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- Adam Mickiewicz University, Poznań
- Institute of Biochemistry and Biophysics Polish Academy of Sciences
- International Institute of Molecular and Cell Biology in Warsaw
- Nencki Institute of Experimental Biology
- ENSEMBLE3 Sp. z o. o.
- Institute of Bioorganic Chemistry Polish Academy of Sciences
- Institute of Physical Chemistry, Polish Academy of Sciences
- Lodz University of Technology
- Medical University of Gdańsk
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Field
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Time-Domain Spectroscopy, Hall measurements, Raman microscopy, device fabrication, Scanning Electron Microscopy, Instrument control in LabVIEW or python, synthesis of 2D materials, 2D materials
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; immunofluorescence and immunohistochemistry; proximity ligation assays; microscopy techniques (widefield, confocal, super-resolution STED, correlative light and electron microscopy, atomic force microscopy, multiplex
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sensitive fluorescent probes to identify, localise and quantitatively assess the activity of selected proteases in cancer cells, neutrophils, PBMCs and tissue samples. The use of advanced confocal microscopy
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; Skills: brain surgery and behavioral tests on rodents, or advanced image and data analysis; Experience in iDISCO brain clearing, light sheet microscopy and data analysis, miniendoscopes application in a
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Infrastructure? No Offer Description KEY WORDS: amyotrophic lateral sclerosis, frontotemporal dementia (ALS/FTD), pathogenesis of ALS/FTD, RNA-protein interactions, cryogenic electron microscopy
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). Experience with advanced microscopy techniques, such as confocal and super-resolution microscopy (preferred). Fluency in English, both written and spoken LanguagesENGLISHLevelExcellent Research FieldBiological
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(knowledge of time-resolved spectroscopy will be an additional asset); • Expertise in the study of morphology and structure of thin organic layers (AFM and scanning probe microscopy, electron microscopy
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for mitochondrial mRNA levels and degradation using a fluorescent microscopy-based approach. The proteins identified in this screening will be further characterized through various molecular, biochemical, and
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for mitochondrial mRNA levels and degradation using a fluorescent microscopy-based approach. The proteins identified in this screening will be further characterized through various molecular, biochemical, and
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-molecule TIRF microscopy, biochemical reconstitution, and fluorescent labeling, we will observe individual RNA molecules and degradosome complexes in action, capturing millisecond-scale dynamics that shape