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TAT anticorps (AA 169-208)

TAT Reactivité: Humain, Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5647931
  • Antigène Voir toutes TAT Anticorps
    TAT (tyrosine Aminotransferase (TAT))
    Épitope
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 169-208
    Reactivité
    • 14
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 15
    Lapin
    Clonalité
    • 15
    Polyclonal
    Conjugué
    • 10
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp TAT est non-conjugé
    Application
    • 12
    • 12
    • 8
    • 7
    • 3
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Antigen affinity purified
    Immunogène
    Amino acids 169-208 (FSLYKTLAESMGIEVKLYNLLPEKSWEIDLKQLEYLIDEK-human) were used as the immunogen for the TAT antibody.
    Isotype
    IgG
    Top Product
    Discover our top product TAT Anticorps primaire
  • Indications d'application
    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
    Stock
    -20 °C
    Stockage commentaire
    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.
  • Antigène
    TAT (tyrosine Aminotransferase (TAT))
    Autre désignation
    TAT / Tyrosine aminotransferase (TAT Produits)
    Synonymes
    anticorps MGC89628, anticorps wu:fb60g09, anticorps zgc:154059, anticorps si:ch211-238a12.1, anticorps F27C12.23, anticorps F27C12_23, anticorps TAT, anticorps TYROSINE AMINOTRANSFERASE, anticorps tyrosine aminotransferase 3, anticorps tyrosine aminotransferase, anticorps tyrosine aminotransferase 3, anticorps TAT, anticorps Tat, anticorps tat, anticorps TAT3
    Sujet
    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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