Construction and expression of the eukaryotic expression vector containing human soluble transforming growth factor beta receptor II / 浙江大学学报·医学版
Journal of Zhejiang University. Medical sciences
;
(6): 504-508, 2004.
Article
Dans Chinois
| WPRIM
| ID: wpr-353272
ABSTRACT
<p><b>OBJECTIVE</b>To construct a eukaryotic expression vector encoding the gene of extracellular region of type II transforming growth factor beta receptor (sTGFbetaR II), to express the protein in CHO cell line and to determine its biological activity.</p><p><b>METHODS</b>The extracellular region (amino acids 1-159) of the human TGFbetaR II cDNA was amplified by PCR from a TGFbetaR II chimeric plasmid,and the eukaryotic expression plasmid pCDNA3.1/myc-his(-)B-sTGFbetaR II(pCDNA-sTGFbetaR II) was constructed by inserting the sTGFbetaR II cDNA into the EcoR I/Hind III-digested pCDNA. The DNA sequence was confirmed by double digestion and the pCDNA-sTGFbetaR II plasmid was transfected into the CHO cell line. The sTGFbetaR II protein was confirmed by Western blotting analysis and its biological function was determined.</p><p><b>RESULTS</b>The specific protein was observed in western blotting, and the protein abrogated the growth-inhibitory effects of TGF-beta1 on mink lung epithelial cells (Mv1Lu).</p><p><b>CONCLUSION</b>The eukaryotic expression plasmid pCDNA-sTGFbetaR II has been successfully constructed and the sTGFsTGFbetaR II protein with biological activity obtained.</p>
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Plasmides
/
Recombinaison génétique
/
Données de séquences moléculaires
/
Séquence nucléotidique
/
Transfection
/
Séquence d'acides aminés
/
Cellules CHO
/
Clonage moléculaire
/
Protein-Serine-Threonine Kinases
/
Récepteurs TGF-bêta
Limites du sujet:
Animaux
/
Humains
langue:
Chinois
Texte intégral:
Journal of Zhejiang University. Medical sciences
Année:
2004
Type:
Article
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