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MAGEA6 anticorps

MAGEA6 Reactivité: Humain, Souris IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6571579
  • Antigène Voir toutes MAGEA6 Anticorps
    MAGEA6 (Melanoma Antigen Family A, 6 (MAGEA6))
    Reactivité
    • 28
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    Humain, Souris
    Hôte
    • 28
    Lapin
    Clonalité
    • 28
    Polyclonal
    Conjugué
    • 15
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp MAGEA6 est non-conjugé
    Application
    • 19
    • 14
    • 4
    • 3
    • 1
    Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human MAGEA6 (NP_005354.1).
    Isotype
    IgG
    Top Product
    Discover our top product MAGEA6 Anticorps primaire
  • Indications d'application
    IF 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    MAGEA6 (Melanoma Antigen Family A, 6 (MAGEA6))
    Autre désignation
    MAGEA6 (MAGEA6 Produits)
    Synonymes
    anticorps Mage-a6, anticorps CT1.6, anticorps MAGE-3b, anticorps MAGE3B, anticorps MAGE6, anticorps melanoma antigen, family A, 6, anticorps MAGE family member A6, anticorps Magea6, anticorps MAGEA6
    Sujet
    This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80 % sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Alternative splicing results in multiple transcript variants.
    Poids moléculaire

    Observed_MW: 35kDa

    Calculated_MW: 34kDa

    ID gène
    4105
    UniProt
    P43360
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