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MAGE-Like 2 antibody (C-Term)

MAGEL2 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN929381
  • Target See all MAGE-Like 2 (MAGEL2) Antibodies
    MAGE-Like 2 (MAGEL2)
    Binding Specificity
    • 15
    • 7
    • 3
    • 1
    C-Term
    Reactivity
    • 33
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 33
    Rabbit
    Clonality
    • 33
    Polyclonal
    Conjugate
    • 8
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MAGE-Like 2 antibody is un-conjugated
    Application
    • 13
    • 13
    • 11
    • 6
    • 6
    • 5
    • 3
    • 1
    Western Blotting (WB)
    Purification
    Purified
    Immunogen
    MAGEL2 antibody was raised in rabbit using the C terminal of MAGEL2 as the immunogen
    Top Product
    Discover our top product MAGEL2 Primary Antibody
  • Application Notes
    WB: 0.2-1 µg/mL
    Optimal conditions should be determined by the investigator.
    Comment

    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.
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • Target
    MAGE-Like 2 (MAGEL2)
    Alternative Name
    MAGEL2 (MAGEL2 Products)
    Synonyms
    NDNL1 antibody, nM15 antibody, MAGEL2 antibody, Mage-l2 antibody, ns7 antibody, MAGE family member L2 antibody, melanoma antigen, family L, 2 antibody, MAGEL2 antibody, Magel2 antibody
    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. Synonyms: Polyclonal MAGEL2 antibody, Anti-MAGEL2 antibody, MAGE-like 2 antibody, NDNL1 antibody, nM15 antibody.
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