Dataset of differential lipid raft and global proteomes of SILAC-labeled cystic fibrosis cells upon TNF -α stimulation

Cystic fibrosis (CF) is a genetic disease due to mutations in the cystic fibrosis transmembrane regulator (CFTR), F508del-CFTR being the most frequent. Lipid raft-like microdomains (LRM) are regions of the plasma membrane that present a high cholesterol content and are insoluble to non-ionic deterge...

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Bibliographic Details
Main Authors: C. Chhuon, I. Pranke, F. Borot, D. Tondelier, J. Lipecka, J. Fritsch, M. Chanson, A. Edelman, M. Ollero, I.C. Guerrera
Format: Article
Language:English
Published: Elsevier 2016-12-01
Series:Data in Brief
Online Access:http://www.sciencedirect.com/science/article/pii/S2352340916305133