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本文引用的文献

1
Immune Defense Protein Expression in Highly Purified Mouse Lung Epithelial Cells.高纯度小鼠肺上皮细胞中的免疫防御蛋白表达
Am J Respir Cell Mol Biol. 2016 Jun;54(6):802-13. doi: 10.1165/rcmb.2015-0171OC.

通过流式细胞术细胞分选分离高纯度原代小鼠II型肺泡上皮细胞

Isolation of Highly Pure Primary Mouse Alveolar Epithelial Type II Cells by Flow Cytometric Cell Sorting.

作者信息

Sinha Meenal, Lowell Clifford A

机构信息

Department of Laboratory Medicine and the Program in Immunology, University of California, San Francisco, USA.

出版信息

Bio Protoc. 2016 Nov 20;6(22). doi: 10.21769/BioProtoc.2013.

DOI:10.21769/BioProtoc.2013
PMID:28180137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5293249/
Abstract

In this protocol, we describe the method for isolating highly pure primary alveolar epithelial type II (ATII) cells from lungs of naïve mice. The method combines negative selection for a variety of lineage markers along with positive selection for EpCAM, a pan-epithelial cell marker. This method yields 2-3 × 10 ATII cells per mouse lung. The cell preps are highly pure and viable and can be used for genomic or proteomic analyses or cultured to understand their roles in various biological processes.

摘要

在本方案中,我们描述了从未经处理的小鼠肺中分离高纯度原代II型肺泡上皮细胞(ATII)的方法。该方法结合了对多种谱系标志物的阴性选择以及对全上皮细胞标志物EpCAM的阳性选择。此方法每只小鼠肺可产生2 - 3×10个ATII细胞。细胞制备物高度纯净且具有活力,可用于基因组或蛋白质组分析,或进行培养以了解它们在各种生物学过程中的作用。