Solving the focal shift problem in spatiotemporal focusing nonlinear microsocpy
POSTER
Abstract
Fluorescence imaging deep into mouse lung and snail demonstrates a doughty nonlinear microscopy with wide field of view, high contrast, fast acquisition-rate and near diffraction-limited axial resolution based on an ordinary ultrafast oscillator and spatiotemporal focusing nonlinear microscopy design. The key idea is that focal shift matching promotes near-diffraction-limited axial fluorescence optical sectioning for both low and high NA objectives without laser extra-cavity alteration.
Authors
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Kai Lou
IBS Center for soft and living matter
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Francois Amblard
IBS Center for soft and living matter
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Bo Wang
Departments of Bioengineering, Stanford University
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Steve Granick
IBS Center for Soft and Living Matter, IBS Center for soft and living matter