Table 1. Transformation efficiency of genes into Artemisia annua L. leaves using vacuum infiltration method (VIL), using syringe infiltration method (VSL) and hairy root using vacuum infiltration method .
| Sample | Blue Area to Total Area (%) | ||
| VIL | VSL | HR | |
| WT | 0 | 0 | 0 |
| AGL1 | 0 | 0 | 0 |
| Ads | 58.47±1.27 | 39.04±9.01 | 80.21±6.38 |
| ads-p19 | 97.13±1.2 | 92.55±1.39 | 96.00±0.26 |
| p19 | 98.25±0.54 | 89.82±1.08 | 99.42±0.55 |
| Co-T | 85.92±0.13 | 65.22±6.87 | 91.17±0.79 |
Note:WT = wild type leaves, Transformed leaves withAgrobacterium tumefaciens, AGL1 = without plasmid and gene, ads = single plasmid with ads gene, ads-p19 = single plasmid with ads and p19 genes, p19 = single plasmid with p19 gene, Co-T = double plasmids, one with ads, another with p19 gene.