Cloning and eukaryotic expression of mouse Uncv gene
  
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DOI:10.3969/j.issn.1005-4847.2012.01.017
KeyWord:Uncv; clone; eukaryotic expression; hair follicle
                 
AuthorInstitution
徐嫄 北京工商大学,北京 ;军事医学科学院实验动物中心, 北京
刘冰 军事医学科学院实验动物中心, 北京
李文龙 军事医学科学院实验动物中心, 北京
胡仲明 军事医学科学院实验动物中心, 北京
曾林 军事医学科学院实验动物中心, 北京
何聪芬 北京工商大学,北京
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Abstract:
      ObjectiveTo clone the full length cDNA of Uncv gene in mice and to express the gene in eukaryotic cells.MethodsRT-PCR assay was applied to clone the full length coding region of the Uncv gene and constructed its expression plasmid pcDNA 3.1-Flag/Uncv. The recombinant plasmid was transfected into HeLa cells and the fusion protein was identified by Western blot analysis.ResultsThe complete coding sequence was obtained and cloned into the pcDNA 3.1-Flag vector. The recombinant pcDNA 3.1-Flag/Uncv plasmid was transiently expressed in HeLa cells. HeLa cell clones expressing fusion protein with molecular weight of about 95×103 were obtained. ConclusionsA recombinant eukaryotic expression plasmid of Uncv has been successfully constructed and expressed in HeLa cells. It may provide a foundation for further biological studies of Uncv gene.
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