Phospho-RIP3 (Thr231/Ser232) (E7S1R) Rabbit mAb

Phospho-RIP3 (Thr231/Ser232) (E7S1R) Rabbit mAb Suppliers list
Company Name: Shanghai Universal Biotech Co.,Ltd  
Tel: 15921930842 15921930842
Email: yh-wang@univ-bio.com
Phospho-RIP3 (Thr231/Ser232) (E7S1R) Rabbit mAb Basic information
Source Reactivity Background References
Product Name:Phospho-RIP3 (Thr231/Ser232) (E7S1R) Rabbit mAb
Synonyms:Phospho-RIP3 (Thr231/Ser232) (E7S1R) Rabbit mAb
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Phospho-RIP3 (Thr231/Ser232) (E7S1R) Rabbit mAb Structure
Phospho-RIP3 (Thr231/Ser232) (E7S1R) Rabbit mAb Chemical Properties
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Phospho-RIP3 (Thr231/Ser232) (E7S1R) Rabbit mAb Usage And Synthesis
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BackgroundThe receptor-interacting protein family of serine-threonine kinases are important regulators of cellular stress that trigger pro-survival and inflammatory responses through the activation of NF-κB, as well as pro-apoptotic pathways. In addition to the kinase domain, RIP contains a death domain responsible for interaction with the death domain receptor Fas and recruitment to TNF-R1 through interaction with TRADD. RIP-deficient cells show a failure in TNF-mediated NF-κB activation, making the cells more sensitive to apoptosis. RIP also interacts with TNF-receptor-associated factors and can recruit IKKs to the TNF-R1 signaling complex via interaction with NEMO, leading to IκB phosphorylation and degradation. Overexpression of RIP induces both NF-κB activation and apoptosis. Caspase-8-dependent cleavage of the RIP death domain can trigger the apoptotic activity of RIP.Receptor-interacting protein 3 was originally found to interact with RIP and the TNF receptor complex to induce apoptosis and activation of NF-κB. It has subsequently been shown that the association between RIP and RIP3 is a key component of a signaling pathway that results in programmed necrosis, a necrotic-like cell death induced by TNF in the presence of caspase inhibitors. RIP3 is phosphorylated at Ser227 and targets the phosphorylation of mixed lineage kinase domain-like protein, which is critical for necroptosis. In mice, RIP3 is phosphorylated at Thr231 and Ser232, leading to association with MLKL and necroptosis.
References[1] Meylan, E. and Tschopp, J. (2005) Trends Biochem Sci 30, 151-9.
[2] Hsu, H. et al. (1996) Immunity 4, 387-96.
[3] Stanger, B.Z. et al. (1995) Cell 81, 513-23.
[4] Ting, A.T. et al. (1996) EMBO J 15, 6189-6196.
[5] Kelliher, M.A. et al. (1998) Immunity 8, 297-303.
[6] Devin, A. et al. (2000) Immunity 12, 419-429.
[7] Zhang, S.Q. et al. (2000) Immunity 12, 301-311.
[8] Lin, Y. et al. (1999) Genes Dev 13, 2514-26.
[9] Yu, P.W. et al. (1999) Curr Biol 9, 539-42.
[10] Sun, X. et al. (1999) J Biol Chem 274, 16871-5.
Phospho-RIP3 (Thr231/Ser232) (E7S1R) Rabbit mAb Preparation Products And Raw materials
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