School of Biological Sciences, University of Utah, Salt Lake City, UT 84112, USA.
STAR Protoc. 2021 Mar 6;2(1):100381. doi: 10.1016/j.xpro.2021.100381. eCollection 2021 Mar 19.
Many genetically encoded tools, including large collections of GAL4 transgenic lines, can be used to visualize neurons of the brain. However, identifying transgenic lines that are expressed sparsely enough to label individual neurons, or groups of neurons that innervate a particular brain region, remains technically challenging. Here, we provide a detailed procedure in which we used broadly expressed transgenic lines and two-photon microscopy to photo-label neurons with specificity, thereby permitting their morphological characterization. For complete details on the use and execution of this protocol, please refer to Li et al. (2020).
许多基因编码工具,包括大量的 GAL4 转基因品系,可用于可视化大脑神经元。然而,鉴定表达稀疏到足以标记单个神经元或支配特定脑区的神经元群体的转基因品系仍然具有技术挑战性。在这里,我们提供了一个详细的程序,我们使用广泛表达的转基因系和双光子显微镜特异性地标记神经元,从而允许对其形态进行特征描述。有关该方案使用和执行的完整详细信息,请参考 Li 等人。(2020)。