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TAT Antikörper (AA 169-208)

TAT Reaktivität: Human, Maus, Ratte WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN5647931
  • Target Alle TAT Antikörper anzeigen
    TAT (tyrosine Aminotransferase (TAT))
    Bindungsspezifität
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 169-208
    Reaktivität
    • 14
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 15
    Kaninchen
    Klonalität
    • 15
    Polyklonal
    Konjugat
    • 10
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser TAT Antikörper ist unkonjugiert
    Applikation
    • 12
    • 12
    • 8
    • 7
    • 3
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Aufreinigung
    Antigen affinity purified
    Immunogen
    Amino acids 169-208 (FSLYKTLAESMGIEVKLYNLLPEKSWEIDLKQLEYLIDEK-human) were used as the immunogen for the TAT antibody.
    Isotyp
    IgG
    Top Product
    Discover our top product TAT Primärantikörper
  • Applikationshinweise
    Optimal dilution of the TAT antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Buffer
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    Lagerung
    -20 °C
    Informationen zur Lagerung
    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))
    Andere Bezeichnung
    TAT / Tyrosine aminotransferase (TAT Produkte)
    Synonyme
    MGC89628 antikoerper, wu:fb60g09 antikoerper, zgc:154059 antikoerper, si:ch211-238a12.1 antikoerper, F27C12.23 antikoerper, F27C12_23 antikoerper, TAT antikoerper, TYROSINE AMINOTRANSFERASE antikoerper, tyrosine aminotransferase 3 antikoerper, tyrosine aminotransferase antikoerper, tyrosine aminotransferase 3 antikoerper, TAT antikoerper, Tat antikoerper, tat antikoerper, TAT3 antikoerper
    Hintergrund
    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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