According to the BSE immunohistochemistry established by our lab, BSE positive sections and scrapie positive sections were firstly digested by proteinase K, then they were reacted with monoclonal antibody 4C11 and 6H4 as primary antibody.

Preparation and identification of monoclonal antibody against ginsenoside Rb1;

Development of monoclonal antibody against Fumonisin B_1 and ELISA-kit of quantitative analysis for Fumonisin B_1;

Determination of fipronil in water by ELISA based on monoclonal antibody;

Production and identification of monoclonal antibodies to chCD25;

Production and identification of monoclonal antibodies against proteinase activated receptor-1;

Expression and purification of recombinant nucleocapsid protein of SARS Coronavirus and preparation of its monoclonal antibodies;

Development and Characterization of MAb against Haemagglutinin of Highly Pathogenic H5 Avian Influenza Virus;

Preparation and characterization of non-agglutinating mAbs against membrane antigen on human erythrocytes;

Studies on the antithrombotic effects of anti-platelet mAb SZ-21 F(ab′)_2 fragment;

Observation to the stability of the McAb against the interior antigen of influenza A virus;

Preparation and Characterization of McAb against SARS-associated Coronavirus;

Establishment of Hybridoma Cell Secreting McAb Against DNA and Characterization of The Secreted McAb;

Application of monoclone antibody against Edwarsiella tarda;

Preparation of Monoclone Antibody (McAb) Against GST Tag Protein and Its Activity Identification;

A mouse-human 6C6 chimeric antibody gene, which is a linkage of variable region gene of mouse 6C6 monoclone antibody and constant region gene of human antibody, has been cloned and effectively expressed in CHO cells.