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Improved silencing vector co-expressing GFP and small hairpin RNA

机译:共表达GFP和小发夹RNA的改良沉默载体

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Small interfering RNA (siRNA) is a powerful tool for the specific silencing of gene expression. We developed an improved vector pG-SUPER, that co-expresses green fluorescent protein (GFP) and small hairpin RNA simultaneously to,facilitate analysis of silencing at the level of individual cells. As a test system, we analyzed lamin A/C knockdown in HeLa cells. The GFP signal was a reliable reporter (93%-98%) of strong knockdown (approximate 90%) over a wide range of GFP intensities. The GFP reporter made possible the application of fluorescent-activated cell sorting (FACS) to purify the knockdown cell population. Such Populations facilitated Western blotting analysis to determine depletion of the target protein. pG-SUPER was also applied to evaluate gene replacement by exogenous genes rendered refractory to siRNA by introducing silent mutations. Recovery of lamin A was linearly correlated to the expression level of the rescue gene. pG-SUPER will expand plasmid-based siRNA applications through the easy and reliable detection of knockdown and rescued cells.
机译:小干扰RNA(siRNA)是基因表达特异沉默的强大工具。我们开发了一种改良的载体pG-SUPER,可同时表达绿色荧光蛋白(GFP)和小发夹RNA,以促进单个细胞水平的沉默分析。作为测试系统,我们分析了HeLa细胞中的层状A / C敲低。 GFP信号是在很宽的GFP强度范围内强敲除(大约90%)的可靠报告者(93%-98%)。 GFP报告基因使荧光激活细胞分选(FACS)应用于纯化敲除细胞群成为可能。这样的种群促进了蛋白质印迹分析以确定靶蛋白的消耗。 pG-SUPER还被用于通过引入沉默突变来评估被siRNA抑制的外源基因对基因的替代。核纤层蛋白A的回收率与救援基因的表达水平线性相关。 pG-SUPER将通过简单可靠地检测敲除和拯救的细胞来扩展基于质粒的siRNA应用。

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