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BAZ1B antibody (AA 1-50)

BAZ1B Reactivity: Human WB, IP, IHC (fp) Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7453893
  • Target See all BAZ1B Antibodies
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    Binding Specificity
    • 15
    • 9
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 1-50
    Reactivity
    • 53
    • 14
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    Human
    Host
    • 48
    • 5
    Rabbit
    Clonality
    • 41
    • 12
    Polyclonal
    Conjugate
    • 21
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This BAZ1B antibody is un-conjugated
    Application
    • 21
    • 16
    • 14
    • 13
    • 7
    • 6
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
    Purpose
    Rabbit anti-WSTF Antibody, Affinity Purified
    Predicted Reactivity
    Mouse
    Purification
    Affinity Purified
    Immunogen
    between AA 1 and 50
    Isotype
    IgG
    Top Product
    Discover our top product BAZ1B Primary Antibody
  • Application Notes

    IHC: 1:100 to 1:500. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: 2 - 10 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions
    For Research Use only
  • Concentration
    200 μg/mL
    Buffer
    Tris-buffered Saline containing 0.1 % BSA and 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
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    Alternative Name
    WSTF (BAZ1B Products)
    Background
    Background: Williams Syndrome transcription factor (WSTF) gene is one of multiple genes deleted in Williams-Beuren syndrome (WS). WSTF associates with the ISWI-type ATPase SNF2H to form the WICH complex. This complex remodels chromatin at replication foci by mobilizing nucleosomes to allow access of factors to newly replicated DNA for restoration of the epigenetic state.
    Gene ID
    9031
    NCBI Accession
    NP_115784
    UniProt
    Q9UIG0
    Pathways
    Nuclear Hormone Receptor Binding, Chromatin Binding
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