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OCRL anticorps

OCRL Reactivité: Humain, Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7264779
  • Antigène Voir toutes OCRL Anticorps
    OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))
    Reactivité
    • 27
    • 11
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 21
    • 6
    Lapin
    Clonalité
    • 24
    • 3
    Polyclonal
    Conjugué
    • 16
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp OCRL est non-conjugé
    Application
    • 15
    • 11
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human OCRL (NP_001578.2).
    Isotype
    IgG
    Top Product
    Discover our top product OCRL Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    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
    OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))
    Autre désignation
    OCRL (OCRL Produits)
    Synonymes
    anticorps OCRL, anticorps wu:fi09g03, anticorps zgc:152864, anticorps locr, anticorps nphl2, anticorps ocrl1, anticorps inpp5f, anticorps INPP5F, anticorps LOCR, anticorps NPHL2, anticorps OCRL-1, anticorps OCRL1, anticorps 9530014D17Rik, anticorps BB143339, anticorps OCRL, inositol polyphosphate-5-phosphatase, anticorps phosphatidylinositol polyphosphate 5-phosphatase, anticorps oculocerebrorenal syndrome of Lowe, anticorps Ocrl, anticorps NAEGRDRAFT_58601, anticorps OCRL, anticorps ocrl
    Sujet
    This gene encodes an inositol polyphosphate 5-phosphatase. This protein is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans-Golgi network, clathrin-coated vesicles and, endosomes and the plasma membrane. This protein may also play a role in primary cilium formation. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. Alternate splicing results in multiple transcript variants.
    Poids moléculaire

    Observed_MW: 110 kDa

    Calculated_MW: 103 kDa/104 kDa

    ID gène
    4952
    UniProt
    Q01968
    Pathways
    Inositol Metabolic Process
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