A new vector (pGZ1) was developed for bacterial phage display of antibody fragments using a transcriptional regulation element with tight control. The tet(p/o)-based phasmid exhibits fully suppressed scFv background synthesis in the absence of inducer and is independent of glucose as a catabolite repressor. The vector is shown to be a useful alternative to commonly used lac(p/o)-regulated systems.
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CITATION STYLE
Zahn, G., Skerra, A., & Höhne, W. (1999). Investigation of a tetracycline-regulated phage display system. Protein Engineering, 12(12), 1031–1034. https://doi.org/10.1093/protein/12.12.1031