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ClearSee: a rapid optical clearing reagent for whole-plant fluorescence imaging
Author(s) -
Daisuke Kurihara,
Yoko Mizuta,
Yoshikatsu Sato,
Tetsuya Higashiyama
Publication year - 2015
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.127613
Subject(s) - autofluorescence , biology , fluorescence , fluorescence lifetime imaging microscopy , molecular imaging , confocal microscopy , plant cell , microscopy , gene expression , computational biology , biophysics , gene , microbiology and biotechnology , biochemistry , optics , physics , in vivo
Imaging techniques for visualizing and analyzing precise morphology and gene expression patterns are essential for understanding biological processes during development in all organisms. With the aid of chemical screening, we developed a clearing method using chemical solutions, termed ClearSee, for deep imaging of morphology and gene expression in plant tissues. ClearSee rapidly diminishes chlorophyll autofluorescence while maintaining fluorescent protein stability. By adjusting the refractive index mismatch, whole-organ and whole-plant imaging can be performed by both confocal and two-photon excitation microscopy in ClearSee-treated samples. Moreover, ClearSee is applicable to multicolor imaging of fluorescent proteins to allow structural analysis of multiple gene expression. Given that ClearSee is compatible with staining by chemical dyes, the technique is useful for deep imaging in conjunction with genetic markers and for plant species not amenable to transgenic approaches. This method is useful for whole imaging for intact morphology and will help to accelerate the discovery of new phenomena in plant biological research.

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