Effect of Bcl-2 expression for BARF1 gene transfected into human gastric epithelial cells
Shuying Li
Abstract
Shuying Li
Abstract
Objective To investigate effect of Bcl-2 expression for BARF1 gene transfected into human gastric epithelial cells.Methods BARF1 gene carried by eukaryotic vector PIRES2-EGFP/BARF1 was transfected into human gastric epithelial cell GES-1,monoclonal was screened by G418.Bcl-2 was detected by Immunohistochemistry in each group(including non-transfected GES-1,transfected with empty vector GES-1 and BARF1 gene transfected GES-1).Results The human gastric epithelial cells of stable expression BARF1 gene was obtained.The expression of Bcl-2 was higher for the GES-1 cells of transfected BARF1 gene than those of untransfected GES-1 and transfected with empty vector GES-1.Conclusion The expression of Bcl-2 may be regulated in human gastric epithelial cells of BARF1 gene transfected.
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Objective To investigate effect of Bcl-2 expression for BARF1 gene transfected into human gastric epithelial cells.Methods BARF1 gene carried by eukaryotic vector PIRES2-EGFP/BARF1 was transfected into human gastric epithelial cell GES-1,monoclonal was screened by G418.Bcl-2 was detected by Immunohistochemistry in each group(including non-transfected GES-1,transfected with empty vector GES-1 and BARF1 gene transfected GES-1).Results The human gastric epithelial cells of stable expression BARF1 gene was obtained.The expression of Bcl-2 was higher for the GES-1 cells of transfected BARF1 gene than those of untransfected GES-1 and transfected with empty vector GES-1.Conclusion The expression of Bcl-2 may be regulated in human gastric epithelial cells of BARF1 gene transfected.
Key concepts: Transfection, Molecular biology, Gene, Immunohistochemistry, Expression vector, Gene expression, Biology, Cell