| Literature DB >> 33364620 |
Shinichiro Okamoto1,2,3, Kenta Yamauchi1,2, Jaerin Sohn4, Megumu Takahashi1,3, Yoko Ishida1, Takahiro Furuta5, Masato Koike1,2, Fumino Fujiyama6, Hiroyuki Hioki1.
Abstract
We developed an adeno-associated virus (AAV) vector-based technique to label mouse neostriatal neurons comprising direct and indirect pathways with different fluorescent proteins and analyze their axonal projections. The AAV vector expresses GFP or RFP in the presence or absence of Cre recombinase and should be useful for labeling two cell populations exclusively dependent on its expression. Here, we describe the AAV vector design, stereotaxic injection of the AAV vector, and a highly sensitive immunoperoxidase method for axon visualization. For complete details on the use and execution of this protocol, please refer to Okamoto et al. (2020).Entities:
Keywords: Gene Expression; Microscopy; Neuroscience
Mesh:
Substances:
Year: 2020 PMID: 33364620 PMCID: PMC7753197 DOI: 10.1016/j.xpro.2020.100230
Source DB: PubMed Journal: STAR Protoc ISSN: 2666-1667