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at the nanoscale would enable accurate, label-free sensing in complex biomedical samples, thus transforming current approaches. To give a few examples, molecularly resolved nanoscopy would allow us to quantify drug
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manipulation of the host during infection. You will use co-immunoprecipitation to verify predicted protein-protein interactions and establish enzymatic assays and activity-based labelling to demonstrate
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microbiomes. Within this focus, the research group has a strong program in the synthesis and application of chemical probes in complex biological systems and measurements of probe labeling by LC-MS based
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laboratory at the School of Cardiovascular and Metabolic Medicine & Sciences at King's College London. The postholder will be part of a vibrant multi-disciplinary research group operating across different
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-cell interaction proteomics by proximity labeling, subcellular localization by spatial proteomics and fluorescence microscopy, and protein structure prediction by artificial intelligence and crosslinking
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physics knowledge into DL model design and training, these models outperform traditional methods even without labeled training data (https://www.nature.com/articles/s41524-022-00803-w ). Application spaces
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University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | 27 days ago
Scholar Position Title Post-Doc Research Associate - Cohen Vacancy ID PDS004493 Full-time/Part-time Full-Time Temporary Hours per week 40 FTE 1 Work Location Chapel Hill, NC Position Location North Carolina
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Apply now The Institute for History at the University of Leiden invites applications for: 1 Postdoc Position (0,8 fte): ‘Imperial Monetary Flows’ The postdoc will become part of the OCW
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, ICP), molecular biological (QPCR, metagenomics, transcriptomics) as well as stable isotopic cell-labelling techniques (NanoSIMS, GC-IRMS-PLFA), flowcytometry). The experiments carried out will be
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immune recognition. This position is funded by Wellcome as part of a broader effort to understand how T cells process information following contact with antigen-presenting cells at the nanoscale, with a