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Field
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microbiology and molecular biology. Ideally, the candidate will have experience with bacterial husbandry, cloning, genetics, microscopy/biological imaging and/or protein biochemistry. A strong publication record
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crosslinking/mass-spectrometry and single particle cryogenic electron microscopy on native or recombinant TZ complexes, you are expected to determine the molecular super-structure of TZ. You will monitor
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. Computational and bioinformatic skills. Experience in microscopy. Generation and analysis of mouse models. Handling of human samples. Molecular biology skills including CRISPR, cloning and qPCR. In vitro cell
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; have (or expect to have) a PhD in Molecular Biology or related field; research experience in one or more of the following protein purification, protein-nucleic acid biochemistry, cryo-electron
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ED data acquisition, analysis and use of in situ liquid and electrochemical TEM experiments, under the supervision of Professor Joke Hadermann. EMAT is one of the leading electron microscopy centers
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ED data acquisition, analysis and use of in situ liquid and electrochemical TEM experiments, under the supervision of Professor Joke Hadermann. EMAT is one of the leading electron microscopy centers
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ED data acquisition, analysis and use of in situ liquid and electrochemical TEM experiments, under the supervision of Professor Joke Hadermann. EMAT is one of the leading electron microscopy centers
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multiple microscopy techniques. The hired postdoctoral researcher will receive compensation based on the current NIH NRSA Kirschstein scale. In accordance with the University of Utah’s policies, he/she will
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force‑responsive probes, DNA‑based sensors, or advanced microscopy to understand mechanochemical signaling in cells. Operate and innovate with state‑of‑the‑art optical, fluorescence, and force
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Fluorescence microscopy, targeted gene editing using CRISPR-Cas9, programming skills and advanced image data analysis. Experience with research and development in an international team Informal inquiries about