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CHD7 antibody (AA 2025-2075)

This Rabbit Polyclonal antibody specifically detects CHD7 in IP. It exhibits reactivity toward Human.
Catalog No. ABIN7451215
$538.15
Plus shipping costs $50.00
Shipping to: United States
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Quick Overview for CHD7 antibody (AA 2025-2075) (ABIN7451215)

Target

See all CHD7 Antibodies
CHD7 (Chromodomain Helicase DNA Binding Protein 7 (CHD7))

Reactivity

  • 7
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 7
  • 1
Rabbit

Clonality

  • 8
Polyclonal

Conjugate

  • 8
This CHD7 antibody is un-conjugated

Application

  • 6
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Immunoprecipitation (IP)
  • Binding Specificity

    • 2
    • 2
    • 2
    • 1
    • 1
    AA 2025-2075

    Purpose

    Rabbit anti-CHD7 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 2025 and 2075

    Isotype

    IgG
  • 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

    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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