Published March 31, 2015 | Version v1
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Fig. 4 in Analysis of interactions between heterologously produced bHLH and MYB proteins that regulate anthocyanin biosynthesis: Quantitative interaction kinetics by Microscale Thermophoresis

  • 1. University of Stavanger, Centre for Organelle Research, Faculty of Science and Technology, N-4036 Stavanger, Norway

Description

Fig. 4. DFR expression in leaves of rosette stage plants wild type Ler, 35S:EGL3 in background gl3 egl3, and 35S:GL3 in background gl3 egl3. Expression changes are reported as fold increase compared to wild type Ler plants grown with 15 mM nitrate as calibrator, and ACT8 and UBQ genes were used as reference genes. Plants were grown for about 3 weeks with full nutrient medium under long-day conditions. Thereafter, the plants were grown with nutrient medium lacking nitrogen for 3 days before harvesting for qPCR analysis. Half of wild type Ler plants were kept to grow with 15 mM nitrate and used as calibrator. Each column represents the mean of three independent samples, and each sample contained 5 plants. The error bars indicate the standard error.

Notes

Published as part of Nemie-Feyissa, Dugassa, Heidari, Behzad, Blaise, Mickael & Lillo, Cathrine, 2015, Analysis of interactions between heterologously produced bHLH and MYB proteins that regulate anthocyanin biosynthesis: Quantitative interaction kinetics by Microscale Thermophoresis, pp. 21-26 in Phytochemistry 111 on page 24, DOI: 10.1016/j.phytochem.2015.01.004, http://zenodo.org/record/10487765

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Journal article: 10.1016/j.phytochem.2015.01.004 (DOI)
Journal article: urn:lsid:plazi.org:pub:0558FFC9FF8AFFE9FA6AC65FFFDFFFC6 (LSID)
Journal article: https://zenodo.org/record/10487765 (URL)