Department of Neurochemistry, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan.
Department of Optical Neural and Molecular Physiology, Graduate School of Biostudies, Kyoto University, Kyoto, Kyoto 606-8507, Japan.
STAR Protoc. 2022 Jun 7;3(2):101421. doi: 10.1016/j.xpro.2022.101421. eCollection 2022 Jun 17.
We present a protocol to prepare mouse cranial window implantation for two-photon wide-field calcium imaging. This protocol uses G-CaMP9a transgenic mice, which express a genetically encoded calcium indicator with high signal-to-noise ratio. We describe electroporation, followed by headplate fixation and cranial window implantation. This protocol can be used for measuring neural activity and is suitable for long-term imaging in large populations. Moreover, this protocol does not require preparation of Flp-expressing transgenic mice. For complete details on the use and execution of this protocol, please refer to Sakamoto et al. (2022).
我们提出了一种制备小鼠颅窗植入物用于双光子宽场钙成像的方案。该方案使用 G-CaMP9a 转基因小鼠,其表达具有高信噪比的基因编码钙指示剂。我们描述了电穿孔,随后是头盖骨固定板固定和颅窗植入。该方案可用于测量神经活动,适用于大群体的长期成像。此外,该方案不需要制备 Flp 表达的转基因小鼠。有关此方案的使用和执行的完整详细信息,请参阅 Sakamoto 等人(2022 年)。