Title of article
Bacterial expression and purification of C1C2 domain of human factor VIII
Author/Authors
Amiri Yekta, Amir National Institute for Genetic Engineering and Biotechnology (NIGEB),Islamic Azad University of Jahrom, ايران , Zomorodipour, Alireza National Institute for Genetic Engineering and Biotechnology (NIGEB), ايران , Khodabandeh, Mahvash National Institute for Genetic Engineering and Biotechnology (NIGEB), ايران , Daliri Chopari, Morteza National Institute for Genetic Engineering and Biotechnology (NIGEB), ايران , Kafilzadeh, Farshid Islamic Azad University of Jahrom, ايران
From page
104
To page
111
Abstract
With the aim of the production of human factor VIII antigen and its corresponding antibody an epitope coding fragment of the light-chain of hFVIII, fused to a His6-tag, was isolated and over-expressed in Eschehchia coli. The over-expressed hFVIII-epitope containing peptide was confirmed by its reac- tion with a rabbit serum directed against native hFVIII as well as antiHis6-tag antibody. An expression level of 6.5 mg/l (of culture) of the C1C2-related peptide was estimated. The purified product was used to develop antibody in rabbit The immunoblotting experiment confirmed that the rabbit poly- clonal antibodies developed against the purified bacterially expressed hFVIII sub-fragment, recognizes human plasma derived FVIII. Both the produced hFVIII-related antigen and its corresponding antibody are useful in experiments using for detection and purification of hFVIII as well as the clinical diagnosis of hFVIII related disorders.
Keywords
: Human factor VIII light chain , C1C2 domain , E. coli expression system.
Journal title
Iranian Journal of Biotechnology (IJB)
Journal title
Iranian Journal of Biotechnology (IJB)
Record number
2549295
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