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. 2004 Jun 1;142(4):709–718. doi: 10.1038/sj.bjp.0705841

Figure 6.

Figure 6

Agarose-gel electrophoresis showing PCR products obtained when using specific primers for selected α1- and β-subunits of voltage-dependent Ca2+ channels and cDNA from mesenteric arterioles. The CaV2.1-P and CaV2.1-Q are alternative splice variants of the same gene and corresponds to the P-type and Q-type α1-subunits, respectively. CaV3.1-T corresponds to the α1G-subunit of T-type channels. β-2 (cardiac), β-3 (smooth muscle), and β-B (β1b, neuronal) are known β-subunits of high-voltage-activated Ca2+ channels. Specific primer for β-actin was also included in the reactions. Pooled cDNA from mesenteric arterioles in each of two rats were used (Prep 1, Prep 2). Appropriate controls are shown in which cDNA was omitted (neg. control) or 50 ng template cDNA isolated from various rat organs (cerebral cortex, left cardiac ventricle, or renal inner medulla) was included in the PCR (pos. control).