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TAT antibody (AA 169-208)

TAT Reactivity: Human, Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5647931
  • Target See all TAT Antibodies
    TAT (tyrosine Aminotransferase (TAT))
    Binding Specificity
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 169-208
    Reactivity
    • 14
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 15
    Rabbit
    Clonality
    • 15
    Polyclonal
    Conjugate
    • 10
    • 1
    • 1
    • 1
    • 1
    • 1
    This TAT antibody is un-conjugated
    Application
    • 12
    • 12
    • 8
    • 7
    • 3
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Antigen affinity purified
    Immunogen
    Amino acids 169-208 (FSLYKTLAESMGIEVKLYNLLPEKSWEIDLKQLEYLIDEK-human) were used as the immunogen for the TAT antibody.
    Isotype
    IgG
    Top Product
    Discover our top product TAT Primary Antibody
  • Application Notes
    Optimal dilution of the TAT antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL
    Restrictions
    For Research Use only
  • Buffer
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    Storage
    -20 °C
    Storage Comment
    After reconstitution, the TAT antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target
    TAT (tyrosine Aminotransferase (TAT))
    Alternative Name
    TAT / Tyrosine aminotransferase (TAT Products)
    Synonyms
    MGC89628 antibody, wu:fb60g09 antibody, zgc:154059 antibody, si:ch211-238a12.1 antibody, F27C12.23 antibody, F27C12_23 antibody, TAT antibody, TYROSINE AMINOTRANSFERASE antibody, tyrosine aminotransferase 3 antibody, tyrosine aminotransferase antibody, tyrosine aminotransferase 3 antibody, TAT antibody, Tat antibody, tat antibody, TAT3 antibody
    Background
    The nuclear gene TAT encodes the mitochondrial protein Tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X-linked.
    UniProt
    P17735
    Pathways
    Response to Water Deprivation
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