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Gene-expression analysis of single cells-nested polymerase chain reaction after laser microdissection

机译:激光显微切割后单细胞嵌套聚合酶链反应的基因表达分析

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AIM: The structural and functional characteristics of cells are dependent on the specific gene expression profile. The ability to study and compare gene expression at the cellular level will therefore provide valuable insights into cell physiology and pathophysiology. METHODS: Individual cells were isolated from frozen colon tissue sections using laser microdissection. DNA as well as RNA were extracted, and total RNA was reversely transcribed to complementary DNA (cDNA). Both DNA and cDNA were analyzed by nested polymerase chain reaction (PCR). The quality of isolated DNA and RNA was satisfactory. RESULTS: Single cells were successfully microdissected using an ultraviolet laser micromanipulator. Nested PCR amplification products of DNA and cDNA of single cells could clearly be visualized by agarose gel electrophoresis. CONCLUSION: The combined use of laser microdissection and nested-PCR provides an opportunity to analyze gene expression in single cells. This method allows the analysis and identification of specific genes which are involved in physiological and pathophysiological processes in a complex of variable cell phenotypes.
机译:目的:细胞的结构和功能特征取决于特定的基因表达谱。因此,在细胞水平上研究和比较基因表达的能力将为细胞生理学和病理生理学提供有价值的见解。方法:使用激光显微切割从冷冻结肠组织切片中分离单个细胞。提取DNA和RNA,然后将总RNA反转录为互补DNA(cDNA)。通过巢式聚合酶链反应(PCR)分析DNA和cDNA。分离的DNA和RNA的质量令人满意。结果:使用紫外线激光显微操纵器成功地对单细胞进行了显微解剖。琼脂糖凝胶电泳可以清楚地观察到单个细胞DNA和cDNA的巢式PCR扩增产物。结论:激光显微切割与巢式PCR的结合使用提供了分析单细胞中基因表达的机会。该方法允许分析和鉴定在可变细胞表型复合体中涉及生理和病理生理过程的特定基因。

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