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MAGE-Like 2 anticorps (C-Term)

MAGEL2 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN929381
  • Antigène Voir toutes MAGE-Like 2 (MAGEL2) Anticorps
    MAGE-Like 2 (MAGEL2)
    Épitope
    • 15
    • 8
    • 3
    • 1
    C-Term
    Reactivité
    • 29
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 29
    Lapin
    Clonalité
    • 29
    Polyclonal
    Conjugué
    • 10
    • 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
    • 13
    • 7
    • 7
    • 6
    • 3
    • 1
    Western Blotting (WB)
    Purification
    Purified
    Immunogène
    MAGEL2 antibody was raised in rabbit using the C terminal of MAGEL2 as the immunogen
    Top Product
    Discover our top product MAGEL2 Anticorps primaire
  • Indications d'application
    WB: 0.2-1 µg/mL
    Optimal conditions should be determined by the investigator.
    Commentaires

    MAGEL2 Blocking Peptide, catalog no. 33R-6559, is also available for use as a blocking control in assays to test for specificity of this MAGEL2 antibody

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Concentration
    Lot specific
    Buffer
    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
    Conseil sur la manipulation
    Avoid repeated freeze/thaw cycles.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • 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: Polyclonal MAGEL2 antibody, Anti-MAGEL2 antibody, MAGE-like 2 antibody, NDNL1 antibody, nM15 antibody.
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