IRF-3 (D83B9) Rabbit mAb产品图

IRF-3 (D83B9) Rabbit mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2026年05月29日
  • W, IP
  • H,M,R,Mk
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      IRF-3 (D83B9) Rabbit mAb

    • 抗原

      synthetic peptide corresponding to residues near the carboxyl terminus of human IRF-3

    • 应用范围

      W, IP

    • 级别

      详见MSDS文件

    • 保质期

      详见说明书

    • 供应商

      CST

    • 适应物种

      H,M,R,Mk

    • 库存

      大量

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

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

    规格: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  IP=Immunoprecipitation
    Reactivity Key:  H=Human  M=Mouse  R=Rat  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) Isotype
    W IP H M R Mk Endogenous 45-55 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    IRF-3 (D83B9) Rabbit mAb detects endogenous levels of total IRF-3 protein.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxyl terminus of human IRF-3.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from COS-7 cells, mock transfected or transfected with human, mouse or rat IRF-3 constructs, using IRF-3 (D83B9) Rabbit mAb. The human and mouse constructs contain epitope tags.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell lines using IRF-3 (D83B9) Rabbit mAb.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from differentiated THP-1 cells, untreated or treated with LPS (1 µ g/ml, 1 hour), using Phospho-IRF-3 (Ser396) (4D4G) Rabbit mAb #4947 (upper) or IRF-3 (D83B9) Rabbit mAb (lower).


    Background

    Interferon regulatory factors (IRFs) comprise a family of transcription factors that function within the Jak/Stat pathway to regulate interferon (IFN) and IFN-inducible gene expression in response to viral infection (1). IRFs play an important role in pathogen defense, autoimmunity, lymphocyte development, cell growth, and susceptibility to transformation. The IRF family includes nine members: IRF-1, IRF-2, ISGF3γ/p48, IRF-3, IRF-4 (Pip/LSIRF/ICSAT), IRF-5, IRF-6, IRF-7, and IRF-8/ICSBP. All IRF proteins share homology in their amino-terminal DNA-binding domains. IRF family members regulate transcription through interactions with proteins that share similar DNA-binding motifs, such as IFN-stimulated response elements (ISRE), IFN consensus sequences (ICS), and IFN regulatory elements (IRF-E) (2).

    IRF-3 can inhibit cell growth and plays a critical role in controlling the expression of genes in the innate immune response (1-4). In unstimulated cells, IRF-3 is present in the cytoplasm. Viral infection results in phosphorylation of IRF-3 and leads to its translocation to the nucleus where it activates promoters containing IRF-3-binding sites. Phosphorylation of IRF-3 occurs at a cluster of carboxyl-terminal serine and threonine residues (between 385 and 405) leading to its association with the p300/CBP coactivator protein that promotes DNA binding and transcriptional activity (5). During infection, IRF-3 is likely activated through a pathway that includes activation of Toll-like receptors and of a kinase complex that includes IKKε and TBK1 (6,7). IRF-3 is phosphorylated at Ser396 following viral infection, expression of viral nucleocapsid, and double stranded RNA treatment. These events likely play a role in activation of IRF-3 (8).

    1. Taniguchi, T. et al. (2001) Annu Rev Immunol 19, 623-55.
    2. Honda, K. and Taniguchi, T. (2006) Nat Rev Immunol 6, 644-58.
    3. Hiscott, J. et al. (1999) J Interferon Cytokine Res 19, 1-13.
    4. Kim, T.Y. et al. (2003) J Biol Chem 278, 15272-8.
    5. Yoneyama, M. et al. (2002) J Interferon Cytokine Res 22, 73-6.
    6. Fitzgerald, K.A. et al. (2003) Nat Immunol 4, 491-6.
    7. Kopp, E. and Medzhitov, R. (2003) Curr Opin Immunol 15, 396-401.
    8. Servant, M.J. et al. (2003) J Biol Chem 278, 9441-7.
    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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    图标文献和实验
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    [10]Peroxiredoxin 1 Interacts with TBK1/IKKε and Negatively Regulates Pseudorabies Virus Propagation by Promoting Innate Immunity.
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