Fig. 1: Relative expression levels of VvSTS48 (VIT_16s0100g01200), VvSTS16 (VIT_16s0100g00920), VvSTS19 (VIT_16s0100g00750), and VvCHS (VIT_05s0136g00260) measured by quantitative reverse transcription-polymerase chain reaction (RT-qPCR). | Horticulture Research

Fig. 1: Relative expression levels of VvSTS48 (VIT_16s0100g01200), VvSTS16 (VIT_16s0100g00920), VvSTS19 (VIT_16s0100g00750), and VvCHS (VIT_05s0136g00260) measured by quantitative reverse transcription-polymerase chain reaction (RT-qPCR).

From: Biological and molecular interplay between two viruses and powdery and downy mildews in two grapevine cultivars

Fig. 1

Samples were collected before inoculation with P. viticola or E. necator (T0) and at the end of experiments (Tf). RT-qPCR signals were normalized to VvAct and VvUBI transcripts. NE_CTR, CH_CTR: virus-free plants; NE_GRSPaV, CH_GRSPaV: GRSPaV-infected plants; NE_GFLV, CH_GFLV: GFLV-infected plants. Data are presented as the mean ± standard deviation (SD) (n = 3). Lowercase letters denote significant differences attested by Tukey’s honestly significant difference (HSD) test (p ≤ 0.05)

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