I am using the pBAD24 arabinose inducible system in Shigella to express a protein of interest. My goal is to maintain induction of this protein during intracellular plaque assays. These assays require my mammalian cells to be plated 2 days prior to infection, then 3 days to allow for visible plaque formation. Thus, I need my cells to be glucose free for at least 5-6 days during my assay. Since this construct is repressed in the presence of glucose, I will not get any expression of my protein in typical cell culture media, which contains high glucose. Is it possible to grow mammalian cells without glucose? 

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