Protocol for the isolation and culture of mouse dorsal root ganglion neurons for imaging applications.

Protocol for the isolation and culture of mouse dorsal root ganglion neurons for imaging applications.
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DOI:
10.1016/j.xpro.2023.102717
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发表时间:
2023-12-15
期刊:
影响因子:
--
通讯作者:
Campbell, Zachary T.
Campbell, Zachary T.
中科院分区:
其他
文献类型:
--
作者:
Smith, Patrick R.;Meyer, Angela;Loerch, Sarah;Campbell, Zachary T.

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Sensory neurons play pervasive roles throughout biology. In vitro studies to probe their functions hinge on the successful application of primary cell culture. Here, we present a protocol for the isolation and culture of mouse dorsal root ganglion neurons for imaging applications. We describe steps for extracting dorsal root ganglia, preparing cultures, maintaining them for days in vitro, and performing immunocytochemical labeling. We also include special considerations with respect to additional downstream applications. For complete details on the use and execution of this protocol, please refer to Smith et al. (2021). Detailed protocol for how to culture primary sensory neurons from mice Primary cultures are amenable for imaging applications Incubation for up to six days allows for neurite outgrowth Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics. Sensory neurons play pervasive roles throughout biology. In vitro studies to probe their functions hinge on the successful application of primary cell culture. Here, we present a protocol for the isolation and culture of mouse dorsal root ganglion neurons for imaging applications. We describe steps for extracting dorsal root ganglia, preparing cultures, maintaining them for days in vitro, and performing immunocytochemical labeling. We also include special considerations with respect to additional downstream applications.
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