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Fig. 8 | Journal of Biological Engineering

Fig. 8

From: CRISPR/Cas9 mediated T7 RNA polymerase gene knock-in in E. coli BW25113 makes T7 expression system work efficiently

Fig. 8

Characterization of T7 RNAP promoter variants: Relative activity of promoter variants. Promoter variants were identified by referring to the base in the non-template strand of the DNA (e.g., a -17 A promoter). The height of each bar indicates the activity of each promoter relative to that of the consensus promoter (data are from Table 5). All experiments were performed in triplicates

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