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Chapters
- 00:05Title
- 00:52Recombinatorial Cloning to Generate Ready-for-injection Clones
- 02:23Hydrodynamic Tail Vein Injection
- 04:22Induction of Transfected CreER with Tamoxifen
- 05:33Induction of Tetracycline-dependent Gene or shRNA Expression
- 06:35Preparation of Mouse Liver for Analysis by Immunostaining
- 07:30Results: Constitutive and Inducible Gene Expression in the Liver Following HTVI
- 08:47Conclusion
Hydrodynamic tail vein injection of transposon-based integration vectors enables stable transfection of murine hepatocytes in vivo. Here, we present a practical protocol for transfection systems that enables the long-term constitutive expression of a single transgene or combined constitutive and doxycycline-inducible expression of a transgene or miR-shRNA in the liver.
