Melanoma Antigen Family A5 (MAGEA5)

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MAGE5; CT1.5; Cancer/Testis Antigen Family 1, Member 5; Melanoma-Associated Antigen 5

Melanoma Antigen Family A5 (MAGEA5)
MAGEA5 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. This MAGEA gene encodes a protein that is C-terminally truncated compared to other family members, and this gene can be alternatively interpreted to be a pseudogene. The protein is represented in this Entrez Gene record in accordance with the assumed protein-coding status defined in the literature.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Melanoma Antigen Family A5 (MAGEA5) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Melanoma Antigen Family A5 (MAGEA5) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Melanoma Antigen Family A5 (MAGEA5) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Melanoma Antigen Family A5 (MAGEA5) CLIA Kit Customized Service Offer
n/a ELISA Kit for Melanoma Antigen Family A5 (MAGEA5) ELISA Kit Customized Service Offer
  1. "Structure, chromosomal localization, and expression of 12 genes of the MAGE family."Immunogenetics 40:360-369(1994) [PubMed] [Europe PMC] [Abstract]
  2. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  3. "MAGE-A, mMage-b, and MAGE-C proteins form complexes with KAP1 and suppress p53-dependent apoptosis in MAGE-positive cell lines."Cancer Res. 67:9954-9962(2007) [PubMed] [Europe PMC] [Abstract]