Somayeh Sadeghi - Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
Leili Aghebati-Maleki - Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
Samira Nozari - Department of Immunology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
Jafar Majidi - Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran

Antibodies are a class of biomolecules that has an important role in the immune system and lots of applications in biotechnological methods and in pharmaceutics. Production and purification of antibodies in laboratory animals is one of the first ways to manufacture of these prominent tools. The obtained antibodies from these process could be used in various types of bioassay techniques such as enzyme linked immunosorbent assay (ELISA), radioimmunoassay, etc. Also, antibodies employed in diagnostics applications in humans and other animals in order to detect specific antigens.In this study, we aimed to produce and purify anti-dog IgG via immunizing rabbits with dog IgG in combination with Freund's adjuvant. Polyclonal IgG were purified by ion exchange chromatography and then the purified antibody was labeled with horse radish peroxidase (HPR). Direct ELISA was used to determine the optimum titer and cross-reactivity of HRP conjugated IgG. The purity of various IgG preparations and the optimum dilution of prepared HRP conjugated IgG, respectively, was about ۹۵.۰۰% and ۱:۸۰۰۰. This study showed that efficiency ion-exchange chromatography could be an appropriate method for purification of IgG antibodies. This antibody could be a useful tool for future dog immune diagnosis tests. This product characterization shown here sets the foundations for future work on dog IgGs.

Anti-dog IgG, ‎ HRP-conjugation, ‎ Ion-exchange chromatography, ‎ Polyclonal antibody