| Literature DB >> 27338568 |
Per Niklas Hedde1, Enrico Gratton1.
Abstract
Light sheet microscopy is a powerful technique for rapid, three-dimensional fluorescence imaging of large specimen such as drosophila and zebrafish embryos. Yet, beam divergence results in a loss of axial resolution at the periphery of the light sheet. Here, we demonstrate how an electrically tunable lens can be utilized to maintain the minimal, diffraction-limited thickness of the light sheet over a wide field of view (>600 µm) at high frame rates (40 fps). This mode of operation is necessary for the application of fluorescence fluctuation spectroscopy in images. Microsc. Res. Tech. 81:924-928, 2018.Entities:
Keywords: fluorescence fluctuation spectroscopy; fluorescence microscopy; light sheet microscopy
Mesh:
Year: 2016 PMID: 27338568 PMCID: PMC5479743 DOI: 10.1002/jemt.22707
Source DB: PubMed Journal: Microsc Res Tech ISSN: 1059-910X Impact factor: 2.769