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MAGE-Like 2 anticorps

MAGEL2 Reactivité: Humain ELISA, WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7191360
  • Antigène Voir toutes MAGE-Like 2 (MAGEL2) Anticorps
    MAGE-Like 2 (MAGEL2)
    Reactivité
    • 28
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 28
    Lapin
    Clonalité
    • 28
    Polyclonal
    Conjugué
    • 9
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp MAGE-Like 2 est non-conjugé
    Application
    • 13
    • 13
    • 12
    • 7
    • 6
    • 6
    • 3
    • 1
    ELISA, Western Blotting (WB)
     Réactivité croisée
    Humain
    Purification
    Antigen affinity purification
    Immunogène
    Synthetic peptide of Human MAGEL2
    Isotype
    IgG
    Top Product
    Discover our top product MAGEL2 Anticorps primaire
  • Indications d'application
    ELISA:1:1000-1:2000, WB:1:200-1:1000,
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    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,-80 °C
    Stockage commentaire
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Antigène
    MAGE-Like 2 (MAGEL2)
    Autre désignation
    MAGEL2 (MAGEL2 Produits)
    Synonymes
    anticorps NDNL1, anticorps nM15, anticorps MAGEL2, anticorps Mage-l2, anticorps ns7, anticorps MAGE family member L2, anticorps melanoma antigen, family L, 2, anticorps MAGEL2, anticorps Magel2
    Sujet

    Background: Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS.

    Aliases: MAGEL2 antibody, NDNL1 antibody, MAGE-like protein 2 antibody, Necdin-like protein 1 antibody, Protein nM15 antibody

    UniProt
    Q9UJ55
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