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在Balb/c小鼠腹水中大规模制备和鉴定抗人CD34单克隆抗体

Large Scale Generation and Characterization of Anti-Human CD34 Monoclonal Antibody in Ascetic Fluid of Balb/c Mice.

作者信息

Aghebati Maleki Leili, Majidi Jafar, Baradaran Behzad, Abdolalizadeh Jalal, Kazemi Tohid, Aghebati Maleki Ali, Sineh Sepehr Koushan

机构信息

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. ; Tabriz International University of Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran. ; Department of Immunology, Faculty of Medicine, Tabriz University of Medical Sciences , Tabriz, Iran.

出版信息

Adv Pharm Bull. 2013;3(1):211-6. doi: 10.5681/apb.2013.035. Epub 2013 Feb 7.

Abstract

PURPOSE

Monoclonal antibodies or specific antibodies are now an essential tool of biomedical research and are of great commercial and medical value. The purpose of this study was to produce large scale of monoclonal antibody against CD34 in order to diagnostic application in leukemia and purification of human hematopoietic stem/progenitor cells.

METHODS

For large scale production of monoclonal antibody, hybridoma cells that produce monoclonal antibody against human CD34 were injected into the peritoneum of the Balb/c mice which have previously been primed with 0.5 ml Pristane. 5 ml ascitic fluid was harvested from each mouse in two times. Evaluation of mAb titration was assessed by ELISA method. The ascitic fluid was examined for class and subclasses by ELISA mouse mAb isotyping Kit. mAb was purified from ascitic fluid by affinity chromatography on Protein A-Sepharose. Purity of monoclonal antibody was monitored by SDS -PAGE and the purified monoclonal antibody was conjugated with FITC.

RESULTS

Monoclonal antibodies with high specificity and sensitivity against human CD34 by hybridoma technology were prepared. The subclass of antibody was IgG1 and its light chain was kappa.

CONCLUSION

The conjugated monoclonal antibody could be a useful tool for isolation, purification and characterization of human hematopoietic stem cells.

摘要

目的

单克隆抗体或特异性抗体如今是生物医学研究的重要工具,具有巨大的商业和医学价值。本研究的目的是大规模生产抗CD34单克隆抗体,用于白血病的诊断应用以及人造血干细胞/祖细胞的纯化。

方法

为大规模生产单克隆抗体,将产生抗人CD34单克隆抗体的杂交瘤细胞注射到预先用0.5 ml pristane预处理的Balb/c小鼠腹腔内。每只小鼠分两次采集5 ml腹水。采用ELISA法评估单克隆抗体滴度。用ELISA小鼠单克隆抗体亚型鉴定试剂盒检测腹水的类别和亚类。通过蛋白A-琼脂糖亲和层析从腹水中纯化单克隆抗体。用SDS-PAGE监测单克隆抗体的纯度,并将纯化的单克隆抗体与FITC偶联。

结果

通过杂交瘤技术制备了对人CD34具有高特异性和敏感性的单克隆抗体。抗体亚类为IgG1,轻链为kappa。

结论

偶联的单克隆抗体可能是分离、纯化和鉴定人造血干细胞的有用工具。

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