DAPK1 Antibody

DAPK1 Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月18日
  • W
  • Rabbit
  • H,M,R,Mk
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    • 技术资料
    • 抗体英文名

      DAPK1 Antibody

    • 抗原

      synthetic peptide corresponding to residues surrounding Gly903 of human DAPK1

    • 应用范围

      W

    • 宿主

      Rabbit

    • 库存

      大量

    • 供应商

      CST

    • 适应物种

      H,M,R,Mk

    • 级别

      详见MSDS文件

    • 保质期

      详见说明书

    • 是否单克隆

      2

    • 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
    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) Source
    W H M R (Mk) Endogenous 160 Rabbit
    Protocols
    Specificity / Sensitivity

    DAPK1 Antibody detects endogenous levels of total DAPK1 protein.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Gly903 of human DAPK1. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell lines using DAPK1 Antibody.

    Background

    Death-associated protein kinase (DAPK1) is a Ca2+ /calmodulin-regulated serine/threonine kinase that participates in a wide range of apoptotic signals including interferon-γ, tumor necrosis factor α, Fas, activated c-Myc, and detachment from the extracellular matrix. In addition to the kinase domain and calmodulin regulatory segment, DAPK1 also has eight ankyrin repeats, a cytoskeleton binding region, and a conserved death domain (1-3). Deletion of the calmodulin-regulatory domain generates a constitutively active mutant kinase. Ectopic expression of wild-type DAPK1 induced cell death in HeLa cells. Conversely, expression of a catalytically inactive mutant protected cells from interferon-γ-induced cell death (4). The catalytic domain of DAPK1 has very high sequence similarity to vertebrate myosin light chain kinase (MLCK) and a RXX(S/T)X motif derived from myosin light chain protein was shown to be phosphorylated in vitro by DAPK1 (5).

    Epigenetic silencing of DAPK1 by promoter methylation has been observed in cases of chronic lymphocytic leukemia (6,7).

    1. Kimchi, A. (1999) Ann Rheum Dis. 58, I14-I19.
    2. Cohen, O. et al. (1999) J Cell Biol 146, 141-148.
    3. Deiss, L. P. et al. (1995) Genes Dev 9, 15-30.
    4. Cohen, O. et al. (1997) EMBO J 16, 998-1008.
    5. Velentza, A. V. et al. (2001) J Biol Chem 276, 38956-38965.
    6. Raval, A. et al. (2007) Cell 129, 879-890.
    7. Katzenellenbogen, R.A. et al. (1999) Blood 93, 4347-4353.
    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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