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IDENTIFICATION AND QUANTIFICATION OF ONCOGENIC HPV NUCLEIC ACIDS BY MEANS OF REAL-TIME PCR ASSAYS

机译:实时荧光定量PCR检测致癌性HPV核酸的鉴定和定量

摘要

Method for the identification and quantification of oncogenic HPV nucleic acids comprising: a) first line screening by means of 5 independent SYBR Green I Real-time PCR assays to determine the total viral load and to identify the presence of one or more of 13 high risk HPV genotypes in the sample; b) second line assays to be applied to samples positives for: - 5 independent TaqMan Real-time PCR assays to determine the presence and the viral load of the most common oncogenic HPV types: HPV types: 16, 18, 31, 45, 33 group (including 33, 52, 58, 67 genotypes). - 6 independent SYBR Green I RT Real-time PCR assays to determine the presence in the sample of the oncogenic transcripts E6/E7 of HPV types 16, 18, 31, 33, 45, 58.
机译:鉴定和定量致癌HPV核酸的方法,包括:a)通过5种独立的SYBR Green I实时PCR分析法进行一线筛选,以确定总病毒载量并鉴定13种高危人群中的一种或多种样本中的HPV基因型; b)应用于阳性样品的二线检测:-5种独立的TaqMan实时PCR检测,以确定最常见的致癌HPV类型的存在和病毒载量:HPV类型:16,18,31,45,33组(包括33、52、58、67个基因型)。 -6个独立的SYBR Green I RT实时PCR分析法,用于确定样本中是否存在HPV类型16、18、31、33、45、58的致癌转录本E6 / E7。

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