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MAGE-Like 2 Antikörper (C-Term)

MAGEL2 Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN929381
  • Target Alle MAGE-Like 2 (MAGEL2) Antikörper anzeigen
    MAGE-Like 2 (MAGEL2)
    Bindungsspezifität
    • 15
    • 8
    • 3
    • 1
    C-Term
    Reaktivität
    • 29
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Wirt
    • 29
    Kaninchen
    Klonalität
    • 29
    Polyklonal
    Konjugat
    • 10
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser MAGE-Like 2 Antikörper ist unkonjugiert
    Applikation
    • 13
    • 13
    • 13
    • 7
    • 7
    • 6
    • 3
    • 1
    Western Blotting (WB)
    Aufreinigung
    Purified
    Immunogen
    MAGEL2 antibody was raised in rabbit using the C terminal of MAGEL2 as the immunogen
    Top Product
    Discover our top product MAGEL2 Primärantikörper
  • Applikationshinweise
    WB: 0.2-1 µg/mL
    Optimal conditions should be determined by the investigator.
    Kommentare

    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

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Konzentration
    Lot specific
    Buffer
    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
    Handhabung
    Avoid repeated freeze/thaw cycles.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • Target
    MAGE-Like 2 (MAGEL2)
    Andere Bezeichnung
    MAGEL2 (MAGEL2 Produkte)
    Synonyme
    NDNL1 antikoerper, nM15 antikoerper, MAGEL2 antikoerper, Mage-l2 antikoerper, ns7 antikoerper, MAGE family member L2 antikoerper, melanoma antigen, family L, 2 antikoerper, MAGEL2 antikoerper, Magel2 antikoerper
    Hintergrund
    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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