This protocol is useful for determining changes in NF-kappa-B activation in cells expressing an NF-kappa-B luciferase reporter. The main advantage of this technique is it allows for a high-throughput screen of factors or conditions that lead to ch
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Here, we present a protocol to quickly and easily measure nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) activation in cell lines expressing NF-κB::luciferase reporter constructs, via measurements of luminescence in the cell lysate. Additionally, gene expression is determined via RT-qPCR isolated from cells infected with Salmonella Typhimurium.