Therefore, we constructed a human LTIP gene promoter reporter gene plasmid, and then with the FXR eukaryotic expression vector transiently co-transfected into HepG2 cells, detection of reporter gene activity.

That is why we built a person start sub district report LTIP gene recombination of genes, and then with the tablets FXR eukaryotic express carriers instantaneous a total HepG dye into 2 cells, detection report genetic biologically active.

Therefore we constructed the human LTIP gene to start the sub-area report gene recombination material particle, then really nuclear expressed the carrier instant altogether extension with FXR to dye into the HepG2 cell, the examination reports the gene activeness.

So we built the human LTIP gene promoter reporter gene recombinant plasmid and eukaryotic expression vector and FXR in HepG2 cells transfected by instantaneous total, detection of reporter gene activity.

So we built the human LTIP gene promoter reporter gene recombinant plasmid and eukaryotic expression vector and FXR in HepG2 cells transfected by instantaneous total, detection of reporter gene activity.