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ZBTB20 antibody

ZBTB20 Reactivity: Human, Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7012097
  • Target See all ZBTB20 Antibodies
    ZBTB20 (Zinc Finger and BTB Domain Containing 20 (ZBTB20))
    Reactivity
    • 12
    • 6
    • 5
    • 5
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 12
    • 1
    Rabbit
    Clonality
    • 12
    • 1
    Polyclonal
    Conjugate
    • 13
    This ZBTB20 antibody is un-conjugated
    Application
    • 10
    • 5
    • 4
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human ZBTB20 (NP_056457.3).
    Isotype
    IgG
    Top Product
    Discover our top product ZBTB20 Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    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
    ZBTB20 (Zinc Finger and BTB Domain Containing 20 (ZBTB20))
    Alternative Name
    ZBTB20 (ZBTB20 Products)
    Background
    This gene, which was initially designated as dendritic cell-derived BTB/POZ zinc finger (DPZF), belongs to a family of transcription factors with an N-terminal BTB/POZ domain and a C-terminal DNA-bindng zinc finger domain. The BTB/POZ domain is a hydrophobic region of approximately 120 aa which mediates association with other BTB/POZ domain-containing proteins. This gene acts as a transcriptional repressor and plays a role in many processes including neurogenesis, glucose homeostasis, and postnatal growth. Mutations in this gene have been associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
    Molecular Weight

    Observed_MW: 81 kDa

    Calculated_MW: 73 kDa/81 kDa

    Gene ID
    26137
    UniProt
    Q9HC78
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