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HES7 antibody

HES7 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5027718
  • Target See all HES7 Antibodies
    HES7 (Hairy and Enhancer of Split 7 (HES7))
    Reactivity
    • 47
    • 21
    • 11
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    Human
    Host
    • 47
    • 1
    Rabbit
    Clonality
    • 48
    Polyclonal
    Conjugate
    • 14
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This HES7 antibody is un-conjugated
    Application
    • 21
    • 20
    • 13
    • 13
    • 4
    • 4
    • 3
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Protein A Chromatography
    Immunogen
    Full length recombinant Hes7 protein was used as the immunogen for this antibody.
    Isotype
    IgG
    Top Product
    Discover our top product HES7 Primary Antibody
  • Application Notes
    WB: 0.5-1 μg/mL
    Restrictions
    For Research Use only
  • Concentration
    0.5 mg/mL
    Buffer
    PBS containing 0.05 % BSA, PH 7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store the antibody at 4°C, stable for 6 months. For long-term storage, store at -20°C. Avoid repeated freeze and thaw cycles.
  • Target
    HES7 (Hairy and Enhancer of Split 7 (HES7))
    Alternative Name
    Hes7 (HES7 Products)
    Synonyms
    SCDO4 antibody, bHLHb37 antibody, hes family bHLH transcription factor 7 antibody, hairy and enhancer of split 7 (Drosophila) antibody, HES7 antibody, Hes7 antibody
    Background
    HES7 (Hes family bHLH transcription factor 7) is a member of the Hairy-and-enhancer-of-split (HES) family of transcription factors, which play a role in somite formation. This is expressed in an oscillatory manner during the process of somitogenesis, a process by which somites (bilaterally paired blocks of mesoderm) form and give rise to skeletal muscle, cartilage, tendons, endothelial cells, and dermis. Missense mutations of HES7 have been reported to cause SCDO4 (Spondylocostal Dysostosis 4), an inherited disorder that is characterized by the presence of extensive hemivertebrae, truncal shortening and abnormally aligned ribs.
    Molecular Weight
    25 kDa
    Gene ID
    84667
    UniProt
    Q9BYE0
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