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. 2022 Jan 20;12:821281. doi: 10.3389/fgene.2021.821281

FIGURE 5.

FIGURE 5

(A) Confirmation of T0 transgenic Arabidopsis plants transformed with AhGLP17-1P (667 bp fragment). Eight hygromycin-resistant plants verified by PCR amplification with promoter-specific forward and GUS gene specific reverse primer. Arabidopsis Col-0 was used as –ve control, and Gateway LR constructs were used as + ve control for PCR verification. M shows 2 kb marker, (B) Quantitative expression of GUS gene driven by AhGLP17-1P in different tissues of transgenic Arabidopsis plants. Root expression was used as control to analyse the data.