LXR stimulates a metabolic switch and reveals cholesterol homeostasis as a statin-target against Tasmanian Devil Facial Tumor Disease
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This is raw data related to the manuscript "LXR stimulates a metabolic switch and reveals cholesterol homeostasis as a statin-target against Tasmanian Devil Facial Tumor Disease"
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DFTD4 cells were lysed in cold RIPA buffer containing protease (Merck Pty Ltd, Kilsyth, Australia) and phosphatase (Roche Diagnostics, Castle Hill, Australia) inhibitors and stored at −20°C. Protein concentrations were determined using a Pierce BCA Protein assay kit (Thermo Fisher Scientific). Samples were subjected to SDS-PAGE and blotted according to standard procedures. In brief, 10 μg of protein was loaded per lane. Antibodies used for western blots are Phosphorylated AKT Threonine-308, Phosphorylated AKT Serine-473 and Total AKT (Cell signalling) and HRP-secondary antibodies (Sigma). Protein signals were visualized using enhanced chemiluminescence (Pierce™ ECL Western Blotting Substrate).