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MAGEA3 antibody

MAGEA3 Reactivity: Human WB, ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2426633
  • Target See all MAGEA3 Antibodies
    MAGEA3 (Melanoma Antigen Family A, 3 (MAGEA3))
    Reactivity
    • 42
    • 1
    • 1
    Human
    Host
    • 29
    • 12
    • 1
    Rabbit
    Clonality
    • 30
    • 11
    • 1
    Polyclonal
    Conjugate
    • 27
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MAGEA3 antibody is un-conjugated
    Application
    • 31
    • 20
    • 16
    • 12
    • 5
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human MAGEA3
    Isotype
    IgG
    Top Product
    Discover our top product MAGEA3 Primary Antibody
  • Application Notes
    WB 1:500-1:2000, IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Handling Advice
    Avoid freeze / thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    MAGEA3 (Melanoma Antigen Family A, 3 (MAGEA3))
    Alternative Name
    MAGEA3 (MAGEA3 Products)
    Synonyms
    CT1.3 antibody, HIP8 antibody, HYPD antibody, MAGE3 antibody, MAGEA6 antibody, Mage-a3 antibody, MAGEA3 antibody, MAGE family member A3 antibody, melanoma antigen, family A, 3 antibody, melanoma antigen family A, 3 antibody, MAGEA3 antibody, Magea3 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.
    Molecular Weight
    Calculated MW: 35 kDa
    NCBI Accession
    NP_005353
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