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NHLRC1 anticorps

NHLRC1 Reactivité: Humain, Rat, Souris IHC, IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7262557
  • Antigène Voir toutes NHLRC1 Anticorps
    NHLRC1 (NHL Repeat Containing 1 (NHLRC1))
    Reactivité
    • 18
    • 3
    • 1
    • 1
    Humain, Rat, Souris
    Hôte
    • 16
    • 3
    Lapin
    Clonalité
    • 16
    • 3
    Polyclonal
    Conjugué
    • 10
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp NHLRC1 est non-conjugé
    Application
    • 9
    • 9
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human NHLRC1 (NP_940988.2).
    Isotype
    IgG
    Top Product
    Discover our top product NHLRC1 Anticorps primaire
  • Indications d'application
    IHC 1:50-1:200 IF 1:50-1:200
    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
    NHLRC1 (NHL Repeat Containing 1 (NHLRC1))
    Autre désignation
    NHLRC1 (NHLRC1 Produits)
    Synonymes
    anticorps EPM2A, anticorps EPM2B, anticorps MALIN, anticorps bA204B7.2, anticorps AI505271, anticorps B230309E09Rik, anticorps Epm2b, anticorps malin-like, anticorps NHL repeat containing E3 ubiquitin protein ligase 1, anticorps NHL repeat containing 1, anticorps NHLRC1, anticorps Nhlrc1
    Sujet
    The protein encoded by this gene is a single subunit E3 ubiquitin ligase. Laforin is polyubiquitinated by the encoded protein. Defects in this intronless gene lead to an accumulation of laforin and onset of Lafora disease, also known as progressive myoclonic epilepsy type 2 (EPM2).
    ID gène
    378884
    UniProt
    Q6VVB1
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