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MAGEA6 antibody

MAGEA6 Reactivity: Human ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5957147
  • Target See all MAGEA6 Antibodies
    MAGEA6 (Melanoma Antigen Family A, 6 (MAGEA6))
    Reactivity
    • 28
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 28
    Rabbit
    Clonality
    • 28
    Polyclonal
    Conjugate
    • 15
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MAGEA6 antibody is un-conjugated
    Application
    • 19
    • 14
    • 4
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    Specificity
    CT1.6,MAGE6,MAGE3B,MAGE-3b
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human MAGEA6
    Isotype
    IgG
    Top Product
    Discover our top product MAGEA6 Primary Antibody
  • Application Notes
    IHC 1:50-200, ELISA 1:2000-10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.9 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    MAGEA6 (Melanoma Antigen Family A, 6 (MAGEA6))
    Alternative Name
    MAGEA6 (MAGEA6 Products)
    Synonyms
    Mage-a6 antibody, CT1.6 antibody, MAGE-3b antibody, MAGE3B antibody, MAGE6 antibody, melanoma antigen, family A, 6 antibody, MAGE family member A6 antibody, Magea6 antibody, MAGEA6 antibody
    Background
    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.
    NCBI Accession
    NP_005354
    UniProt
    P43360
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