BrpHMA2 fused to the firefly LUC gene (BrpHMA2::LUC) was constructed in pGreenII 0800-LUC as a reporter, and BrpNACs or other AREBs were constructed in the pGreenII 62-SK vector as effectors. pGreenII 62-SK and pGreenII 0800-LUC vectors were used for transient expression assays in tobacco leaves. The reporter and effector were transiently expressed in tobacco leaves mediated by Agrobacterium GV3101 (pSoup). Agrobacterium-infected plants were cultivated under low irradiance for 24 hours and then transferred to light for an additional 2 days [45 (link)]. The LUC signal in the transfected leaves was detected with a CCD camera (Vilber Newton 7.0).
Transient expression assay for BrpHMA2::LUC in tobacco
BrpHMA2 fused to the firefly LUC gene (BrpHMA2::LUC) was constructed in pGreenII 0800-LUC as a reporter, and BrpNACs or other AREBs were constructed in the pGreenII 62-SK vector as effectors. pGreenII 62-SK and pGreenII 0800-LUC vectors were used for transient expression assays in tobacco leaves. The reporter and effector were transiently expressed in tobacco leaves mediated by Agrobacterium GV3101 (pSoup). Agrobacterium-infected plants were cultivated under low irradiance for 24 hours and then transferred to light for an additional 2 days [45 (link)]. The LUC signal in the transfected leaves was detected with a CCD camera (Vilber Newton 7.0).
Corresponding Organization : Shenzhen University
Other organizations : Jilin Academy of Traditional Chinese Medicine, South China Normal University, Zhaoqing University, Nanjing Agricultural University, University of California, Riverside
Variable analysis
- BrpHMA2::LUC reporter
- BrpNACs or other AREBs as effectors
- LUC signal in the transfected leaves
- PGreenII 62-SK vector
- PGreenII 0800-LUC vector
- Agrobacterium GV3101 (pSoup)
- Cultivation under low irradiance for 24 hours followed by 2 days of light
- Positive control: Not explicitly mentioned
- Negative control: Not explicitly mentioned
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