发布: 2015年10月05日第5卷第19期 DOI: 10.21769/BioProtoc.1608 浏览次数: 10307
评审: Oneil G. BhalalaPamela MaherGeoff Lau
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蚊虫和白蛉中肠组织的优化解离方法:用于高质量单细胞RNA测序
Ana Beatriz F. Barletta [...] Carolina Barillas-Mury
2025年06月20日 1286 阅读
Abstract
The neural tube explant culture technique allows in vitro culturing of small pieces of neural tissue isolated from e.g., chick or mouse embryonic tissue in a matrix of collagen for defined periods of time. This method can be used to study the effects of defined molecules on developmental processes such as neural progenitor proliferation and neuronal differentiation and/or survival. Since the explant material can also be prepared from embryonic tissue electroporated with expression vectors, this technique can be adapted to study gene function in the presence of specific environmental signals. Different regions of the neural tube can also be isolated during the dissection step, allowing specific regions of the neural tube to be studied separately. Here, we present a neural tube explant culture method that we have used in several studies (Dias et al., 2014; Lek et al., 2010; Vallstedt et al., 2005).
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版权信息
© 2015 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Alekseenko, Z., Andersson, E. and Dias, J. M. (2015). Chick Neural Tube Explant Culture. Bio-protocol 5(19): e1608. DOI: 10.21769/BioProtoc.1608.
分类
神经科学 > 发育 > 外植体培养
细胞生物学 > 组织分析 > 组织分离
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