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Method of Microglial DNA-RNA Purification from a Single Brain of an Adult Mouse

机译:从成年小鼠的单一脑纯化的微胶质DNA-RNA的方法

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Microglia, the resident brain immune effectors cells, show dynamic activation level changes for most neuropsychiatric diseases, reflecting their complex regulatory function and potential as a therapeutic target. Emerging single-cell molecular biology studies are used to investigate the genetic modification of individual cells to better understand complex gene regulatory pathways. Although multiple protocols for microglia isolation from adult mice are available, it is always challenging to get sufficient purified microglia from a single brain for simultaneous DNA and RNA extraction for subsequent downstream analysis. Moreover, for data comparison between treated and untreated groups, standardized cell isolation techniques are essential to decrease variability. Here, we present a combined method of microglia isolation from a single adult mouse brain, using a magnetic bead-based column separation technique, and a column-based extraction of purified DNA-RNA from the isolated microglia for downstream application. Our current method provides step-by-step instructions accompanied by visual explanations of important steps for isolating DNA-RNA simultaneously from a highly purified microglia population.
机译:微胶质细胞,静态脑免疫结果细胞,显示大多数神经精神疾病的动态激活水平变化,反映了它们复杂的调节功能和潜力作为治疗靶标。新兴单细胞分子生物学研究用于研究个体细胞的遗传修饰,以更好地理解复杂的基因调节途径。尽管可获得来自成年小鼠的微血花细胞分离的多种方案,但从单一脑中获得足够的纯化的小胶质胶质,以同时进行DNA和RNA提取以进行随后的下游分析。此外,对于处理和未处理的基团之间的数据比较,标准化的细胞隔离技术对于降低可变性至关重要。这里,我们介绍了一种使用磁珠基柱分离技术的单个成年小鼠脑的微胶质细胞分离的组合方法,以及来自分离的微胶质的基于纯化的DNA-RNA的柱子的下游施用。我们的目前的方法提供了逐步说明的指令,其目的是从高度纯化的微胶质群中同时分离DNA-RNA的重要步骤。

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