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All quantitations were normalized to an endogeneous control GAPDH.
All quantitations were normalized to an endogenous β-actin control.
All quantitations were normalized versus endogenous GAPDH.
All quantitations were normalized to expression of mRNA for the human ribosomal protein L32.
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All quantitation was normalized to an endogenous control 18S gene (Assay ID: Hs99999901_s1).
All CAT quantitations were normalized to the protein concentration of the cell extract, as determined using the Coomasie Plus Protein Assay Reagent Kit (Pierce IL, USA). 3 × PPRE promoter activity was assessed with a dual-luciferase assay kit (Promega WI, USA).
Second, all datasets were normalized.
All values were normalized to GAPDH levels.
All values were normalized for histone H3.
All blots were normalized with β-tubulin.
All values were normalized against GAPDH expression.
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