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HES7 antibody

HES7 Reactivity: Human, Mouse ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7245221
  • Target See all HES7 Antibodies
    HES7 (Hairy and Enhancer of Split 7 (HES7))
    Reactivity
    • 47
    • 20
    • 11
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    Human, Mouse
    Host
    • 47
    • 1
    Rabbit
    Clonality
    • 48
    Polyclonal
    Conjugate
    • 14
    • 5
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This HES7 antibody is un-conjugated
    Application
    • 21
    • 21
    • 13
    • 13
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of human HES7
    Isotype
    IgG
    Top Product
    Discover our top product HES7 Primary Antibody
  • Application Notes
    IHC 1:30-1:150, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.72 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, 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
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / 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
    This gene encodes a member of the hairy and enhancer of split family of bHLH transcription factors. The mouse ortholog of this gene is regulated by Notch signaling. The protein functions as a transcriptional repressor, and is implicated in correct patterning of the axial skeleton. A mutation in this gene has been shown to result in spondylocostal dysostosis. Multiple transcript variants encoding different isoforms have been found for this gene.
    UniProt
    Q9BYE0
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