首页> 外文期刊>Analusis: Chimie Analytique - Methodes Physiques d'Analyse >Differential display analysis of gene expression accompanied by neurite outgrowth of human neuroblastoma Cell IMR32 using non-gel molecular sieving capillary electrophoresis
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Differential display analysis of gene expression accompanied by neurite outgrowth of human neuroblastoma Cell IMR32 using non-gel molecular sieving capillary electrophoresis

机译:非凝胶分子筛毛细管电泳法对人神经母细胞瘤细胞IMR32基因表达伴随神经突生长的差异显示分析

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The induced proliferative response of the human derived neuroblastoma cell (IMR32), with the cell proliferation mediating factor, is much milder compared to other cell strains, and develops cellular clusters which are characterized by numerous extensions of dendrites. Presuming this phenomenon to be one of the induced neuronal differentiation due to genetic alterations, we preliminary studied to elucidate the changes in gene expression of the IMR32 by mRNA differential display analysis, monitoring polymerase chain reaction (PCR) products by non-gel molecular sieving capillary electrophoresis in linear polyacrylamide solution. The CE fingerprints revealed a number of peaks with differential expression patterns. [References: 20]
机译:与其他细胞株相比,具有细胞增殖介导因子的人源性神经母细胞瘤细胞(IMR32)诱导的增殖反应要温和得多,并且会形成以簇状树突为特征的细胞簇。假定该现象是由于遗传改变引起的神经元分化的一种现象,我们初步研究了通过mRNA差异显示分析阐明IMR32基因表达的变化,并通过非凝胶分子筛毛细管监测聚合酶链反应(PCR)产物线性聚丙烯酰胺溶液中进行电泳。 CE指纹图谱显示了许多带有差异表达模式的峰。 [参考:20]

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