Product Pathways - NF-kB Signaling
Phospho-IRAK4 (Thr345/Ser346) Antibody #7652
|7652S||100 µl (10 western blots)||---||In Stock||---|
|7652||carrier free and custom formulation / quantity||email request|
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Species cross-reactivity is determined by western blot.
Applications Key: W=Western Blotting
Species predicted to react based on 100% sequence homology: Mouse, Rat, Monkey, Bovine, Dog.
Specificity / Sensitivity
Phospho-IRAK4 (Thr345/Ser346) Antibody recognizes endogenous levels of IRAK4 protein only when phosphorylated at Thr345 and Ser346. The antibody may also react with single phosphorylation of IRAK4 at Ser346.
Source / Purification
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Thr345/Ser346 of human IRAK4 protein. Antibodies are purified by protein A and peptide affinity chromatography.
Western blot analysis of serum-starved KARPAS-299 cells, untreated or treated with Human Interleukin-1β (hIL-1β) #8900 (50 ng/ml, 15 min), using Phospho-IRAK4 (Thr345/Ser346) Antibody (upper) or total IRAK4 Antibody #4363 (lower). Cell Line Source: Dr Abraham Karpas at the University of Cambridge.
Interleukin-1 (IL-1) receptor-associated kinase (IRAK) is a serine/threonine-specific kinase that can be coprecipitated in an IL-1-inducible manner with the IL-1 receptor (1). The mammalian family of IRAK molecules contains four members (IRAK1, IRAK2, IRAK3/IRAK-M, and IRAK4). The binding of IL-1 to IL-1 receptor type I (IL-1RI) initiates the formation of a complex that includes IL-1RI, AcP, MyD88, and IRAKs (2). IRAK undergoes autophosphorylation shortly after IL-1 stimulation. The subsequent events involve IRAK dissociation from the IL-1RI complex, its ubiquitination, and its association with two membrane-bound proteins: TAB2 and TRAF6. The resulting IRAK-TRAF6-TAB2 complex is then released into the cytoplasm where it activates protein kinase cascades, including TAK1, IKKs, and the stress-activated kinases (3).
Upon IL-1R/Toll-Like Receptor ligation, IRAK1 and IRAK4 are rapidly recruited to the receptor by the adaptor MyD88 (4). IRAK1 is phosphorylated by IRAK4 at Thr209 and Thr387 (5), followed by sequential autohyperphosphorylation in various domains.
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