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1.
Journal of Southern Medical University ; (12): 433-436, 2009.
Artículo en Chino | WPRIM | ID: wpr-233770

RESUMEN

<p><b>OBJECTIVE</b>To construct an eukaryotic coexpression vector containing Mycobacterium tuberculosis heat shock protein 70 (mtHSP70) and enhanced green fluorescent protein (EGFP) controlled by cytomegalovirus promoter using pIRES-EGFP vector.</p><p><b>METHODS</b>The mtHSP70 gene fragment was amplified by PCR from pVAX-mtHSP70-HSV2gD using specific primers. The PCR product was cloned into the vector pMD 18-T vector, and the correct clone was selected according to DNA sequence analysis. The interested mtHSP70 gene fragment was subcloned into pCMV-IRES-EGFP vector with XhoI and EcoR I digestion. The recombinant plasmid was transfected into mouse melanoma B16 cell line, and the green fluorescent cells were detected by fluorescence microscopy and mtHSP70 expression was detected by Western blotting.</p><p><b>RESULTS</b>The recombinant plasmid obtained was confirmed by enzyme digestion. The transfected mouse melanoma B16 cells exhibited green fluorescence under fluorescence microscopy and expressed mtHSP70 protein as demonstrated by Western blotting.</p><p><b>CONCLUSION</b>The eukaryotic coexpression vector PCMV-mtHSP70-IRES-EGFP has been established to allow further investigation of the role of mtHSP70 gene in tumor immunotherapy.</p>


Asunto(s)
Animales , Ratones , Secuencia de Bases , Vacunas contra el Cáncer , Línea Celular Tumoral , Citomegalovirus , Genética , Metabolismo , Vectores Genéticos , Genética , Proteínas Fluorescentes Verdes , Genética , Proteínas HSP70 de Choque Térmico , Genética , Datos de Secuencia Molecular , Mycobacterium tuberculosis , Metabolismo , Proteínas Recombinantes de Fusión , Genética , Análisis de Secuencia de ADN
2.
Chinese Journal of Stomatology ; (12): 74-77, 2007.
Artículo en Chino | WPRIM | ID: wpr-292961

RESUMEN

<p><b>OBJECTIVE</b>To investigate the effect of inducible nitric oxide synthase (iNOS) on vascular endothelial growth factor (VEGF) expression.</p><p><b>METHODS</b>The vector containing short hairpin RNA of iNOS was transfected into Tca8113 cells using the RNA interference (RNAi) technique. The gene and protein expression of iNOS and VEGF was examined by RT-PCR and Western blot.</p><p><b>RESULTS</b>The expression of iNOS, VEGF gene in Tca8113 cells was significantly different between the experimental and control groups 24 h and 48 h after transfection (P < 0.05). The protein expression of iNOS was different between the two groups 36 h and 48 h after transfection, and of VEGF was also different between the two groups 48 h after transfection (P < 0.05).</p><p><b>CONCLUSIONS</b>The expression of VEGF could be down-regulated by silencing the iNOS gene in Tca8113 cells.</p>


Asunto(s)
Humanos , Carcinoma de Células Escamosas , Genética , Metabolismo , Línea Celular Tumoral , Regulación hacia Abajo , Regulación Neoplásica de la Expresión Génica , Óxido Nítrico Sintasa de Tipo II , Genética , Interferencia de ARN , Neoplasias de la Lengua , Genética , Metabolismo , Factor A de Crecimiento Endotelial Vascular , Genética , Metabolismo
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