We describe a customizable and cost-effective light sheet microscopy (LSM) platform for rapid three-dimensional imaging of protein dynamics in small model organisms. The system is designed for high acquisition speeds and enables extended time-lapse in vivo experiments when using fluorescently labeled specimens. We demonstrate the capability of the setup to monitor gene expression and protein localization during ageing and upon starvation stress in longitudinal studies in individual or small groups of adult Caenorhabditis elegans nematodes. The system is equipped to readily perform fluorescence recovery after photobleaching (FRAP), which allows monitoring protein recovery and distribution under low photobleaching conditions. Our imaging plat...
The nematode worm Caenorhabditis elegans has emerged as an important model organism in the study of ...
Light sheet-based fl uorescence microscopy (LSFM) is emerging as a powerful imaging technique for th...
Optimal image quality in light-sheet microscopy requires a perfect overlap between the illuminating ...
We describe a customizable and cost-effective light sheet microscopy (LSM) platform for rapid three-...
We describe a customizable and cost-effective light sheet microscopy (LSM) platform for rapid three-...
Visualizing protein dynamics is the key to a quantitative understanding of molecular mechanisms in b...
<p>Animals are maintained following standard procedures, collected and immobilized on agar pads, whi...
Fast and low phototoxic imaging techniques are pre-requisite to study the development of organisms i...
International audienceFast and low phototoxic imaging techniques are pre-requisite to study the deve...
Live observation of biological phenomena in the context of living organisms can provide important in...
Light sheet fluorescence microscopy enables fast, minimally phototoxic, three-dimensional imaging of...
Light sheet fluorescence microscopy enables fast, minimally phototoxic, three-dimensional imaging of...
The nematode worm Caenorhabditis elegans has emerged as an important model organism in the study of ...
Protein aggregation into insoluble inclusions is a hallmark of a variety of human diseases, many of ...
ABSTRACT Time-lapse fluorescence microscopy is an important tool for measuring in vivo gene dynamics...
The nematode worm Caenorhabditis elegans has emerged as an important model organism in the study of ...
Light sheet-based fl uorescence microscopy (LSFM) is emerging as a powerful imaging technique for th...
Optimal image quality in light-sheet microscopy requires a perfect overlap between the illuminating ...
We describe a customizable and cost-effective light sheet microscopy (LSM) platform for rapid three-...
We describe a customizable and cost-effective light sheet microscopy (LSM) platform for rapid three-...
Visualizing protein dynamics is the key to a quantitative understanding of molecular mechanisms in b...
<p>Animals are maintained following standard procedures, collected and immobilized on agar pads, whi...
Fast and low phototoxic imaging techniques are pre-requisite to study the development of organisms i...
International audienceFast and low phototoxic imaging techniques are pre-requisite to study the deve...
Live observation of biological phenomena in the context of living organisms can provide important in...
Light sheet fluorescence microscopy enables fast, minimally phototoxic, three-dimensional imaging of...
Light sheet fluorescence microscopy enables fast, minimally phototoxic, three-dimensional imaging of...
The nematode worm Caenorhabditis elegans has emerged as an important model organism in the study of ...
Protein aggregation into insoluble inclusions is a hallmark of a variety of human diseases, many of ...
ABSTRACT Time-lapse fluorescence microscopy is an important tool for measuring in vivo gene dynamics...
The nematode worm Caenorhabditis elegans has emerged as an important model organism in the study of ...
Light sheet-based fl uorescence microscopy (LSFM) is emerging as a powerful imaging technique for th...
Optimal image quality in light-sheet microscopy requires a perfect overlap between the illuminating ...