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The development of antibody purification is challenging since the process aims to obtain abundant yield at a low cost while maintaining the level of product purity and quality. Purification of antibodies by ion exchange chromatography is widely used in monoclonal antibodies manufacturing. Several factors influence the binding characteristics of IgG, such as pH, conductivity or salt concentration, and linear velocity of sample loading into the column. The net surface charge of immunoglobulins, consisting of many different amino acids containing weak acidic and basic groups, will change gradually as the pH of the solution changes. In this study, we performed a simple method of anion-exchange chromatography to selectively remove impurities, using elution buffers with three different pH. Diethylaminoethyl (DEAE) sepharose fast-flow columns were used as weak anion exchanger to obtain high purity levels for IgG antibodies with a broad range of isoelectric points (pI). Increasing pH during anion-exchange chromatography increases the concentration of the dissociated form of weak acidic groups as eluant. SDS-PAGE gel electrophoresis was used to visualize the protein profiles, and monoclonal antibodies activity was determined with indirect ELISA. The result showed that anion-exchange DEAE resins were able to remove protein impurities compared to unpurified mixtures. DEAE column with Tris-Cl buffer pH 8.0 provided optimal conditions compared to pH 8.5 and 9.0. We employed a gradient salt elution procedure and achieved a high peak with 2ml fractions from 250ul of BALB/c mice ascites fluid. However, additional steps for the downstream antibody purification process are needed to meet the industrial standards. [ABSTRACT FROM AUTHOR]