Nucleic acid molecule, corresponding vector, cell for stable co-expression of GFP-Flag-FXR and preparation method
A gfp-flag-fxr, nucleic acid molecule technology, applied in the field of cell engineering, can solve problems such as limited significance, large differences in zebrafish, and inability to study the downstream regulatory network of FXR, so as to improve the operation efficiency and expand the scope of research.
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[0029] The following will clearly and completely describe the technical solutions in the embodiments of the present invention with reference to the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are some of the embodiments of the present invention, but not all of them. Based on the embodiments of the present invention, all other embodiments obtained by persons of ordinary skill in the art without making creative efforts belong to the protection scope of the present invention.
[0030] 1. Preparation of target DNA fragment and vector
[0031] Use EcoR I and BamH I to double-digest plasmids pLVX-mCMV-ZsGreen-PGK-Puro and pUC57-pig FXR-Flag, and the restriction system is as follows:
[0032] (1) System 1:
[0033]
[0034] (2) System 2:
[0035]
[0036]
[0037] After the digestion is completed, the recovered and purified target fragment pig FXR-FLag (EcoRI / BamHI) is connected with the recovered and purified vec...
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