Cryofixation yields outstanding ultrastructural preservation of cells for electron microscopy, but current methods disrupt live cell imaging. Here we demonstrate a microfluidic approach that enables cryofixation to be performed directly in the light microscope with millisecond time resolution and at atmospheric pressure. This will provide a link between imaging/stimulation of live cells and post-fixation optical, electron, or X-ray microscopy
Abstract Background Real-time monitoring of cellular responses to dynamic changes in their environme...
Sample fixation by vitrification is critical for the optimal structural preservation of biomolecules...
peer-reviewedMany proofs of concept have demonstrated the potential of microfluidics in cell biolog...
Cryofixation yields outstanding ultrastructural preservation of cells for electron microscopy, but c...
Cryofixation yields outstanding ultrastructural preservation of cells for electron microscopy, but c...
We present a microfluidic platform for studying structure-function relationships at the cellular lev...
We present a microfluidic platform for studying structure-function relationships at the cellular lev...
Light and electron microscopy are complementary methods to study biological systems at the cellular ...
Correlating live‐cell imaging with electron microscopy is among the most promising approaches to rel...
This paper highlights an innovative, low-cost rapid-prototyping method for generating microfluidic c...
The preservation of cells for electron microscopy by chemical fixation is a lengthy process, requiri...
Correlating complementary multiple scale images of the same object is a straightforward means to dec...
Three-dimensional (3D) structured illumination microscopy (SIM) allows imaging of fluorescently labe...
Rapid cryopreservation of biological specimens is the gold standard for visualizing cellular structu...
Studying biological structures with fine details does not only require a microscope with high resolu...
Abstract Background Real-time monitoring of cellular responses to dynamic changes in their environme...
Sample fixation by vitrification is critical for the optimal structural preservation of biomolecules...
peer-reviewedMany proofs of concept have demonstrated the potential of microfluidics in cell biolog...
Cryofixation yields outstanding ultrastructural preservation of cells for electron microscopy, but c...
Cryofixation yields outstanding ultrastructural preservation of cells for electron microscopy, but c...
We present a microfluidic platform for studying structure-function relationships at the cellular lev...
We present a microfluidic platform for studying structure-function relationships at the cellular lev...
Light and electron microscopy are complementary methods to study biological systems at the cellular ...
Correlating live‐cell imaging with electron microscopy is among the most promising approaches to rel...
This paper highlights an innovative, low-cost rapid-prototyping method for generating microfluidic c...
The preservation of cells for electron microscopy by chemical fixation is a lengthy process, requiri...
Correlating complementary multiple scale images of the same object is a straightforward means to dec...
Three-dimensional (3D) structured illumination microscopy (SIM) allows imaging of fluorescently labe...
Rapid cryopreservation of biological specimens is the gold standard for visualizing cellular structu...
Studying biological structures with fine details does not only require a microscope with high resolu...
Abstract Background Real-time monitoring of cellular responses to dynamic changes in their environme...
Sample fixation by vitrification is critical for the optimal structural preservation of biomolecules...
peer-reviewedMany proofs of concept have demonstrated the potential of microfluidics in cell biolog...