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首页> 外文期刊>Methods: A Companion to Methods in Enzymology >Genetic engineering of mammalian cells by direct delivery of FLP recombinase protein.
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Genetic engineering of mammalian cells by direct delivery of FLP recombinase protein.

机译:通过直接递送FLP重组酶蛋白对哺乳动物细胞进行基因工程。

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摘要

Protein transduction is based on the ability of certain peptides, designated as cell penetrating peptides (CPPs), to intracellularly deliver cargo molecules, such as peptides and proteins. In combination with site specific recombination, CPP-mediated delivery of recombinases enables a precise and highly efficient control of gene expression in cultured cells and mice. Herein, we provide detailed protocols for engineering and purification of a cell-permeant FLP recombinase protein. Two examples describe the use of cell permeant FLP for excising prespecified fragments from transgenes expressed in fibroblasts and mouse embryonic stem cells. A third example describes the combined use of cell-permeant Cre and FLP recombinases to reversibly induce transgenes in embryonic stem cells. We anticipate that the protocols described herein will be widely used for various genetic interventions addressing complex biological questions.
机译:蛋白质转导基于某些被称为细胞穿透肽(CPPs)的肽在细胞内递送货物分子(如肽和蛋白质)的能力。与位点特异性重组相结合,CPP介导的重组酶传递可精确,高效地控制培养细胞和小鼠中的基因表达。在此,我们提供了用于工程设计和纯化细胞渗透性FLP重组酶蛋白的详细协议。两个例子描述了使用细胞渗透性FLP从成纤维细胞和小鼠胚胎干细胞中表达的转基因中切除预定片段。第三个例子描述了结合使用细胞渗透性Cre和FLP重组酶可逆地诱导胚胎干细胞中的转基因。我们预期本文所述的方案将被广泛用于解决复杂生物学问题的各种遗传干预。

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