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investigations. At the subcellular scale, laser scanning confocal fluorescence microscopy (CLSM) and spectral fluorescence lifetime imaging microscopy (spectral FLIM) will enable spatial mapping
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fluorescence (XRF) and optical reflectance and fluorescence imaging (hyperspectral/multispectral). The primary objective is multimodal unmixing, i.e., estimating pigment abundances at each location under scarce
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To address these challenges, the PRICELESS project aims to perform simultaneous measurements of flow velocity and Planar Laser-induced Fluorescence (PLIF) on OH and NO molecules at high repetition rate up to
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