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MAGE-Like 2 anticorps

MAGEL2 Reactivité: Humain, Souris, Rat ELISA, WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2433343
  • Antigène Voir toutes MAGE-Like 2 (MAGEL2) Anticorps
    MAGE-Like 2 (MAGEL2)
    Reactivité
    • 32
    • 2
    • 2
    • 2
    • 2
    • 1
    Humain, Souris, Rat
    Hôte
    • 32
    Lapin
    Clonalité
    • 32
    Polyclonal
    Conjugué
    • 7
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp MAGE-Like 2 est non-conjugé
    Application
    • 13
    • 13
    • 10
    • 6
    • 5
    • 5
    • 3
    • 1
    ELISA, Western Blotting (WB)
    Purification
    Antigen affinity purification
    Immunogène
    Synthetic peptide of human MAGEL2
    Isotype
    IgG
    Top Product
    Discover our top product MAGEL2 Anticorps primaire
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Conseil sur la manipulation
    Avoid freeze / thaw cycles.
    Stock
    -20 °C/-80 °C
    Stockage commentaire
    Store at -20°C (regular) and -80°C (long term).
  • 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
    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.
    Synonyms: PWLS, nM15, NDNL1
    Poids moléculaire
    Calculated MW: 59 kDa
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