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Zhong Nan Da Xue Xue Bao Yi Xue Ban ; 32(6): 1047-50, 2007 Dec.
Article in Chinese | MEDLINE | ID: mdl-18182725

ABSTRACT

OBJECTIVE: To construct the plasmid of human vascular endothelial cell growth factor165 and green fluorescence protein report gene eukaryotic expression vector of fusion protein pEGFP /hVEGF165, and to detect its expression in vascular endothelial cells. METHODS: We amplified full-length of gene VEGF165 by PCR, cloned in direction in multiple clone sites of pEGFP-N1, constructed recombinant plasmid of pEGFP/hVEGF165. Through enzyme digestion, PCR, and sequencing analysis, we also performed liposome-mediated transfection of vascular endothelial cells of in vitro cultivation, and detected the expression of fusion protein pEGFP/hVEGF165 using fluorescence microscope, RT-PCR, and Western blot. RESULTS: Both gene VEGF165 and multiple clone site of pEGFP-N1 confirmed by PCR, enzyme digestion, and sequence analysis. EGFP/VEGF protein was expressed in vascular endothelial cells after pEGFP/VEGF165 recombinant plasmid transfected vascular endothelial cells. CONCLUSION: Fusion protein eukaryotic plasmid of report gene EGFP and VEGF165 is successfully constructed, and EGFP/VEGF can be expressed in vascular endothelial cells, which lays a foundation for the application of VEGF gene in treating ischemia vascular diseases.


Subject(s)
Genetic Vectors , Green Fluorescent Proteins/genetics , Recombinant Fusion Proteins/metabolism , Vascular Endothelial Growth Factor A/metabolism , Cells, Cultured , Endothelial Cells/metabolism , Gene Expression , Humans , Plasmids , RNA, Messenger , Recombinant Fusion Proteins/genetics , Transfection , Vascular Endothelial Growth Factor A/genetics
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