| Literature DB >> 34159323 |
Lu Liu1, Simon Besson-Girard1, Hao Ji1, Katrin Gehring1, Buket Bulut1, Tuğberk Kaya1,2,3, Fumere Usifo1, Mikael Simons4,2,3, Ozgun Gokce1,4.
Abstract
Single-cell RNA sequencing (scRNA-seq) provides the transcriptome of individual cells and addresses previously intractable problems including the central nervous system's transcriptional responses during health and disease. However, dissociating brain cells is challenging and induces artificial transcriptional responses. Here, we describe an enzymatic dissociation method for mouse brain that prevents dissociation artifacts and lowers technical variations with standardized steps. We tested this protocol on microdissected brain tissue of 3-week- to 24-month-old mice and obtained high-quality scRNA-seq results. For complete details on the use and execution of this protocol, please refer to Safaiyan et al. (2021).Entities:
Keywords: Cell Biology; Cell isolation; Flow Cytometry/Mass Cytometry; Neuroscience; RNA-seq; Sequencing; Single Cell
Mesh:
Year: 2021 PMID: 34159323 PMCID: PMC8196224 DOI: 10.1016/j.xpro.2021.100590
Source DB: PubMed Journal: STAR Protoc ISSN: 2666-1667