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Field
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thermophilic and mesophilic lignin hydrolyzing gene(s) in a single, multigene, or synthetic operon manners into plant expression plasmid vectors and using these constructed cassettes for developing/recovering
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, and Python to process vector and raster data for agronomic decision-making - Documented experience with producing educational communications and programming - Demonstrated ability to effectively
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, SciPy, etc., and traditional ML models such as support vector machines (SVMs) and Gradient Boosting Machines (GBM), as well as deep learning models (GNN, CNN, GCN, etc.) including LLMs. Being able
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plasmid vectors and protein-based approaches for transformation of Clostridial species Design, implement, and analyze repeatable experiments (in collaboration with the supervisor and other personnel
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behavioral experiments. Generation of lentiviral vector for in vivo or in vitro gene delivery; primary neuronal culture; human fibroblast and pluripotent stem cell culture. Compile and analyze data with
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technology, molecular and cellular biology including mammalian cell culture and assays of protein and nucleic acids, DNA sequencing, genetic engineering including production of viral vector delivery systems
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of plasmid and viral vectors, transfections, neutralization, western blotting, molecular cloning, ligand-binding, fluorescent imaging, structural characterization of membrane-bound or soluble viral proteins
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immunology, autoimmunity, neurodegenerative disease, molecular genetics/ biology, biochemistry, and virology. Responsibilities include management of all aspects of vector construction, cell culture, protein
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infrastructure leveraging Aurora’s storage system, DAOS, a Distributed Asynchronous Object Storage system, to meet the needs of AI-driven applications. Another goal would be to evaluate vector databases and
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University of California, Los Angeles | Los Angeles, California | United States | about 2 months ago
errors of immunity. Specifically, her research revolves around both viral vector mediated gene therapy and CRISPR/Cas9 mediated gene editing of HSC for the treatment of rare immune deficiencies. In