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使用 EdU 掺入和多色流式细胞术分析小鼠神经干细胞和祖细胞的增殖。

Analyzing mouse neural stem cell and progenitor cell proliferation using EdU incorporation and multicolor flow cytometry.

机构信息

Department of Pharmacology, Physiology and Neurosciences, Rutgers-NJMS, Newark, NJ 07103, USA.

ICON Laboratory Services, Farmingdale, NY 11735, USA.

出版信息

STAR Protoc. 2021 Dec 23;3(1):101065. doi: 10.1016/j.xpro.2021.101065. eCollection 2022 Mar 18.

Abstract

This protocol describes an approach to identify and quantify the proportions of proliferating neural stem cells and progenitors of the mouse subventricular zone. It uses ethynyl deoxyuridine (EdU) incorporation to identify dividing cells, combined with multicolor flow cytometry for 4 cell surface antigens to distinguish between 8 phenotypically distinct mouse neural progenitors and stem cells. It has been optimized for wild-type neonatal mice but can be used on mice of any postnatal age. For complete details on the use and execution of this profile, please refer to Kumari et al. (2020).

摘要

本方案描述了一种鉴定和定量分析小鼠侧脑室下区增殖神经干细胞和祖细胞比例的方法。它使用 5-乙炔基-2-脱氧尿苷(EdU)掺入来识别分裂细胞,结合多色流式细胞术检测 4 种细胞表面抗原,以区分 8 种表型不同的小鼠神经祖细胞和干细胞。该方案已针对新生野生型小鼠进行了优化,但也可用于任何出生后年龄的小鼠。有关该方案使用和执行的详细信息,请参考 Kumari 等人(2020 年)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0027/8718722/a8d63e2b2b9f/fx1.jpg

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