Figure 1From: Selection of internal control genes for quantitative real-time RT-PCR studies during tomato development processPerformance of the amplification primers. Amplicons obtained by real-time PCR using cDNA (odd numbers) or gDNA (even numbers) as template, separated by agarose gel electrophoresis. Amplification primers were targeted to GAPDH (1–2), EFα1 (3–4), TBP (5–6), RPL8 (7–8), APT (9–10), DNAJ (11–12), TUA (13–14), TIP41 (15–16), SAND (17–18), CAC (19–20) and Expressed (21–22) tomato genes.Back to article page