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Docking Protein 7 (DOK7) (C-Term) Peptide

DOK7 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN975950
  • Target See all DOK7 products
    DOK7 (Docking Protein 7 (DOK7))
    Protein Region
    C-Term
    Origin
    Human
    Source
    • 2
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Sequence
    RAHYDTPRSL CLAPRDHSPP SQGSPGNSAA RDSGGQTSAG CPSGWLGTRR
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-DOK7 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Purification
    Purified
  • Application Notes
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    DOK7 (Docking Protein 7 (DOK7))
    Synonyms
    si:dkey-180b4.3 Peptide, si:ch211-164d19.2 Peptide, C4orf25 Peptide, CMS1B Peptide, A930013K19Rik Peptide, AW049091 Peptide, Dok-7 Peptide, EF-12 Peptide, Oit5 Peptide, RGD1566416 Peptide, dok-7 Peptide, docking protein 7 Peptide, DOK7 Peptide, dok7 Peptide, Dok7 Peptide
    Background
    The protein encoded by this gene is essential for neuromuscular synaptogenesis. The protein functions in aneural activation of muscle-specific receptor kinase, which is required for postsynaptic differentiation, and in the subsequent clustering of the acetylcholine receptor in myotubes. This protein can also induce autophosphorylation of muscle-specific receptor kinase. Mutations in this gene are a cause of familial limb-girdle myasthenia autosomal recessive, which is also known as congenital myasthenic syndrome type 1B.

    Alias Symbols: C4orf25, CMS1B, FLJ33718, FLJ39137, FLJ90556

    Protein Interaction Partner: MUSK

    Protein Size: 366
    Molecular Weight
    40 kDa
    Gene ID
    285489
    NCBI Accession
    NM_173660, NP_775931
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