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. 2015 Nov 30;10(11):e0143892. doi: 10.1371/journal.pone.0143892

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© 2015 Xiang et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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Fig 5 — P53 and its promoter supplied with the kit were used as a positive control to verify the stability of these assays. The auto-activity of CmDFR promoter bait stain was tested on SD media lacking Ura in presence of AbA. CmbHLH1, CmbHLH2 and CmMYB6 were fused into pGADT7 (AD) and transformed separately into the bait stain. The binding was screened on SD media lacking Leu in presence of AbA¹⁷⁵.