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done to measure stiffness and burst strength as well as biological properties to investigate endothelial/smooth muscle cells attachment using fluorescent microscopy. The PDRA will be based at Hull
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, CRISPR/Cas9 gene editing, immunofluorescence, flow cytometry, and confocal microscopy. · Ability to design, execute, and interpret independent experiments. · Excellent written and oral communication skills
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will apply advanced electron microscopy techniques, including STEM to investigate the structure and behaviour of catalytic nanomaterials critical for green hydrogen and energy technologies. The candidate
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, and fluorescent microscopy. Experience in studying skin, hair follicle, skin cancer, or epithelial-mesenchymal interaction, and genetically engineered mouse models is a plus. The ideal candidate should
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medical environment. We have access to modern research infrastructure: equipment for cell and molecular biology, flowcytometry, advanced microscopy, genetic analysis, laboratories for working with viral
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lysosomal membrane damage in Parkinson’s disease. The selected candidate will apply cutting-edge technology, including high-end microscopy, unbiased screening strategies, organelle isolation and gene editing
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optoelectronic properties at multiple length scales using advanced local microscopy and characterization techniques (such as scanning probe–based approaches); Study of charge transport, recombination, 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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a strong preference given to candidates with experience in fluorophore synthesis experience in cell culture, biological assays and fluorescence microscopy proven ability to conduct research/scholarly
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electron microscopy (cryo-EM) to analyze native chromatin-associated complexes isolated from human cells or assembled in Xenopus (frog) egg extracts. By continuing to develop innovative approaches