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Neuroscience Neurotransmission Intracellular Signaling Kinases

Anti-DRAK2 antibody (ab8419)

Anti-DRAK2 antibody (ab8419)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Rabbit polyclonal to DRAK2
  • Suitable for: WB, ICC/IF
  • Reacts with: Human
  • Isotype: IgG

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Overview

  • Product name

    Anti-DRAK2 antibody
    See all DRAK2 primary antibodies
  • Description

    Rabbit polyclonal to DRAK2
  • Host species

    Rabbit
  • Tested Applications & Species

    Application Species
    ICC/IF
    Human
    WB
    Human
    See all applications and species data
  • Immunogen

    Synthetic peptide:

    CSKRFRFDDSLPNPHE

    , corresponding to amino acids 351/365 of Human DRAK2. (Peptide available as ab8454.)
    Run BLAST with BLAST the sequence with ExPASy Run BLAST with BLAST the sequence with NCBI
  • Positive control

    • Wholecell lysate from Jurkat cells An approximately 45 kDa band can be detected.
  • General notes


    Apoptosis is mediated by death domain containing adapter molecules and a caspase family of proteases. Certain serine/threonine protein kinases, such as ASK-1 and RIP,are mediators of apoptosis. Two novel serine/threonine kinases that induce apoptosis were recently identified and designated DRAK1 and DRAK2 (for DAP kinase-related apoptosis-inducing protein kinases) (1). DRAKs contain anN-terminal kinase domain and a C-terminal regulation domain. Overexpression of DRAK2 induces apoptosis. DRAKs have high sequence homology to DAP and ZIP kinases, and they represent a novel family of serine/threonine kinases, which mediates apoptosis through their catalytic activities. DRAK2 is located in nucleus and the messenger RNA was ubiquitously expressed in human tissues.

Properties

  • Form

    Liquid
  • Storage instructions

    Shipped at 4°C. Store at +4°C.
  • Storage buffer

    pH: 7.2
    Preservative: 0.02% Sodium azide
  • Concentration information loading...
  • Purity

    Ion Exchange Chromatography
  • Purification notes

    DRAK2 Antibody is Ion exchange chromatography purified.
  • Primary antibody notes

    Apoptosis is mediated by death domain containing adapter molecules and a caspase family of proteases. Certain serine/threonine protein kinases, such as ASK-1 and RIP,are mediators of apoptosis. Two novel serine/threonine kinases that induce apoptosis were recently identified and designated DRAK1 and DRAK2 (for DAP kinase-related apoptosis-inducing protein kinases) (1). DRAKs contain anN-terminal kinase domain and a C-terminal regulation domain. Overexpression of DRAK2 induces apoptosis. DRAKs have high sequence homology to DAP and ZIP kinases, and they represent a novel family of serine/threonine kinases, which mediates apoptosis through their catalytic activities. DRAK2 is located in nucleus and the messenger RNA was ubiquitously expressed in human tissues.
  • Clonality

    Polyclonal
  • Isotype

    IgG
  • Light chain type

    unknown
  • Research areas

    • Cell Biology
    • Apoptosis
    • Intracellular
    • Kinases
    • Signal Transduction
    • Protein Phosphorylation
    • Ser / Thr Kinases
    • Other Kinases

Images

  • Western blot - Anti-DRAK2 antibody (ab8419)
    Western blot - Anti-DRAK2 antibody (ab8419)
    Lane 1 : Anti-DRAK2 antibody (ab8419) at 1 µg/ml (DRAK2 antibody)
    Lane 2 : Anti-DRAK2 antibody (ab8419) at 2 µg/ml (DRAK2 antibody)

    All lanes : Raji cell lysate

    Predicted band size: 43 kDa

  • Western blot - Anti-DRAK2 antibody (ab8419)
    Western blot - Anti-DRAK2 antibody (ab8419)
    All lanes : Anti-DRAK2 antibody (ab8419) at 1/500 dilution

    Lane 1 : Jurkat whole cell lysate with absence of blocking peptide
    Lane 2 : Raji whole cell lysate with absence of blocking peptide
    Lane 3 : Jurkat whole cell lysate with presence of blocking peptide
    Lane 4 : Raji whole cell lysate with presence of blocking peptide

    Predicted band size: 43 kDa
    Observed band size: 45 kDa
    why is the actual band size different from the predicted?



    We are unsure about the nature of the 70 kDa band. However, DRAK2 is autophosphorylated and it is possible that this band corresponds to the phosphorylated form. The fact that the detection of this band is blocked by DRAK2 peptide indicates that it probably is closely related to the DRAK2 protein.
  • Immunocytochemistry/ Immunofluorescence - Anti-DRAK2 antibody (ab8419)
    Immunocytochemistry/ Immunofluorescence - Anti-DRAK2 antibody (ab8419)

    ab8419 at 10µg/ml staining DRAK2 in Jurkat cells by ICC/IF

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

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