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. 2013 Oct 22;45(23):1186–1192. doi: 10.1152/physiolgenomics.00087.2013

Fig. 1.

Fig. 1.

Agonist-dependent ERK and PKA responses in HEK293 cells that heterologously overexpress S49G389, G49G389, S49R389, and G49R389 haplotypes of the β1-adrenergic receptor (β1AR). Cell lysates from cells treated for 5 min with vehicle, isoproterenol (Iso, 1 μM), forskolin (Forsk, 10 μM), or EGF (100 ng/ml) were subjected to immunoblot analysis for pERK and pPKA substrate, as well as ERK protein (to verify equal protein loading) and β1AR (to track transgene expression) according to materials and methods. Results (means ± SE) from 3 separate experiments on separate culture preparations are quantified. *P < 0.05 vs. uninfected. #P < 0.05 vs. S49R389 or G49R389. S49R389 and G49R389 do not differ from each other.