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Field
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of Molecular & Human Genetics, Baylor College of Medicine. The laboratory uses cell culture, Drosophila and mouse genetics to identify and characterize genetic modifiers of human developmental disorders, in
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the experimental and bioinformatics analysis components—is essential. Proficiency in classical genomics techniques (RNA-seq, ChIP-seq, etc.) Proficiency in mouse ES cell culture and in vitro differentiation
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have research experience in the field of Chlamydia-host cell interactions, including practical experience in handling human cells cultures, conducting cell culture infection experiments with C
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outcomes. Perform molecular, cellular, and histological studies, which may include cell culture, tissue sectioning, immunohistochemical staining, microscopy, and related techniques. Collect, organize
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available in Yale’s Benefits Summary . Website https://shanshanliulab.com Contact Shanshan Liu, Ph.D., Assistant Professor, Department of Cell Biology, Yale School of Medicine; [email protected] Position
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stimulating multidisciplinary research environment focused on regulatory mechanisms that enable cells to retain their identity.We employ Drosophila and human cell culture models, genomics, genetics and
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MALDI-TOF characterization Cancer immunology Tumor immunology Vaccine development Immune checkpoint biology Mouse models of cancer Flow cytometry ELISA and antibody characterization Cell culture and
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University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | 2 days ago
skilled at mammalian cell culture; microfluidic device fabrication and implementation; designing experimental protocols; identifying the necessary resources; acquiring, processing, and interpreting data
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, biotechnology or a related field You have at least three years of experience with the development of cell-based assays that reflect a molecules mode of action. You are skilled in cell culture and fundamental
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resistance. This work will integrate spatial transcriptomics, advanced co-culture organoid assays, and in vivo models to decode the mechanisms underlying CAF-driven CRC evolution. Access to single cell RNA