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performing biochemical assays. Conducting phage assays to test bacterial antiviral activity. Determining molecular structures using cryo-electron microscopy (cryo-EM). In addition, you will use bioinformatics
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: - Application of several light and electron microscopy techniques to study the infection strategies of archaeal viruses. - Perform protein interaction studies to unravel mechanisms by which viruses induce
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are looking for a PhD candidate for this project. Your responsibilities will include: Application of several light and electron microscopy techniques to study the infection strategies of archaeal viruses
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facilities hosted at UU’s Electron Microscopy Centre. Project description Recent advances in thermodynamic phase equilibrium modelling facilitate the prediction of metal budgets of crustal magmatic systems
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cell/molecular biology, biochemistry, chemical biology, or equivalent; Lab experience including: Mammalian cell culture, molecular biology (essential) CRISPR/Cas9, proteomics/lipidomics, microscopy
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genes and link it to changes of the spatial–temporal organization of specific polarity proteins through self-organization. Specifically, you will: Use high-throughput live-cell microscopy, quantitative
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-organization. Specifically, you will: Use high-throughput live-cell microscopy, quantitative image analysis, and set-up super-resolution microscopy to track these changes. Combine experimental data with
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, post-processing tools. Mechanical testing: tensile, hardness, nanoindentation, in-situ testing. Microstructural analysis: optical microscopy, SEM, EBSD, XRD. The expected start date is December 2025 (but
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assays (e.g., routine cell biology and biochemical measurements, ELISA and confocal microscopy) to unravel the underlying mechanisms of microplastics toxicity; we expect that you have to work with large
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culturing skills and exploit molecular assays (e.g., routine cell biology and biochemical measurements, ELISA and confocal microscopy) to unravel the underlying mechanisms of microplastics toxicity; we expect