| Literature DB >> 29675298 |
Keisuke Toda1,2, Keisuke Isobe1,3, Kana Namiki4, Hiroyuki Kawano4, Atsushi Miyawaki1,4, Katsumi Midorikawa1,2.
Abstract
Super-resolution microscopy has become a powerful tool for biological research. However, its spatial resolution and imaging depth are limited, largely due to background light. Interferometric temporal focusing (ITF) microscopy, which combines structured illumination microscopy and three-photon excitation fluorescence microscopy, can overcome these limitations. Here, we demonstrate ITF microscopy using three-photon excitation fluorescence, which has a spatial resolution of 106 nm at an imaging depth of 100 µm with an excitation wavelength of 1060 nm.Keywords: (100.6640) Superresolution; (180.4315) Nonlinear microscopy; (180.6900) Three-dimensional microscopy
Year: 2018 PMID: 29675298 PMCID: PMC5905902 DOI: 10.1364/BOE.9.001510
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732