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Light Sheet-based Fluorescence Microscopy of Living or Fixed and Stained Tribolium castaneum Embryos
Published on: April 28, 2017
Live-imaging fluorescent proteins in mouse embryos: multi-dimensional, multi-spectral perspectives.
Sonja Nowotschin1, Guy S Eakin, Anna-Katerina Hadjantonakis
1Developmental Biology Program, Sloan-Kettering Institute, New York, NY10065, USA.
Trends in Biotechnology
|April 3, 2009
Summary
Live imaging in developmental biology has been revolutionized by fluorescent proteins (FPs). Recent advances enable high-resolution, in situ observation of dynamic processes in mouse embryos.
Area of Science:
- Developmental Biology
- Cellular Imaging
- Molecular Interactions
Background:
- Microscopy is crucial for understanding cell specification and body plan development.
- The discovery of green fluorescent protein (GFP) and other fluorescent proteins (FPs) has transformed live-cell imaging.
- Advancements in imaging technology and FP spectral diversity allow high-resolution, in situ observation of dynamic processes.
Purpose of the Study:
- To review recent advances in live-imaging techniques for developmental biology.
- To highlight the application of these techniques in mouse embryology.
- To discuss the impact of fluorescent proteins on the field.
Main Methods:
- Utilizing advanced microscopy techniques.
- Employing genetically encoded fluorescent proteins (FPs).
- Live imaging of mouse embryos in situ.
Main Results:
- High-resolution imaging of dynamic cellular processes is now achievable.
- Mouse models offer significant genetic tractability for embryological studies.
- The integration of sophisticated imaging and FPs provides unprecedented insights.
Conclusions:
- Live imaging with FPs has revolutionized developmental biology research.
- The mouse is a key model organism for studying mammalian embryogenesis using these advanced techniques.
- Continued innovation in imaging and FPs promises further breakthroughs in understanding development.

