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neurons. Using a combination of high resolution live cell fluorescent imaging, electrochemistry and patch clamp electrophysiology, we recently discovered that activation of GLP-1Rs promotes the formation
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equivalencies: https://hr.uky.edu/employment/working-uk/equivalencies Required Related Experience No experience required. Required License/Registration/Certification Certification Physical Requirements Regularly
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Investigating how DNA damage responses combat infections by the typhoid pathogen Salmonella enterica
manipulation by intracellular Salmonella will be studied using fluorescent microscopes. Mass spectrometry will be exploited to identify DNA damage-associated antimicrobial pathways and provide a springboard for
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website for more information about our research interests: https://krupina.lab.uiowa.edu This position is designed for individuals who: • Seek training, experience, and mentoring in a research setting
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development and operation. More information can be found at: https://ppdo.ucsc.edu/physical-plant/building-utilities-and-fleet-services/ JOB SUMMARY Under the supervision and direction of the Electric Shop
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vitro reconstitution of recombinant membrane protein complexes and their biochemical and spectroscopic characterization (e.g., fluorescence and absorption spectroscopy). Isolation of membrane proteins
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biology and to perform the following duties and responsibilities under supervision: a variety of cellular a molecular assays in muscle biology and cancer biology to potentially include fluorescence
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secretion from chromaffin cells. Using a combination of patch clamp electrophysiology and live cell fluorescent imaging the interactions between heterotrimeric G protein subunits, their effectors and the
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Description We invite applications for a fully funded PhD position within the DFG Priority Programme SPP2389. https://tu-dresden.de/mn/biologie/allgemeine_mikrobiologie/spp2389?set_language=en
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in the laboratory (NT training in polymeric pillars, NT training in cryo-EM grid, protein purification, preparation of simple membrane molds, etc.) 4. Fluorescence and cryo-EM data acquisition on Dyn2