发布: 2013年05月05日第3卷第9期 DOI: 10.21769/BioProtoc.754 浏览次数: 49432
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Kristina Seiler [...] Mario P. Tschan
2023年07月20日 1560 阅读
Abstract
Subcellular localization is crucial for the proper functioning of a protein. Deregulation of subcellular localization may lead to pathological consequences and result in diseases like cancer. Immuno-fluorescent staining and subcellular fractionation can be used to determine localization of a protein. Here we discuss a protocol to separate the nuclear, cytosolic, and membrane fractions of cultured human cell lines using a centrifuge and ultracentrifuge. The membrane fraction contains plasma membranes and ER-golgi membranes, but no mitochondria or nuclear structures. The fractions can be further analyzed using Western blotting. This protocol is based on that from Dr. Richard Patten at Abcam, and was modified and utilized in a publication by Huang et al. (2012).
Keywords: Nuclear (细胞核)Materials and Reagents
Equipment
Procedure
文章信息
版权信息
© 2013 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Yu, Z., Huang, Z. and Lung, M. L. (2013). Subcellular Fractionation of Cultured Human Cell Lines. Bio-protocol 3(9): e754. DOI: 10.21769/BioProtoc.754.
分类
癌症生物学 > 通用技术 > 生物化学试验
生物化学 > 蛋白质 > 分离和纯化
细胞生物学 > 细胞器分离 > 分级分离
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