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Real-time quantitative RT-PCR amplification specificity. Amplified fragments obtained after qRT-PCR were separated by agarose gel electrophoresis. Amplification primers were designed for Actin (ACT), GAPDH, Cyclophilin (CYC), Elongation factor 1A (EF1A) and 2 (EF2), Ubiquitin (UBI), Ubiquitin extension protein (UBI 2), Tubulin (TUA), Eucaryotic Translation Initiation Factors 1A (ETIF1A), 3E (ETIF3E), 3H (ETIF3H), 4E (ETIF4E) and 5A (ETIF5A).
