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MAGE-Like 2 anticorps (C-Term)

L’anticorps Lapin Polyclonal anti-MAGE-Like 2 a été validé pour WB. Il convient pour détecter MAGE-Like 2 dans des échantillons de Humain.
N° du produit ABIN929381

Aperçu rapide pour MAGE-Like 2 anticorps (C-Term) (ABIN929381)

Antigène

Voir toutes MAGE-Like 2 (MAGEL2) Anticorps
MAGE-Like 2 (MAGEL2)

Reactivité

  • 34
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 34
  • 1
Lapin

Clonalité

  • 34
  • 1
Polyclonal

Conjugué

  • 10
  • 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
  • 12
  • 8
  • 8
  • 5
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Épitope

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

    Purification

    Purified

    Immunogène

    MAGEL2 antibody was raised in rabbit using the C terminal of MAGEL2 as the immunogen
  • Indications d'application

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

    Commentaires

    MAGEL2 Blocking Peptide, (ABIN5614639), 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

    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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