绿色荧光蛋白
单元格排序
生物
分子生物学
Cre重组酶
基因敲除
细胞生物学
细胞
黄色荧光蛋白
移植
转基因
报告基因
基因
转基因小鼠
流式细胞术
遗传学
基因表达
外科
医学
作者
Mandar D. Muzumdar,Bosiljka Tasic,Kazunari Miyamichi,Ling Li,Liqun Luo
出处
期刊:Genesis
[Wiley]
日期:2007-09-01
卷期号:45 (9): 593-605
被引量:3355
摘要
Abstract The Cre/loxP system has been used extensively for conditional mutagenesis in mice. Reporters of Cre activity are important for defining the spatial and temporal extent of Cre‐mediated recombination. Here we describe mT/mG , a double‐fluorescent Cre reporter mouse that expresses membrane‐targeted tandem dimer Tomato (mT) prior to Cre‐mediated excision and membrane‐targeted green fluorescent protein (mG) after excision. We show that reporter expression is nearly ubiquitous, allowing visualization of fluorescent markers in live and fixed samples of all tissues examined. We further demonstrate that mG labeling is Cre‐dependent, complementary to mT at single cell resolution, and distinguishable by fluorescence‐activated cell sorting. Both membrane‐targeted markers outline cell morphology, highlight membrane structures, and permit visualization of fine cellular processes. In addition to serving as a global Cre reporter, the mT/mG mouse may also be used as a tool for lineage tracing, transplantation studies, and analysis of cell morphology in vivo. genesis 45:593–605, 2007. © 2007 Wiley‐Liss, Inc.
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