Sheng Wu Gong Cheng Xue Bao
January 2003
Recently, we have reported a new gfp gene isolated from Aequorea macrodactyla. The protein purified from expressed E. coli exhibited an excitation peak at 476 nm and an emission peak at 496 nm.
View Article and Find Full Text PDFAim: To improve the immunogenicity of receptor binding site of hepatitis B virus (HBV) on preS1 antigen using HBV core antigen as an immuno-carrier.
Methods: One to 6 tandem copies of HBV preS1 (21-47) fragment were inserted into HBcAg at the sites of aa 78 and 82, and expressed in E.coli.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi
July 2004
Aim: To express the fusion protein of enhanced green fluorescent protein (EGFP) with the light chain variable domain of the neutralizing monoclonal antibody MA18/7 (mAb) against hepatitis B virus in E.coli, and determine its bioactivity.
Methods: The EGFP gene was cloned into vector pTO-T7 to construct an expression vector.