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mammalian cell culture. Experience with expression (E. coli, yeast, and mammalian cells) and purification of proteins. Experience with Drosophila Genetics, Dissection, Immunostaining and Confocal Microscopy
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culture. Experience with expression (E. coli, yeast, and mammalian cells) and purification of proteins. Experience with Drosophila Genetics, Dissection, Immunostaining and Confocal Microscopy. Brief
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mammalian cell culture. Experience with expression (E. coli, yeast, and mammalian cells) and purification of proteins. Experience with Drosophila Genetics, Dissection, Immunostaining and Confocal Microscopy
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Other Position Time Status Full-Time Required Education Ph. D. in chemistry, biochemistry or closely related field. Required Related Experience Culture of E. coli, sterile technique, protein purification
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in the project funding the position: modular cloning of hydroxylases and CPR genes in Escherichia coli, expression of P450 and CPR in Saccharomyces cerevisiae, optimization of expression conditions
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working with diverse host organisms (e.g., E. coli, yeast, mammalian cells) is a significant plus. Deep expertise in advanced genome engineering tools (e.g., CRISPR/Cas systems, base editing, prime editing
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or suspension eukaryotic cell lines). Designing, establishing protocols and conducting recombinant protein expression experiments using eukaryotic or prokaryotic systems (HEK293, CHO, E. coli, etc.). Applying and
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the Escherichia coli model bacterium. More specifically, he/she will study the role of small proteins and small RNAs in controlling the activity of two-component systems, focusing on one of these systems involved
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secretion system of enteroaggregative E. coli, the type IV piliation machinery of Neisseria meningitidis, and rhoptry exocytosis signaling in Toxoplasma gondii. These protein complexes represent major targets