首页> 外国专利> A PRIMER FOR PCR AMPLIFICATION LINKED WITH COMPLEMENTARY SEQUENCES OR COMPLEMENTARY SEQUENCES INCLUDING MIS-MATCHED NUCLEOTIDES AND NUCLEIC ACID AMPLIFICATION METHOD USING THE SAME

A PRIMER FOR PCR AMPLIFICATION LINKED WITH COMPLEMENTARY SEQUENCES OR COMPLEMENTARY SEQUENCES INCLUDING MIS-MATCHED NUCLEOTIDES AND NUCLEIC ACID AMPLIFICATION METHOD USING THE SAME

机译:与扩增序列或包含错配核苷酸的互补序列或互补序列相关的互补序列的PCR扩增底漆

摘要

The present invention relates to a primer for PCR obtained by, directly or by using inosine as a linker, linking a complementary nucleotide sequence or a complementary nucleotide sequence including a mismatched nucleotide sequence to the 5-terminus of a forward or reverse primer; and to a PCR method comprising a step of mixing a nucleic acid template in a PCR composition containing the primer and then performing PCR on the mixture. The primer for PCR of the present invention comprises a complementary nucleotide sequence or a mismatched nucleotide sequence in a complementary nucleotide sequence, which is linked to the 5-terminus thereof directly or via a linker, thereby lowering the sensitivity increase due to the increase in amplification products and reducing non-specifically occurring reactions in PCR.
机译:本发明涉及用于PCR的引物,其通过直接或通过使用肌苷作为接头而获得,其将互补核苷酸序列或包括错配核苷酸序列的互补核苷酸序列连接至正向或反向引物的5末端。本发明涉及一种PCR方法,其包括以下步骤:将核酸模板混合在含有引物的PCR组合物中,然后对该混合物进行PCR。本发明的PCR用引物包含在互补核苷酸序列中的互补核苷酸序列或错配核苷酸序列,其直接或通过连接子连接至其5-末端,从而降低了由于扩增的增加而引起的灵敏度提高。产物和减少PCR中非特异性发生的反应。

著录项

  • 公开/公告号KR20160094113A

    专利类型

  • 公开/公告日2016-08-09

    原文格式PDF

  • 申请/专利权人 SD BIOSENSOR INC.;

    申请/专利号KR20150015276

  • 发明设计人 WON YOO DEOK;PARK HAE JOON;LEE SUN YOUNG;

    申请日2015-01-30

  • 分类号C12Q1/68;

  • 国家 KR

  • 入库时间 2022-08-21 14:13:48

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