首页> 外国专利> PCR PRIMER LINKED TO COMPLEMENTARY NUCLEOTIDE SEQUENCE OR COMPLEMENTARY NUCLEOTIDE SEQUENCE INCLUDING MIS-MATCHED NUCLEOTIDES AND METHOD FOR AMPLIFYING NUCLEIC ACID USING SAME

PCR PRIMER LINKED TO COMPLEMENTARY NUCLEOTIDE SEQUENCE OR COMPLEMENTARY NUCLEOTIDE SEQUENCE INCLUDING MIS-MATCHED NUCLEOTIDES AND METHOD FOR AMPLIFYING NUCLEIC ACID USING SAME

机译:连接到互补核苷酸序列或包括错误匹配的核苷酸的互补核苷酸序列的PCR引物,以及使用相同的核酸扩增核酸的方法

摘要

The present invention relates to a primer for PCR obtained by, directly or through inosine as a linker, linking a complementary nucleotide sequence or a complementary nucleotide sequence including a mis-matched nucleotide sequence to the 5'-terminal of a forward or reverse primer; and to a PCR method including a step of mixing a nucleic acid template in a PCR composition including the primer and then performing PCR on the mixture. The primer for PCR of the present invention includes a complementary nucleotide sequence or a mis-matched nucleotide sequence in a complementary nucleotide sequence, which is linked to the 5'-terminal 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,该引物是通过直接或通过肌苷作为接头而获得的,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:将核酸模板混合在包含引物的PCR组合物中,然后对该混合物进行PCR。本发明的用于PCR的引物包括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,其直接或通过接头连接至其5'-末端,从而降低了因增加扩增产物并减少PCR中非特异性发生的反应。

著录项

  • 公开/公告号EP3252168B1

    专利类型

  • 公开/公告日2020-10-07

    原文格式PDF

  • 申请/专利权人 SD BIOSENSOR INC.;

    申请/专利号EP20160743613

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

    申请日2016-01-07

  • 分类号C12Q1/6806;

  • 国家 EP

  • 入库时间 2022-08-21 11:42:19

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