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not limited to bacterial sepsis, viral infections, and cancer. Candidate will perform in vitro and in vivo experiments and contribute to the laboratory research program. The candidate will organize
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bacterial origin. Where to apply Website https://emploi.cnrs.fr/Candidat/Offre/UMR8175-FLOGAZ0-008/Candidater.aspx Requirements Research FieldPharmacological sciencesEducation LevelPhD or equivalent Research
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Gottfried Wilhelm Leibniz Universität Hannover | Hannover, Niedersachsen | Germany | about 1 month ago
for a fully funded PhD position within the DFG Priority Programme SPP2389 https://tu-dresden.de/mn/biologie/allgemeine_mikrobiologie/spp2389 . International collaboration The PhD is embedded in a close
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, including the production of gene-edited (knockout) poultry using CRISPR/Cas9 technology and the development of poultry lines resistant to bacterial and viral infections. Duties and Responsibilities: (70
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biology techniques including, but not limited to, PCR, protein/DNA/RNA extraction and gel electrophoresis, bacterial transformation, imaging, cloning, gene-editing (such as CRISPR), small and large scale
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. Responsibilities include applying methods such as gene cloning, PCR, site-directed mutagenesis, protein expression, purification and characterization, bacterial and mammalian cell culture, ELISA, HIV virus titration
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information: https://monacklab.stanford.edu/publications This is a great position for someone interested in gaining broad research experience in microbiology, bacterial genetics and mouse models. The ideal
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techniques, such as DNA/RNA extractions, and polymerase chain reaction (PCR) to determine the presence, or absence of bacterial, protozoa, fungi, viruses, or other pathogenic microorganisms. Performs
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/RNA extractions, and PCR. Performs laboratory testing using scientific techniques, such as DNA/RNA extractions, and polymerase chain reaction (PCR) to determine the presence, or absence of bacterial
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of heterogeneity, and opportunities to modulate diet-derived microbiota-dependent metabolites (MDMs) for beneficial host signaling. We use computational methods and mass spectrometry to quantify bacterial