发布: 2019年06月20日第9卷第12期 DOI: 10.21769/BioProtoc.3270 浏览次数: 4769
评审: Alessandro DidonnaDenise DrongitisAnonymous reviewer(s)
Abstract
Primary neuronal culture from rodents is a key tool in neurobiology. However, the preparation of primary cultures requires precise planning, starting from animal mating. Furthermore, each preparation generates a high amount of cells that eventually go wasted. The possibility to cryopreserve primary neural cells represents a resource for in vitro studies and significantly reduces the sacrifice of animals. Here we describe that Neurostore buffer supports the cryopreservation of primary neurons.
Keywords: Neurons (神经元)Background
Primary rodent cultures are a primary tool in any neurobiology laboratory. Primary cultures last 2-3 weeks. Therefore cells are normally prepared when necessary and employed in experiments immediately upon isolation. Cryopreservation is a routine procedure to allow long-term storage of mammalian cells. A protocol to achieve cryopreservation of neuronal cells would spare animals sacrifice and avoid the waste of cells. Furthermore, cell storage might permit the creation of cultures archive, support the reproducibility of experiments, and improve specimen sharing among different laboratories. Several studies have proposed a protocol to achieve the cryopreservation of neurons (Ichikawa et al., 2007; Paynter, 2008; Ma et al., 2010). Here we describe Neurostore, a novel buffer that promotes the long-term storage of primary mouse neurons and assures high viability upon thawing.
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文章信息
版权信息
© 2019 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Pischedda, F. and Piccoli, G. (2019). Neurostore: A Novel Cryopreserving Medium for Primary Neurons. Bio-protocol 9(12): e3270. DOI: 10.21769/BioProtoc.3270.
分类
神经科学 > 基础技术 > 低温贮藏
细胞生物学 > 细胞分离和培养 > 低温贮存
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