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The Technology
A a novel doxycycline-inducible vector (pRTST-1) was constructed. It consists of all the elements needed for tetracycline-inducible gene expression on one EBV-derived episomally replicating plasmid. A bicistronic expression cassette drives simultaneous expression of an optimized reverse transactivator and a tet-repressor-KRAB fusion protein acting as a repressor in eucaryotic cells. The vector is characterized by (i) its very low background activity in the absence, (ii) its high inducibility in the presence of doxycycline, and (iii) its graded response to increasing doxycycline or tetracycline concentrations. Tight regulation is achieved by binding of the repressor to the doxycycline-regulated bidirectional promoter in the absence of doxycycline, and combined relief of repression and binding of the reverse transactivator in the presence of doxycycline. In human B lymphoma lines stably transfected with pRTST-1, background of EGFP and luciferase expression was invariably very low, whereas inducibility varied among different clones and reached levels of 10.000 to 140.000-fold in individual single cells clones. Doxycycline-inducible plasmid pRTST-1 Source: Georg W. Bornkamm, GSF
Commercial Opportunity
The one-plasmid system pRTST-1 can be used for tightly controlled expression of genes in cells transiently or stably transfected with this episomal vector. There are several advantages of this plasmid system:
Patent situation
No patent was filed.
Further Reading
Bornkamm et al., manuscript in preparation
Contact: Dr. Hubert Müller T: +49 (0)89 318814-32 |
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