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reproducible sample preparation method for cryogenic electron microscopy (cryo-EM). You will fabricate microfluidic mechanical probes with phase guides, develop controlled dispensing of femto-liter volume
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: collaborate with the group of Dr Arnold Boersma at the Bijvoet Centre to develop novel sensors for measuring macromolecular crowding in C. elegans; use advanced fluorescence microscopy techniques, complemented
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of larval zebrafish. Data analysis: analyze whole‑brain calcium imaging recordings. Spatially resolved molecular methods: apply expansion microscopy (ExM) adapted for spatial transcriptomics to identify
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sensors for measuring macromolecular crowding in C. elegans; use advanced fluorescence microscopy techniques, complemented by molecular biology and biochemical methods; be an active member of an open and
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droplets; use super-resolution microscopy to investigate the molecular arrangement on the surface of milk fat globules and plant lipid droplets; develop chemical analytical tools (NMR, HPLC) to track
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PhD Development of a Low-Voltage Multi-Beam SEM for High-Throughput Imaging | TU Delft Job description Scanning Electron Microscopy (SEM) plays a central role in today’s nanoscale imaging across
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-chemical mapping to unravel the structure-function properties of single milk fat globules and plant lipid droplets; use super-resolution microscopy to investigate the molecular arrangement on the surface
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Development of a Low-Voltage Multi-Beam SEM for High-Throughput Imaging | TU Delft Job description Scanning Electron Microscopy (SEM) plays a central role in today’s nanoscale imaging across both science and
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development of operando and in-situ (time-resolved) spectroscopy and microscopy techniques to develop structure-performance relationships and understand, for example, the function and deactivation of solid
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microscopy (ExM) adapted for spatial transcriptomics to identify neuronal subpopulations underlying observed responses. Anatomical characterization: use transgenic lines to uncover morphological and