| Literature DB >> 21886258 |
Marco Dal Maschio1, Angela Michela De Stasi, Fabio Benfenati, Tommaso Fellin.
Abstract
The acquisition of high-resolution images in three dimensions is of utmost importance for the morphological and functional investigation of biological tissues. Here, we present a laser scanning two-photon microscope with remote and motionless control of the focus position. The movement of the excitation spot along the propagation direction is achieved by shaping the laser wavefront with a spatial light modulator. Depending on the optical properties of the objective in use, this approach allows z movements in a range of tens to hundreds of micrometers with small changes of the point spread function. We applied this technique for the three-dimensional (3D) imaging of fluorescent cells in the mouse neocortex in vivo. The presented system bypasses the limitations of microscopes based on moving objectives, enabling high-resolution inertia-free 3D imaging.Entities:
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Year: 2011 PMID: 21886258 DOI: 10.1364/OL.36.003503
Source DB: PubMed Journal: Opt Lett ISSN: 0146-9592 Impact factor: 3.776