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BAZ1B antibody

BAZ1B Reactivity: Human, Mouse, Rat WB, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6572045
  • Target See all BAZ1B Antibodies
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    Reactivity
    • 54
    • 14
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    Human, Mouse, Rat
    Host
    • 49
    • 5
    Rabbit
    Clonality
    • 42
    • 12
    Polyclonal
    Conjugate
    • 22
    • 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
    • 22
    • 16
    • 14
    • 13
    • 7
    • 6
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human BAZ1B
    Isotype
    IgG
    Top Product
    Discover our top product BAZ1B Primary Antibody
  • Application Notes
    WB 1:500 - 1:2000 IHC 1:50 - 1:200
    Restrictions
    For Research Use only
  • Concentration
    1 mg/mL
    Buffer
    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    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
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    Alternative Name
    BAZ1B (BAZ1B Products)
    Background

    Synonyms: Bromodomain Adjacent To Zinc Finger Domain 1B,Williams-Beuren Syndrome Chromosomal Region 10 Protein,Williams-Beuren Syndrome Chromosomal Region 9 Protein,Williams Syndrome Transcription Factor,Transcription Factor WSTF,EC 2.7.10.2,WBSCR10,WBSCR9.

    Background: This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.

    Molecular Weight

    Observed_MW: 190kDa

    Calculated_MW: 170kDa

    Gene ID
    9031
    UniProt
    Q9UIG0
    Pathways
    Nuclear Hormone Receptor Binding, Chromatin Binding
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