Effect of targeting NOS2 on gene expression of triple-negative breast cancer (metaplastic) SUM159 cell lines
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE234512
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To investigate the role of iNOS in tumor cell morphology and gene expression, we utilized CRISPR-Cas9 gene editing (NOS2 Double Nickase Plasmid, Santa Cruz) to knockout NOS2 in SUM159 cells. After puromycin selection, resistant clones were selected by immunoblotting for iNOS expression and nitrite/nitrate colorimetric assay. We then performed gene expression profiling analysis using data obtained from RNA-seq of parental SUM159 cells compared to NOS2KO SUM159 cells. RNA-seq of parental SUM159 cells compared to three clones of NOS2KO SUM159 cells.
创建时间：
2025-02-05
