发布: 2013年11月20日第3卷第22期 DOI: 10.21769/BioProtoc.973 浏览次数: 17283
评审: Xuecai Ge
相关实验方案
使用康可藻红素刺激冷冻保存的猪外周单个核细胞进行增殖检测,并结合FCS ExpressTM 7.18软件分析
Marlene Bravo-Parra [...] Luis G. Giménez-Lirola
2025年06月05日 1640 阅读
Abstract
Flow cytometry, a standard technique used for quantitative analysis of isolated cells, is routinely employed by immunologists and oncologists to study DNA content, protein expression, and other functional parameters in blood and tumor cells. Unfortunately, the use of this technique by neurobiologists has been hampered by the complexity of the nervous system, whose constituting cells can hardly be dissociated to obtain samples of sufficient quality. We have developed a simplified and quick method to purify and immunolabel cell nuclei with high sensitivity and low background. Our protocol allows the discrimination of single nuclei from doublets and larger aggregates, obtaining low coefficients of variation for cell cycle analysis with propidium iodide. In addition, due to the reduced sample handling this method has high recovery and good reproducibility. As an example, in this protocol we describe the isolation of cell nuclei from adult cerebral cortex, which are subsequently immunostained with antibodies against NeuN (a general neuronal marker) and EGR1 (an early response gene expressed by functionally active neurons), and subjected to flow cytometric gating and analysis. Nevertheless, the protocol can also be applied to other neural tissues from adult and embryonic brain.
Keywords: Flow cytometry (流式细胞仪)Materials and Reagents
Equipment
Software
Procedure
文章信息
版权信息
© 2013 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Readers should cite both the Bio-protocol article and the original research article where this protocol was used:
分类
神经科学 > 细胞机理
细胞生物学 > 基于细胞的分析方法 > 流式细胞术
细胞生物学 > 细胞器分离 > 细胞核
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