| Literature DB >> 27283422 |
Abstract
Recently we have explored and developed approaches imaging using confocal/two-photon microscopy, which enables simultaneous high-resolution assessment of specifically fluorescently marked cells in conjunction with structural components of the tissues visualized via harmonic generated signals. This approach uses commercially available confocal and two-photon laser microscope and automated user-interactive image analysis methods based on commercially available software packages allowing easy implementation in usual microscopy facilities.Keywords: Adipose tissue; Cell tracking; Fluorescent proteins; Lymph node; Multiphoton microscopy; Second harmonic generation; Third harmonic generation
Mesh:
Year: 2016 PMID: 27283422 DOI: 10.1007/978-1-4939-3721-9_11
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745