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fluorescent proteins, SNAP-tag labeling, and related cell-based imaging approaches. • Prepare samples for and perform experiments using super-resolution microscopy and single-molecule fluorescence imaging
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-resolution microscopy and/or single-molecule fluorescence imaging applied to biological problems in cells. • Proven experience in quantitative analysis of membrane protein organization, oligomeric states, or
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and tumor tissue) to determine their immune cell infiltration profiles 3D imaging analyses using fluorescence microscopy techniques (e.g., confocal laser scanning microscopy, light-sheet fluorescence
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HBIGS Heidelberg Biosciences International Graduate School | Heidelberg, Baden W rttemberg | Germany | 5 days ago
and temporal dynamics of phyB PBs relative to nucleosomes using live imaging (phyB and H2B fluorescent lines) and MINFLux super-resolution microscopy at the 10-50 nm scale (using SNAP-tagged phyB and
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responsible for: Analysis of murine tissue samples (heart and tumor tissue) to determine their immune cell infiltration profiles 3D imaging analyses using fluorescence microscopy techniques (e.g., confocal
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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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, cellular and molecular biology Animal handling, animal injections Tissue processing and staining Cell/tissue imaging techniques such as fluorescence and confocal microscopy Online Application Required
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emphasis on techniques used for optical imaging of the human retina. It centers on two-photon fluorescence ophthalmoscopy employing femtosecond laser sources. This technique offers new opportunities
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methodologies including in vivo calcium imaging, optogenetics, electrophysiology, and molecular approaches. The work will be conducted in an international and collaborative research environment, offering
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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