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Tat (AA 1-270) anticorps

Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6148867
  • Antigène
    Tat
    Épitope
    • 7
    • 6
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-270
    Reactivité
    • 28
    • 8
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 27
    • 1
    Lapin
    Clonalité
    • 27
    • 1
    Polyclonal
    Conjugué
    • 13
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Inconjugué
    Application
    • 16
    • 15
    • 10
    • 7
    • 3
    • 1
    • 1
    Western Blotting (WB)
    Séquence
    MDPYMIQMSS KGNLPSILDV HVNVGGRSSV PGKMKGRKAR WSVRPSDMAK KTFNPIRAIV DNMKVKPNPN KTMISLSIGD PTVFGNLPTD PEVTQAMKDA LDSGKYNGYA PSIGFLSSRE EIASYYHCPE APLEAKDVIL TSGCSQAIDL CLAVLANPGQ NILVPRPGFS LYKTLAESMG IEVKLYNLLP EKSWEIDLKQ LEYLIDEKTA CLIVNNPSNP CGSVFSKRHL QKILAVAARQ CVPILADEIY GDMVFSDCKY EPLATLSTDV
     Réactivité croisée
    Humain, Souris, Rat
    Attributs du produit
    Polyclonal Antibodies
    Immunogène
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-270 of human TAT (NP_000344.1).
    Isotype
    IgG
  • Indications d'application
    WB,1:500 - 1:2000
    Commentaires

    HIGH QUALITY

    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    Tat
    Synonymes
    anticorps wu:fb60g09, anticorps zgc:154059, anticorps si:ch211-238a12.1, anticorps tyrosine aminotransferase, anticorps TAT, anticorps Tat, anticorps tat
    Classe de substances
    Viral Protein
    Sujet
    This nuclear gene encodes a 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.,TAT,Cancer,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,TAT
    Poids moléculaire
    50 kDa
    ID gène
    6898
    UniProt
    P17735
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