生物
斑点印迹
基因组
重组DNA
载体(分子生物学)
病毒学
腺相关病毒
效价
实时聚合酶链反应
计算生物学
聚合酶链反应
遗传增强
分子生物学
DNA
基因
病毒
遗传学
作者
José Piedra,Maria Ontiveros,Susana Miravet,Cristina Penalva,Mercè Monfar,Miguel Chillón
标识
DOI:10.1089/hgtb.2014.120
摘要
Recombinant adeno-associated viruses (rAAVs) are promising vectors in preclinical and clinical assays for the treatment of diseases with gene therapy strategies. Recent technological advances in amplification and purification have allowed the production of highly purified rAAV vector preparations. Although quantitative polymerase chain reaction (qPCR) is the current method of choice for titrating rAAV genomes, it shows high variability. In this work, we report a rapid and robust rAAV titration method based on the quantitation of encapsidated DNA with the fluorescent dye PicoGreen®. This method allows detection from 3×1010 viral genome/ml up to 2.4×1013 viral genome/ml in a linear range. Contrasted with dot blot or qPCR, the PicoGreen-based assay has less intra- and interassay variability. Moreover, quantitation is rapid, does not require specific primers or probes, and is independent of the rAAV pseudotype analyzed. In summary, development of this universal rAAV-titering method may have substantive implications in rAAV technology.
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