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. 2022 Nov 24;13(1):342–354. doi: 10.1080/21645698.2022.2141014

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© 2022 The Author(s). Published with license by Taylor & Francis Group, LLC.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 1. — T-DNA of pCAMBIA1302 and pCAMBIA2301 vectors used for transformation. (a) T-DNA region of pCAMBIA1302 harboring GFP reporter and hygromycin resistance genes (b) T-DNA region of pCAMBIA2301 harboring GUS reporter and kanamycin resistance genes. LB; left border, CaMV poly (A) signal; cauliflower mosaic virus polyadenylation signal, HygR; Resistance to hygromycin; NeoR/KanR; Resistance to Kanamycin, 35SP; 35S promoter, lacP; lac promoter, lacO; lac operon, MCS; multiple cloning sites, NOS T; Nopaline synthase terminator, RB; right border.