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IDI1 anticorps

IDI1 Reactivité: Humain, Souris WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6292160
  • Antigène Voir toutes IDI1 Anticorps
    IDI1 (Isopentenyl-Diphosphate delta Isomerase 1 (IDI1))
    Reactivité
    • 31
    • 19
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris
    Hôte
    • 27
    • 4
    Lapin
    Clonalité
    • 30
    • 1
    Polyclonal
    Conjugué
    • 17
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp IDI1 est non-conjugé
    Application
    • 31
    • 13
    • 13
    • 7
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human IDI1
    Isotype
    IgG
    Top Product
    Discover our top product IDI1 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
    IDI1 (Isopentenyl-Diphosphate delta Isomerase 1 (IDI1))
    Autre désignation
    IDI1 (IDI1 Produits)
    Synonymes
    anticorps zgc:114138, anticorps 4832416K17Rik, anticorps ipp1, anticorps ippl1, anticorps IPP1, anticorps IPPI1, anticorps isopentenyl-diphosphate delta isomerase 1, anticorps isopentenyl-diphosphate delta isomerase, anticorps isopentenyl-diphosphate delta isomerase 1 L homeolog, anticorps idi1, anticorps Idi1, anticorps idi1.L, anticorps IDI1
    Sujet
    IDI1 encodes a peroxisomally-localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP), which are the substrates for the successive reaction that results in the synthesis of farnesyl diphosphate and, ultimately, cholesterol. It has been shown in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy that there is reduction in IPP isomerase activity.
    Poids moléculaire
    26.319 kDa
    ID gène
    3422
    UniProt
    Q13907
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