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MAGE-Like 2 Antikörper (C-Term)

Der Kaninchen Polyklonal Anti-MAGE-Like 2-Antikörper wurde für WB validiert. Er ist geeignet, MAGE-Like 2 in Proben von Human zu detektieren.
Produktnummer ABIN929381

Kurzübersicht für MAGE-Like 2 Antikörper (C-Term) (ABIN929381)

Target

Alle MAGE-Like 2 (MAGEL2) Antikörper anzeigen
MAGE-Like 2 (MAGEL2)

Reaktivität

  • 34
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 34
  • 2
Kaninchen

Klonalität

  • 34
  • 2
Polyklonal

Konjugat

  • 11
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser MAGE-Like 2 Antikörper ist unkonjugiert

Applikation

  • 13
  • 13
  • 12
  • 9
  • 9
  • 5
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 15
    • 7
    • 3
    • 1
    • 1
    C-Term

    Aufreinigung

    Purified

    Immunogen

    MAGEL2 antibody was raised in rabbit using the C terminal of MAGEL2 as the immunogen
  • Applikationshinweise

    WB: 0.2-1 µg/mL
    Optimal conditions should be determined by the investigator.

    Kommentare

    MAGEL2 Blocking Peptide, (ABIN5614639), 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

    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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