Site-Specific Detection of Tyrosine Phosphorylated CD95 Following Protein Separation by Conventional and Phospho-Protein Affinity SDS-PAGE

Autor: Sébastien Huault, Krittalak Chakrabandhu, Anne-Odile Hueber
Přispěvatelé: Institut de Biologie Valrose (IBV), Université Nice Sophia Antipolis (... - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA)
Rok vydání: 2017
Předmět:
Zdroj: Methods in Molecular Biology ISBN: 9781493967780
CD95
CD95, 1557, Springer New York, pp.173-188, 2017, Methods in Molecular Biology, ⟨10.1007/978-1-4939-6780-3_16⟩
Methods Mol Biol
Methods Mol Biol, 1557, pp.173-188, 2017, ⟨10.1007/978-1-4939-6780-3_16⟩
Popis: International audience; Phosphorylation of two tyrosines in the death domain of CD95 is a critical mechanism in determining the receptor's choices between cell death and survival signals. Recently, site-specific monoclonal antibodies against phosphorylated tyrosines of CD95 have been generated and used to successfully detect each phosphorylated death domain tyrosine of CD95 directly and separately by immunoblotting. Here we provide detailed protocols and useful tips for a successful site-specific detection of phosphorylated death domain tyrosine of CD95 following a protein separation by sizes (conventional SDS-PAGE) and by degrees of phosphorylation (phospho-protein affinity, mobility shift SDS-PAGE).
Databáze: OpenAIRE