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Published on: November 7, 2010
Indirect Measurement of CRAC Channel Activity Using NFAT Nuclear Translocation by Flow Cytometry in Jurkat Cells
María D Carretta1, María A Hidalgo1, Rafael A Burgos2
1Faculty of Veterinary Science, Laboratory of Molecular Pharmacology, Institute of Pharmacology, Universidad Austral de Chile, Valdivia, Chile.
Abstract:
Flow cytometry is a powerful technology to assess the presence of NFAT in the nuclei after CRAC channel activation. Here we described a simplified procedure for the analysis of CRAC channel activity using NFAT nuclear translocation by flow cytometry, based on the isolation of Jurkat E6-1 cell nuclei.
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