Cozzi Jean, Anegon Ignacio, Braun Valérie, Gross Anne-Catherine, Merrouche Christel, Cherifi Yacine
genOway SA, 69362, Lyon, France.
Methods Mol Biol. 2009;561:73-88. doi: 10.1007/978-1-60327-019-9_5.
In the absence of germ-line-competent ES cells in the rat, pronuclear microinjection remains an essential tool to generate transgenic rat models. However, DNA microinjection procedures first developed for mouse do not provide scientists with satisfying results when applied to rat. Here we describe optimized procedures for rat with a special focus on rat embryo production, in vitro incubation and culture, DNA pronuclear injection, and the transfer of embryos into foster females.
由于大鼠中缺乏具有种系能力的胚胎干细胞,原核显微注射仍然是生成转基因大鼠模型的重要工具。然而,最初为小鼠开发的DNA显微注射程序应用于大鼠时,无法为科学家提供令人满意的结果。在此,我们描述了针对大鼠的优化程序,特别关注大鼠胚胎的产生、体外孵育和培养、DNA原核注射以及将胚胎移植到代孕母鼠体内。