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CHD7 antibody (AA 2025-2075)

CHD7 Reactivity: Human IP Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7451215
  • Target See all CHD7 Antibodies
    CHD7 (Chromodomain Helicase DNA Binding Protein 7 (CHD7))
    Binding Specificity
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 2025-2075
    Reactivity
    • 9
    • 3
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 7
    • 1
    • 1
    Rabbit
    Clonality
    • 9
    Polyclonal
    Conjugate
    • 9
    This CHD7 antibody is un-conjugated
    Application
    • 8
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Immunoprecipitation (IP)
    Purpose
    Rabbit anti-CHD7 Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogen
    between AA 2025 and 2075
    Isotype
    IgG
    Top Product
    Discover our top product CHD7 Primary Antibody
  • Application Notes

    IP: 2 - 10 μg/mg lysate

    WB: Not recommended. Use rabbit anti-CHD7 antibody ABIN7453314.

    Restrictions
    For Research Use only
  • Concentration
    1000 μg/mL
    Buffer
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
    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
    Expiry Date
    12 months
  • Target
    CHD7 (Chromodomain Helicase DNA Binding Protein 7 (CHD7))
    Alternative Name
    CHD7 (CHD7 Products)
    Background
    Background: CHD7 is a member of the CHD (chromodomain-helicase-DNA-binding) family of proteins that interacts with nucleosomes and plays a role in chromatin remodeling to modulate transcription. The members of the CHD family of proteins possess 3 common structural and functional domains: a chromodomain (chromatin organization modifier), an SNF2-like helicase/ATPase domain, and a C-terminal DNA-binding domain. CHD7 is implicated to play a role in development. Mutations in CHD7 are associated with CHARGE syndrome, a multi-symptom syndrome characterized by congenital anomalies and malformations of the heart, inner ear, retina, and palate.
    Gene ID
    55636
    NCBI Accession
    NP_060250
    UniProt
    Q9P2D1
    Pathways
    Sensory Perception of Sound, Chromatin Binding
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