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. Author manuscript; available in PMC: 2010 Jan 1.
Published in final edited form as: Genomics. 2008 Oct 25;93(1):62–71. doi: 10.1016/j.ygeno.2008.09.002

Fig. 3.

Fig. 3

Activity of both MSRA promoters in D407, HEK 293 and SH-SY5Y and cell lines. Various constructs containing different areas of both MSRA promoters (D) were cloned into pGL4 luciferase reporter vector and transfected into different cell lines. A. Relative luciferase activity of both promoters in D407 RPE-derived cell line. B. HEK 293 kidney-derived cell line. C. SH-SY5Y neuroblastoma cell line. D. Constructs used (Table 1). The activity of promoter 1 is represented in dark grey and promoter 2 in light grey. All the results were normalized by renilla luciferase transfection control and related to the pGL4 empty vector. Data (Mean ± SD of three measurements) are representative of three or more independent experiments.