PCR扩增和定量连接产物。

著录项

  • 公开/公告号US2018251830A1

    专利类型

  • 公开/公告日2018-09-06

    原文格式PDF

  • 申请/专利权人 THOMAS JEFFERSON UNIVERSITY;

    申请/专利号US201615754194

  • 发明设计人 YOHEI KIRINO;SHOZO HONDA;

    申请日2016-08-22

  • 分类号C12Q1/6853;C12Q1/6851;C12Q1/6811;

  • 国家 US

  • 入库时间 2022-08-21 12:56:21

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