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TTPA anticorps

TTPA Reactivité: Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6293751
  • Antigène Voir toutes TTPA Anticorps
    TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))
    Reactivité
    • 12
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Souris, Rat
    Hôte
    • 12
    • 1
    Lapin
    Clonalité
    • 12
    • 1
    Polyclonal
    Conjugué
    • 8
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp TTPA est non-conjugé
    Application
    • 12
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human TTPA
    Isotype
    IgG
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    Discover our top product TTPA Anticorps primaire
  • Indications d'application
    WB 1:500 - 1:2000
    Restrictions
    For Research Use only
  • 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 -20C. Avoid freeze / thaw cycles.
  • Antigène
    TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))
    Autre désignation
    TTPA (TTPA Produits)
    Synonymes
    anticorps ATTP, anticorps AVED, anticorps TTP1, anticorps alphaTTP, anticorps TTP, anticorps alpha-TTP, anticorps alpha tocopherol transfer protein, anticorps tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency), anticorps tocopherol (alpha) transfer protein, anticorps TTPA, anticorps ttpa, anticorps Ttpa
    Sujet
    This gene encodes a soluble protein that binds alpha-trocopherol, a form of vitamin E, with high selectivity and affinity. This protein plays an important role in regulating vitamin E levels in the body by transporting vitamin E between membrane vesicles and facilitating the secretion of vitamin E from hepatocytes to circulating lipoproteins. Mutations in this gene cause hereditary vitamin E deficiency (ataxia with vitamin E deficiency, AVED) and retinitis pigmentosa.
    Poids moléculaire
    31.75 kDa
    ID gène
    7274
    UniProt
    P49638
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