终端(电信)
载体(分子生物学)
生物
病毒学
长终端重复
实时聚合酶链反应
遗传学
物理
血清型
基因
腺相关病毒
重组DNA
计算机科学
基因表达
电信
作者
Christine Aurnhammer,Maren Haase,Nadine Muether,Martin A Hausl,Christina Rauschhuber,Ingrid Huber,Hans Nitschko,Ulrich Busch,Andreas Sing,Anja Ehrhardt,Armin Baiker
出处
期刊:Human Gene Therapy
[Mary Ann Liebert]
日期:2011-06-06
卷期号:: 110805114044008-110805114044008
被引量:9
摘要
Abstract Viral vectors based on various naturally occurring adeno-associated virus (AAV) serotypes are among the most promising tools in human gene therapy. For the production of recombinant AAV (rAAV) vectors, researchers are focusing predominantly on cross-packaging an artificial AAV genome based on serotype 2 (AAV2) into capsids derived from other serotypes. Within the packaged genome the inverted terminal repeats (ITRs) are the only cis-acting viral elements required for rAAV vector generation and depict the lowest common denominator of all AAV2-derived vector genomes. Up to now, no quantitative PCR (qPCR) for the detection and quantification of AAV2 ITRs could be established because of their extensive secondary hairpin structure formation. Current qPCR-based methods are therefore targeting vector-encoded transgenes or regulatory elements. Herein we establish a molecular biological method that allows accurate and reproducible quantification of AAV2 genomes on the basis of an AAV2 ITR sequence-specific...
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