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Construction of a eukaryotic expression vector of the gene encoding rat interferon-gamma-inducible protein and its expression in NIH 3T3 cells / 南方医科大学学报
Journal of Southern Medical University ; (12): 615-618, 2009.
Article Dans Chinois | WPRIM | ID: wpr-233728
ABSTRACT
<p><b>OBJECTIVE</b>To construct an expression vector of the gene encoding rat interferon-gamma-inducible protein (IP-10) and identify its expression in NIH 3T3 cells.</p><p><b>METHODS</b>IP-10 gene was amplified by polymerase chain reaction (PCR) and inserted into the eukaryotic expression vector pcDNA3.1(+). After identification by PCR, restriction endonuclease digestion and sequence analysis, the recombinant expression vector pcDNA3.1(+)-IP-10 was transfected into NIH 3T3 cells via liposome. Immunofluorescence method was used to confirm the expression of pcDNA3.1(+)-IP-10 in the transfected NIH 3T3 cells. The expression of IP-10 protein in the supernatant of the transfected cells was examined by Western blotting.</p><p><b>RESULTS</b>PCR, restriction endonuclease digestion and sequence analyses confirmed successful construction of the recombinant vector pcDNA3.1(+)-IP-10. Immunofluorescence assay identified the expression of pcDNA3.1(+)-IP-10 in NIH 3T3 cells, and the expression of IP-10 protein was detected by Western blotting in the supernatant of the transfected cells.</p><p><b>CONCLUSION</b>A eukaryotic expression vector pcDNA3.1(+)-IP-10 has been successfully constructed, which provides the basis for investigating the therapeutic effect of IP-10 on Th1 type autoimmune disease.</p>
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Plasmides / Transfection / DNA restriction enzymes / Expression des gènes / Technique d&apos;immunofluorescence / Cellules NIH 3T3 / Chimiokine CXCL10 / Vecteurs génétiques / Génétique / Métabolisme Limites du sujet: Animaux langue: Chinois Texte intégral: Journal of Southern Medical University Année: 2009 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Plasmides / Transfection / DNA restriction enzymes / Expression des gènes / Technique d&apos;immunofluorescence / Cellules NIH 3T3 / Chimiokine CXCL10 / Vecteurs génétiques / Génétique / Métabolisme Limites du sujet: Animaux langue: Chinois Texte intégral: Journal of Southern Medical University Année: 2009 Type: Article