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Serotype-specific identification of enterovirus 71 by RT-PCR

机译:通过RT-PCR对肠道病毒71型进行血清型特异性鉴定

摘要

The present invention provides nucleic acids which can be used as primers in amplification or sequencing reactions to rapidly amplify or sequence, respectively, EV71 nucleic acids. A preferred group of nucleic acids of the present invention when used as primer pairs in amplification reactions, detect EV71 with a high degree of specifically and sensitivity. With these preferred primer pairs, the specificity of amplification methods of the present invention is such that EV71 nucleic acid is amplified to a detectable level, whereas CA16 DNA is not. The nucleic acid primers of the present invention contain mixed bases or deoxyinosine residues at positions of codon degeneracy. Examples of nucleic acid primers for amplifying and sequencing EV71 nucleic acid are set forth in the Sequence Listing as SEQ ID NOS:1-12. Examples of preferred primers for discriminating between EV71 and CA16 are set forth in the Sequence Listing as SEQ ID NOS:1-4.
机译:本发明提供了可用作扩增或测序反应中的引物以分别快速扩增或测序EV71核酸的核酸。当在扩增反应中用作引物对时,本发明的优选核酸组以高度特异性和灵敏度检测EV71。利用这些优选的引物对,本发明的扩增方法的特异性使得EV71核酸被扩增至可检测的水平,而CA16 DNA未被扩增。本发明的核酸引物在密码子简并性位置上含有混合碱基或脱氧肌苷残基。用于扩增和测序EV71核酸的核酸引物的实例在序列表中以SEQ ID NO:1-12列出。用于区分EV71和CA16的优选引物的实例在序列表中以SEQ ID NOS:1-4列出。

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