首页> 外国专利> METHOD FOR UNIVERSAL DETECTION AND QUANTIFICATION OF MYCOPLASMA (MOLLICUTES) 16S RDNA BY QUANTITATIVE POLYMERASE CHAIN REACTION AMPLIFYING A 1.5 KILOBASE FRAGMENT

METHOD FOR UNIVERSAL DETECTION AND QUANTIFICATION OF MYCOPLASMA (MOLLICUTES) 16S RDNA BY QUANTITATIVE POLYMERASE CHAIN REACTION AMPLIFYING A 1.5 KILOBASE FRAGMENT

机译:1.5千碱基片段的定量聚合酶链反应通用检测和鉴定肌白蛋白(分子)16S RDNA的方法

摘要

The present invention relates to a method for detecting mycoplasma 16S rDNA 1.5 kilobase fragment amplified by quantitative PCR. One of the most critical limitation of the qPCR is the DNA fragment length to amplify. The existing qPCR methods does not permit the amplification of long DNA fragments. Here the inventors demonstrate for the first time the amplification of mycoplasma 16S rDNA 1.5 kilobase fragment using qPCR based on real- time polymerase chain reaction. In particular, the present invention relates to a method for universal detection and quantification of mycoplasma 16S rDNA 1.5 kilobase fragment in a sample comprising contacting said sample with degenerate primers amplified by quantitative PCR or qPCR and using a DNA loading probe.
机译:本发明涉及通过定量PCR扩增的支原体16S rDNA 1.5kb碱基片段的检测方法。 qPCR的最关键限制之一是要扩增的DNA片段长度。现有的qPCR方法不允许扩增长DNA片段。在这里,发明人首次证明了基于实时聚合酶链反应的qPCR扩增支原体16S rDNA 1.5 kb片段。特别地,本发明涉及用于样品中支原体16S rDNA 1.5kb碱基片段的通用检测和定量的方法,该方法包括使所述样品与通过定量PCR或qPCR扩增的简并引物接触,并使用DNA加载探针。

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