A, total RNA from rat islets as well as FACS-purified α- and β-cells was reverse transcribed into cDNA. PCR analysis was performed using specific primers against GABABR1a-d,f, GABABR1a,f, GABABR1c,f, GABABR1d and GABABR2 (+). In the negative control reaction (−) reverse transcriptase was omitted. Molecular standards are shown to the left and the right. B, multiplex RT-PCR on islets (isl) and purified α- and β-cell with specific primers against insulin and glucagon.