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MAGEA8 anticorps

MAGEA8 Reactivité: Humain ELISA, WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7000757
  • Antigène Voir toutes MAGEA8 Anticorps
    MAGEA8 (Melanoma Antigen Family A, 8 (MAGEA8))
    Reactivité
    • 17
    • 1
    Humain
    Hôte
    • 16
    • 1
    Lapin
    Clonalité
    • 16
    • 1
    Polyclonal
    Conjugué
    • 7
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp MAGEA8 est non-conjugé
    Application
    • 7
    • 6
    • 2
    • 2
    • 1
    • 1
    ELISA, Western Blotting (WB)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human MAGEA8
    Isotype
    IgG
    Top Product
    Discover our top product MAGEA8 Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.4 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    MAGEA8 (Melanoma Antigen Family A, 8 (MAGEA8))
    Autre désignation
    MAGEA8 (MAGEA8 Produits)
    Synonymes
    anticorps Mage-a8, anticorps RGD1565778, anticorps MAGEA8, anticorps CT1.8, anticorps MAGE8, anticorps melanoma antigen, family A, 8, anticorps MAGE family member A8, anticorps Magea8, anticorps MAGEA8
    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. Multiple alternatively spliced variants, encoding the same protein, have been identified.
    Poids moléculaire
    35 kDa
    UniProt
    P43361
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