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T-Box 22 antibody

TBX22 Reactivity: Human, Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5965981
  • Target See all T-Box 22 (TBX22) Antibodies
    T-Box 22 (TBX22)
    Reactivity
    • 24
    • 19
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    Human, Mouse, Rat
    Host
    • 37
    • 3
    Rabbit
    Clonality
    • 37
    • 3
    Polyclonal
    Conjugate
    • 19
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This T-Box 22 antibody is un-conjugated
    Application
    • 32
    • 13
    • 13
    • 12
    • 4
    • 4
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human TBX22
    Isotype
    IgG
    Top Product
    Discover our top product TBX22 Primary Antibody
  • Application Notes
    WB 1:500 - 1:2000
    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
    T-Box 22 (TBX22)
    Alternative Name
    TBX22 (TBX22 Products)
    Synonyms
    TBX22 antibody, ABERS antibody, CLPA antibody, CPX antibody, TBXX antibody, dJ795G23.1 antibody, D230020M15Rik antibody, Tbx 22 antibody, T-box 22 antibody, TBX22 antibody, tbx22 antibody, Tbx22 antibody
    Background

    Synonyms: ABERS,CLPA,CPX,D230020M15Rik,dJ795G23.1,T box 22,T box protein 22,T box transcription factor TBX22,T-box protein 22,T-box transcription factor TBX22,Tbx22,TBX22,TBXX

    Background: This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene have been associated with the inherited X-linked disorder, Cleft palate with ankyloglossia, and it is believed to play a major role in human palatogenesis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

    Molecular Weight

    Observed_MW: 50kDa

    Calculated_MW: 44kDa/57kDa

    Gene ID
    50945
    UniProt
    Q9Y458
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