| Literature DB >> 32421923 |
Jialin Wang1, Jia Zhang1, Luwei Wang1, Xinwei Gao1, Yonghong Shao1, Liwei Liu1, Zhigang Yang1, Wei Yan1, Junle Qu1.
Abstract
STED (stimulated emission depletion) microscopy is one of the most promising super-resolution fluorescence microscopies,due to its fast imaging and ultra-high resolution. In this paper, we present a dual-color STED microscope with a single laser source. Polarization beam splitters are used to separate the output from a supercontinuum laser source into four laser beams, including two excitation beams (488, 635 nm) and two depletion beams (592, 775 nm). These four laser beams are then used to build a low cost dual-color STED system to achieve a spatial resolution of 75 nm in cell samples.Entities:
Keywords: STED microscopy; cell imaging; dual-color imaging; super-resolution; supercontinuum laser
Mesh:
Year: 2020 PMID: 32421923 DOI: 10.1002/jbio.202000057
Source DB: PubMed Journal: J Biophotonics ISSN: 1864-063X Impact factor: 3.207