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Generation of a cre recombinase-conditional Nos1ap over-expression transgenic mouse

机译:Cre重组酶条件性Nos1ap过表达转基因小鼠的产生

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摘要

Polymorphic non-coding variants at the NOS1AP locus have been associated with the common cardiac, metabolic and neurological traits and diseases. Although, in vitro gene targeting-based cellular and biochemical studies have shed some light on NOS1AP function in cardiac and neuronal tissue, to enhance our understanding of NOS1AP function in mammalian physiology and disease, we report the generation of cre recombinase-conditional Nos1ap over-expression transgenic mice (Nos1ap (Tg)). Conditional transgenic mice were generated by the pronuclear injection method and three independent, single-site, multiple copies integration event-based founder lines were selected. For heart-restricted over-expression, Nos1ap (Tg) mice were crossed with Mlc2v-cre and Nos1ap transcript over-expression was observed in left ventricles from Nos1ap (Tg); Mlc2v-cre F-1 mice. We believe that with the potential of conditional over-expression, Nos1ap (Tg) mice will be a useful resource in studying NOS1AP function in various tissues under physiological and disease states.
机译:NOS1AP基因座的多态性非编码变异与常见的心脏,代谢和神经系统性状和疾病有关。尽管基于体外基因靶向的细胞和生化研究为心脏和神经元组织中的NOS1AP功能提供了一些信息,但为了增强我们对NOS1AP在哺乳动物生理和疾病中功能的理解,我们报告了Cre重组酶条件性Nos1ap的产生。表达转基因小鼠(Nos1ap(Tg))。通过原核注射法产生条件转基因小鼠,并选择了三个独立的,单点,多拷贝整合事件的基础系。对于心脏受限的过表达,将Nos1ap(Tg)小鼠与Mlc2v-cre杂交,并在Nos1ap(Tg)的左心室中观察到Nos1ap转录本过表达。 Mlc2v-cre F-1小鼠。我们相信,具有条件性过度表达的潜力,Nos1ap(Tg)小鼠将成为研究生理和疾病状态下各种组织中NOS1AP功能的有用资源。

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