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. Author manuscript; available in PMC: 2013 Dec 1.
Published in final edited form as: J Mol Endocrinol. 2013 Apr 23;50(3):361–374. doi: 10.1530/JME-12-0154

Figure 1.

Figure 1

CAT activity of rat AT1R reporter gene constructs in 25 μM 13cRA. CAT activity for serially deleted promoter fragments in pCAT vector was determined. (A) Schematic representation of the pCAT reporter expression vector containing serially deleted 5′ promoter region of the rat AT1R gene. (B) Solid bars represent the CAT activity of control plasmids, the value set automatically at 100% activity relative to β-galactosidase co-transfection control, patterned bars represent the comparative CAT activity in 25 μM 13cRA treated cells. Data are expressed as mean ± SEM, **p<0.01, n=3.