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SEROTYPE-SPECIFIC IDENTIFICATION OF ENTEROVIRUS 71 BY RT-PCR

机译:RT-PCR鉴定肠病毒71型

摘要

The present invention provides nucleic acids which can be used as primers inamplification or sequencing reactions to rapidly amplify or sequence,respectively, EV71 nucleic acids. A preferred group of nucleic acids of thepresent invention when used as primer pairs in amplification reactions, detectEV71 with a high degree of specifically and sensitivity. With these preferredprimer pairs, the specificity of amplification methods of the presentinvention is such that EV71 nucleic acid is amplified to a detectable level,whereas CA16 DNA is not. The nucleic acid primers of the present inventioncontain mixed bases or deoxyinosine residues at positions of codon degeneracy.Examples of nucleic acid primers for amplifying and sequencing EV71 nucleicacid are set forth in the Sequence Listing as SEQ ID NOS:1-12. Examples ofpreferred primers for discriminating between EV71 and CA16 are set forth inthe Sequence Listing as SEQ ID NOS:1-4.
机译:本发明提供了可用作引物的核酸。扩增或测序反应以快速扩增或测序,分别是EV71核酸。一组优选的核酸当本发明用作扩增反应中的引物对时,检测EV71具有高度的特异性和敏感性。有了这些首选引物对,本发明扩增方法的特异性发明是将EV71核酸扩增到可检测的水平,而CA16 DNA并非如此。本发明的核酸引物在密码子简并位置含有混合碱基或脱氧肌苷残基。用于扩增和测序EV71核酸的核酸引物的例子氨基酸在序列表中以SEQ ID NO:1-12列出。示例区分EV71和CA16的优选引物列于序列表为SEQ ID NOS:1-4。

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