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. 2016 Jun 3;11(6):e0154787. doi: 10.1371/journal.pone.0154787

Fig 1. Expression Patterns and Subcellular Localization of AtRAN1.

Fig 1

The results of qRT-PCR reveal. (A) Real-time PCR analysis the AtRAN1 gene expression pattern. (B) Subcellular localization of the vector control and AtRAN1 in transgenic Arabidopsis root cells. (C) Subcellular localization of the vector control, AtRAN1 in tobacco epidermal cells. DIC, differential interference contrast, referring to bright-field images of the cells. Time course analysis of AtRAN1, AtRAN2, and AtRAN3 expression during (D) cold acclimation (4°C). (E) Salt and (F) ABA treatment conditions. Arabidopsis seedlings were germinated and grown for 7 d before they were subjected to treatment. Actin2 was used as an internal control. The error bars show SD, and are from three independent replications. And the results were repeated three times. Asterisk (*) indicates significant difference (P < 0.05).