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MAGEA6 antibody

MAGEA6 Reactivity: Human, Mouse IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7012179
  • Target See all MAGEA6 Antibodies
    MAGEA6 (Melanoma Antigen Family A, 6 (MAGEA6))
    Reactivity
    • 25
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Human, Mouse
    Host
    • 25
    Rabbit
    Clonality
    • 25
    Polyclonal
    Conjugate
    • 12
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MAGEA6 antibody is un-conjugated
    Application
    • 17
    • 13
    • 4
    • 2
    • 1
    Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human MAGEA6 (NP_005354.1).
    Isotype
    IgG
    Top Product
    Discover our top product MAGEA6 Primary Antibody
  • Application Notes
    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
    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.
    Gene ID
    4105
    UniProt
    P43360
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