Live-imaging fluorescent proteins in mouse embryos: multi-dimensional, multi-spectral perspectives

被引:36
作者
Nowotschin, Sonja [1 ]
Eakin, Guy S. [1 ]
Hadjantonakis, Anna-Katerina [1 ]
机构
[1] Sloan Kettering Inst, Dev Biol Program, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
TRANSGENIC ZEBRAFISH EMBRYOS; IN-VIVO; MONOMERIC RED; STEM-CELLS; BIOLOGICAL APPLICATIONS; PHOTOACTIVATABLE GFP; GENE-EXPRESSION; QUANTUM DOTS; LIVING CELLS; GREEN;
D O I
10.1016/j.tibtech.2009.02.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Microscopy has always been an obligate tool in the field of developmental biology, a goal of which is to elucidate the essential cellular and molecular interactions that coordinate the specification of different cell types and the establishment of body plans. The 2008 Nobel Prize in chemistry was awarded 'for the discovery and development of the green fluorescent protein, GFP' in recognition that the discovery of genetically encoded fluorescent proteins (FPs) has spearheaded a revolution in applications for imaging of live cells. With the development of more-sophisticated imaging technology and availability of FPs with different spectral characteristics, dynamic processes can now be live-imaged at high resolution in situ in embryos. Here, we review some recent advances in this rapidly evolving field as applied to live-imaging capabilities in the mouse, the most genetically tractable mammalian model organism for embryologists.
引用
收藏
页码:266 / 276
页数:11
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