Literature DB >> 20199146

Generation and identification of monoclonal antibodies against FNIII domain D of human tenascin-C.

Yu-Cai Wang1, Lian-He Zheng, Bao-An Ma, Yong Zhou, Qing-Yu Fan.   

Abstract

Tenascin-C (TN-C), a key component of extracellular matrix (ECM), is strongly expressed in fetal and cancer tissues. Large-molecular-weight variants of TN-C, including different combinations of its alternative spliced FNIII repeats, are specifically expressed in tissues under certain pathological conditions. Here we report the production of monoclonal antibodies (MAbs) against FNIII domain D (FNIII D) of human TN-C. Complementary DNA encoding the FNIII D region was generated by RT-PCR from human osteosarcoma (OS) cell line, and the recombinant FNIII D-GST fusion protein was expressed and purified. Two hybridoma cell lines secreting monoclonal antibodies (MAbs) against FNIII D were obtained by routine murine hybridoma technique. The MAbs were identified by indirect enzyme-linked immunosorbent assay (ELISA), Western blot, and immunohistochemistry (IHC). Both of them were applicable in Western blot and IHC. With our MAbs, we found TN-C was positive in OS and most of it was among the tumor stroma. To conclude, these MAbs to human FNIII D domain of TN-C may be useful for exploring OS pathogenesis and potential clinical application.

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Year:  2010        PMID: 20199146     DOI: 10.1089/hyb.2009.0059

Source DB:  PubMed          Journal:  Hybridoma (Larchmt)        ISSN: 1554-0014


  1 in total

1.  mTOR signal transduction pathways contribute to TN-C FNIII A1 overexpression by mechanical stress in osteosarcoma cells.

Authors:  Lianhe Zheng; Dianzhong Zhang; Yunfei Zhang; Yanhua Wen; Yucai Wang
Journal:  Mol Cells       Date:  2014-02-19       Impact factor: 5.034

  1 in total

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