Two-Photon microscopy (TPM) is an intravital imaging technique with deep tissue penetration, high three-dimensional resolution and low photobleaching. However, imaging speeds have traditionally been limited because images are generated by point scanning. Recently, Spectro-Temporal Laser Imaging by Diffractive Excitatio...
C. Stock, Gregory Berg, Matthea Thielking et al.· Frontiers in Photonics· 0 citations
Spectro-temporal laser imaging by diffractive excitation (SLIDE) enables two-photon microscopy (TPM) with 2D imaging rates in the kHz range and is capable of performing real-time volumetric imaging at video rates. However, the application of SLIDE microscopy is constrained by its available excitation wavelength. To dat...
S. Reinhards, T. Kutscher, K. Goodwin et al.· Optics Express· 0 citations
Fluorescence microscopy applications often require specialized instruments that are optimized for different experimental goals. Here, we present a reconfigurable microscopy module that integrates highly inclined swept tile (HIST) illumination for high-sensitivity single-molecule imaging and line-scanning confocal micro...
Christian Arthur, D. Milkie, Andrew J. Ulmer et al.· bioRxiv· 0 citations
Lattice light-sheet microscopy (LLSM) enables gentle, rapid, volumetric fluorescence imaging of living biological systems. The technique employs Bessel beam interference to produce a light-sheet which retains its thickness over a relatively large field-of-view compared to other light-sheets. In the decade since its com...
Helena L. E. Coker, David S. Corcoran· Journal of Microscopy· 0 citations
Super-resolution fluorescence microscopy has emerged as a powerful tool for investigating biological structures at the nanoscale, well beyond the diffraction limit of classical optical imaging. Among super-resolution techniques, single-molecule localization microscopy achieves this by sequentially imaging and localizin...
M. N. Alsamsam, A. Kopu̅stas, M. Tutkus· EPJ Web of Conferences· 0 citations
In vivo imaging of dynamic subcellular brain structures is key to understanding several phenomena in neuroscience. However, in the fruit fly, its implementation has been hindered by a trade-off among spatial resolution, speed, photobleaching, phototoxicity, and setup complexity required to access specific target regi...
Francisco J. Tassara, M. Barella, Tomás Sebastián Fernández Troncoso et al.· ACS Photonics· 0 citations
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