Abstract

Monoclonal antibodies are key reagents that are used in biomedical researches, diagnosis of immunodeficiency diseases such as IgG subclasses deficiency and treatment of diseases like infections and cancers. For large scale production of monoclonal antibody, hybridoma cells that produce monoclonal antibody against human IgG were injected into the peritoneum of the Balb/c mice which have previously been primed with 0.5 mL Pristane. After 10 days, approximately 3 mL ascitic fluid was harvested from the peritoneum of each mouse. Ascitic fluid was assayed for the titer of monoclonal antibody in reaction with human IgG and its cross reactivity in reaction with IgM and IgA. The titer of mAb was 100,000 and didn’t show cross reactivity with IgM and IgA. Immunobloting was done for confirming the ELISA method. In immunobloting, only one sharp band in the heavy chain position of IgG was developed. The subclass of antibody was IgG1 and its light chain was kappa. Ascitic fluid was purified by ion exchange chromatography and the purified monoclonal antibody was conjugated with HRP. The conjugated monoclonal antibody could had application in diagnosis of infectious diseases like Toxoplasmosis, Rubella and IgG class of all other infectious diseases.

Highlights

  • Monoclonal antibodies are important tools used in biomedical researches, diagnosis and treatment of the diseases like infectious diseases and cancers[1,2]

  • In most diagnostic kits of the infectious diseases like Toxoplasmosis, Rubella and Cytomegalovirus, monoclonal antibodies against human IgG conjugated with enzymes, fluorochromes or radioactive labels fulfill a key role

  • The titer of monoclonal antibody in ascitic fluid was assessed by ELISA method

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Summary

Introduction

Monoclonal antibodies (mAbs) are important tools used in biomedical researches, diagnosis and treatment of the diseases like infectious diseases and cancers[1,2]. Monoclonal antibodies were produced for the first time by Milstein and Kohler[3]. These antibodies are mainly produced by clones or cell lines of Balb/c mice immunized with the requested immunogens. For large scale production of the monoclonal antibody, hybridoma cells should be reproduced by one of the flowing methods:. When hybridoma cells are injected into the peritoneum of mouse, the cells grow and produce ascitic fluid. This fluid has high concentration of antibody. The method of ascitic fluid production in peritoneum of mouse is simple and economic[5]. Antibody production in ascitic fluid can be a suitable and economical method

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