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Transformants were shown to possess a similar 70 kb plasmid and resistance profile and were positive for blaCMY-2.

Fifteen of the seventeen transformants were shown to contain both the aphVIII gene and the g-luc gene.

Productions of solvents by E. coli transformants are shown in Figure1.

The Southern blot results for two randomly chosen transformants are shown in Figure 5B.

Seven double knockout strains out of the 32 transformants are shown in Fig.  5b.

The enzymatic activities of E1 in the leaf extracts of different primary (T0) rice transformants are shown in Figure 6A.

Examples for deviating phenotypes observed in gene-disruption library transformants are shown in Fig. 4b to 4E.

The PCR amplification confirmed the insertion of the hygromycin B resistance and crtS expression cassettes at the DHS3 locus in the heterozygous and homozygous transformants are shown in Figure  4.

In Figure 2, the 2-D gel electrophoresis images of the control transformant and the Yap1p-overexpressing transformant are shown.

This interaction was confirmed by plating these cells on more stringent plates (Fig. 3D, right panel; SD/-Ade/-His/-Trp/-Leu/+X-α-Gal/+AbA; one positive transformant was shown).

The data of a representative transformant are shown in Figure 2. The majority of the cells (88%) were flagellated and motile (Panel A) and strong signals corresponding to the unphosphorylated (lower band) and phosphorylated (upper band) forms of the RSP3-HA protein were detected in a Western blot using the anti-HA antibody (Panel B).