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QPRT anticorps

QPRT Reactivité: Humain, Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6290813
  • Antigène Voir toutes QPRT Anticorps
    QPRT (Quinolinate Phosphoribosyltransferase (QPRT))
    Reactivité
    Humain, Souris, Rat
    Hôte
    • 25
    • 5
    Lapin
    Clonalité
    • 28
    • 2
    Polyclonal
    Conjugué
    • 13
    • 4
    • 3
    • 3
    • 3
    • 3
    • 1
    Cet anticorp QPRT est non-conjugé
    Application
    • 21
    • 19
    • 18
    • 4
    • 4
    • 3
    • 3
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human QPRT
    Isotype
    IgG
    Top Product
    Discover our top product QPRT 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
    QPRT (Quinolinate Phosphoribosyltransferase (QPRT))
    Autre désignation
    QPRT (QPRT Produits)
    Synonymes
    anticorps ECK0108, anticorps JW0105, anticorps VF2184, anticorps QPRTase, anticorps 2410027J01Rik, anticorps AI647766, anticorps quinolinate phosphoribosyltransferase, anticorps nicotinate-nucleotide pyrophosphorylase, anticorps nicotinate-nucleotide diphosphorylase, anticorps carboxylating, anticorps ECs0113, anticorps nadC, anticorps VP2522, anticorps STY0167, anticorps BJE04_RS13210, anticorps QPRT, anticorps Qprt
    Sujet
    This gene encodes a key enzyme in catabolism of quinolinate, an intermediate in the tryptophan-nicotinamide adenine dinucleotide pathway. Quinolinate acts as a most potent endogenous exitotoxin to neurons. Elevation of quinolinate levels in the brain has been linked to the pathogenesis of neurodegenerative disorders such as epilepsy, Alzheimer's disease, and Huntington's disease. Alternative splicing results in multiple transcript variants.
    Poids moléculaire
    30.846 kDa
    ID gène
    23475
    UniProt
    Q15274
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