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. 2018 Sep 4;25(6):597–617. doi: 10.1093/dnares/dsy028

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© The Author(s) 2018. Published by Oxford University Press on behalf of Kazusa DNA Research Institute.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 5. — Quantitative RT-PCR validation of expression of terpene synthase genes selected from the DGE analysis in S. guaranitica. Total RNAs were extracted from old leaves, young leaves, stem, flower, bud flower and root samples and the expression of SgGPPS, SgFPPS, SgHUMS, SgNEOD-1, SgNEOD-2, SgNEOD-3, SgTPS-1, SgTPS-3, SgTPS-6, SgLINS-1, SgLINS-2, SgGLNS, SgGERIS, SgTPS-V and SgFARD genes were analysed using quantitative real-time. SgACTIN was used as the internal reference. The values are means ± SE of three biological replicates.