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Tat (AA 1-270) antibody

Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6148867
  • Target
    Tat
    Binding Specificity
    • 7
    • 6
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-270
    Reactivity
    • 28
    • 8
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 27
    • 1
    Rabbit
    Clonality
    • 27
    • 1
    Polyclonal
    Conjugate
    • 13
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Un-conjugated
    Application
    • 16
    • 15
    • 10
    • 7
    • 3
    • 1
    • 1
    Western Blotting (WB)
    Sequence
    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
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Polyclonal Antibodies
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-270 of human TAT (NP_000344.1).
    Isotype
    IgG
  • Application Notes
    WB,1:500 - 1:2000
    Comment

    HIGH QUALITY

    Restrictions
    For Research Use only
  • Format
    Liquid
    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
    Tat
    Synonyms
    wu:fb60g09 antibody, zgc:154059 antibody, si:ch211-238a12.1 antibody, tyrosine aminotransferase antibody, TAT antibody, Tat antibody, tat antibody
    Target Type
    Viral Protein
    Background
    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
    Molecular Weight
    50 kDa
    Gene ID
    6898
    UniProt
    P17735
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