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IRAK-M Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年08月25日
  • W, IF-IC
  • Rabbit
  • H,Mk
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      IRAK-M Antibody

    • 抗原

      synthetic peptide corresponding to residues near the carboxy-terminus of human IRAK-M

    • 应用范围

      W, IF-IC

    • 宿主

      Rabbit

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 保质期

      详见说明书

    • 适应物种

      H,Mk

    • 供应商

      CST

    • 是否单克隆

      2

    • 保存条件

      -20°c

    • 规格

      40 ul (4 western blots)/100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:40 ul (4 western blots)产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting  IF-IC=Immunofluorescence (Immunocytochemistry)
    Reactivity Key:  H=Human  Mk=Monkey
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Source
    W IF-IC H Mk Endogenous 68 Rabbit
    Protocols
    Specificity / Sensitivity

    IRAK-M antibody detects endogenous levels of total IRAK-M protein. Cross reactivity was not detected with other family members.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy-terminus of human IRAK-M. Antibodies were purified by protein A and peptide affinity chromagraphy.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HL-60, Raji and K562 cell lines, using IRAK-M Antibody.

    IF-IC

    IF-IC

    Immunofluorescent analysis of THP-1 cells differentiated overnight with TPA, using IRAK-M Antibody.

    Background

    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).

    Unlike IRAK1 and IRAK4, IRAK2 and IRAK-M do not have significant kinase activity although they can still activate NF-κB when overexpressed (4). Expression of IRAK-M is more restricted compared to other family members with highest levels of expression occurring in monocytes/macrophages (4). Studies from IRAK-M knockout mice suggest that IRAK-M may play a role as a negative regulator of Toll-like receptor signaling and innate immune responses by preventing the dissociation of IRAK1 and IRAK4 from MyD88 and the subsequent formation of its complex with TRAF6 (5).

    1. Dinarello, C.A. (1996) Blood 87, 2095-147.
    2. Takaesu, G. et al. (2001) Mol Cell Biol 21, 2475-84.
    3. Janssens, S. and Beyaert, R. (2003) Mol Cell 11, 293-302.
    4. Wesche, H. et al. (1999) J. Biol. Chem. 274, 19403-10.
    5. Kobayashi, K. et al. (2002) Cell 110, 191-202.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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