Your browser doesn't support javascript.
loading
Purification of anti-HBcAg monoclonal antibodies using immobilized metal ion affinity chromatography / 生物工程学报
Chinese Journal of Biotechnology ; (12): 1572-1578, 2009.
Article in Chinese | WPRIM | ID: wpr-296888
ABSTRACT
Anti-HBcAg monoclonal antibodies from mouse ascites were purified by using immobilized metal ion affinity chromatography. We optimized the conditions of sample loading and elution. The results showed that when the pH stepwise elution was used, the best solution for sample loading was 20 mmol/L phosphate buffer containing 0.5 mol/L sodium chloride at pH 8.0 and the mAb was eluted at pH 5.0. The purity of obtained mAb was more than 85% and recovery reached 80%. When the adsorbed proteins were eluted by using gradient elution of an imidazole, the best solution for loading condition was 20 mmolL phosphate buffer containing 5 mmol/L imidazole at pH 8.0. The purity and recovery of antibody were up to 95%.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Chemistry / Chromatography, Affinity / Chromatography, Ion Exchange / Allergy and Immunology / Hepatitis B Core Antigens / Hydrogen-Ion Concentration / Imidazoles / Metals / Methods / Antibodies, Monoclonal Limits: Animals Language: Chinese Journal: Chinese Journal of Biotechnology Year: 2009 Type: Article

Similar

MEDLINE

...
LILACS

LIS

Full text: Available Index: WPRIM (Western Pacific) Main subject: Chemistry / Chromatography, Affinity / Chromatography, Ion Exchange / Allergy and Immunology / Hepatitis B Core Antigens / Hydrogen-Ion Concentration / Imidazoles / Metals / Methods / Antibodies, Monoclonal Limits: Animals Language: Chinese Journal: Chinese Journal of Biotechnology Year: 2009 Type: Article