首页> 外文期刊>Current Protocols in Mouse Biology >Tissue-Specific Regulation of Oncogene Expression Using Cre-Inducible ROSA26 Knock-In Transgenic Mice
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Tissue-Specific Regulation of Oncogene Expression Using Cre-Inducible ROSA26 Knock-In Transgenic Mice

机译:使用Cre可诱导的ROSA26敲入转基因小鼠的癌基因表达的组织特异性调节。

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摘要

Cre-inducible mouse models are often utilized for the spatial and temporal expression of oncogenes. With the wide number of Cre recombinase lines available, inducible transgenesis represents a tractable approach to achieve discrete oncogene expression. Here, we describe a protocol for targeting Cre-inducible genes to the ubiquitously expressed ROSA26 locus. Gene targeting provides several advantages over standard transgenic techniques, including a known site of integration and previously characterized pattern of expression. Historically, an inherent instability of ROSA26 targeting vectors has hampered the efficiency of developing ROSA26 knock-in lines. In this protocol, we provide individual steps for utilizing Gateway recombination for cloning as well as detailed instructions for screening targeted ES cell clones. By following this protocol, one can achieve germline transmission of a ROSA26 knock-in line within several months.
机译:Cre可诱导的小鼠模型通常用于癌基因的时空表达。利用大量可用的Cre重组酶系,诱导型转基因代表了实现离散癌基因表达的易处理方法。在这里,我们描述了一种针对Cre诱导型基因靶向无处不在表达的ROSA26基因座的协议。基因靶向提供了优于标准转基因技术的多个优势,包括已知的整合位点和先前表征的表达模式。从历史上看,ROSA26靶向载体的固有不稳定性已经阻碍了开发ROSA26敲入系的效率。在此协议中,我们提供了利用Gateway重组进行克隆的各个步骤,以及用于筛选目标ES细胞克隆的详细说明。通过遵循此协议,可以在几个月内实现ROSA26敲入系的种系传递。

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