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- W2363587206 abstract "Objective To construct the fibroblast growth factor 12(FGF21) expression vector. Methods FGF21 gene was cloned into shuttle plasmid p Ad-Track and then amplified in DH5 alpha bacteria. After restriction digestion with Pme I, it was transfected into the adenoviral backbone plasmid p Ad Easy-1 in BJ5183 competent bacteria by heat method. Ad-FGF21 was selected by kanamycin and identified by Pac I restriction enzyme, followed by amplified in DH5 alpha bacteria. Ad-FGF21 plasmid was linearized by Pac I and then transfected into 293 A cells. Results The shuttle vector p Ad-Track-FGF21 and recombinant adenovirus FGF21 expression vector were successfully constructed by gene sequencing, PCR and restriction enzyme digestion, respectively. The high-titer recombinant adenovirus was prepared by transfection with 293 A cells. ConclusionRecombinant adenovirus FGF21 expression vector can be successfully constructed using adenovirus vector system." @default.
- W2363587206 created "2016-06-24" @default.
- W2363587206 creator A5076190515 @default.
- W2363587206 date "2015-01-01" @default.
- W2363587206 modified "2023-09-25" @default.
- W2363587206 title "Construction and identification of FGF21 adenovirus expression vector" @default.
- W2363587206 hasPublicationYear "2015" @default.
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