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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Quantitation of human papillomavirus type 16 E6 oncogene sequences by real-time or quantitative PCR with EvaGreen
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Quantitation of human papillomavirus type 16 E6 oncogene sequences by real-time or quantitative PCR with EvaGreen

机译:使用EvaGreen实时或定量PCR定量人乳头瘤病毒16型E6癌基因序列

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Quantitation of E6 oncogene sequences of the human papillomavirus type 16 by real-time or quantitative PCR (qPCR) is used to determine the viral load, which correlates with the degree of the cervical neoplastic lesions. In the presence of EvaGreen, a new DNA intercalating fluorochrome, we obtained consistent and reproducible qPCR amplification curves and thermal denaturation profiles identical to those of the authentic E6-HPV16 (human papillomavirus 16) genome from the amplification products derived from a construct carrying the E6-HPV16 oncogene. E6-HPV16 quantitation in the presence of EvaGreen, therefore, is reproducible and specific and may be used to determine HPV16 viral load. (c) 2008 Elsevier Inc. All rights reserved.
机译:通过实时或定量PCR(qPCR)对人乳头瘤病毒16型的E6癌基因序列进行定量来确定病毒载量,该病毒载量与宫颈癌性病变的程度有关。在存在新的嵌入DNA的荧光染料EvaGreen的情况下,我们从带有E6的构建体得到的扩增产物中获得了与真实E6-HPV16(人乳头瘤病毒16)基因组相同的,可重复的qPCR扩增曲线和热变性图-HPV16癌基因。因此,在EvaGreen存在下进行E6-HPV16定量分析具有可重复性和特异性,可用于确定HPV16病毒载量。 (c)2008 Elsevier Inc.保留所有权利。

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