DUX4 is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length; a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that contains two homeoboxes; the repeat-array and ORF is conserved in other mammals.
There was no evidence for transcription from standard cDNA libraries however RTPCR and in-vitro expression experiments indicate that the ORF is transcribed and the encoded protein has been reported to function as a transcriptional activator of paired-like homeodomain transcription factor 1 (PITX1). Contraction of the microsatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD).
Organism species: Homo sapiens (Human)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant Double Homeobox Protein 4 (DUX4) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to Double Homeobox Protein 4 (DUX4) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to Double Homeobox Protein 4 (DUX4) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for Double Homeobox Protein 4 (DUX4) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for Double Homeobox Protein 4 (DUX4) | ELISA Kit Customized Service Offer |
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- "Defective regulation of microRNA target genes in myoblasts from facioscapulohumeral dystrophy patients."J. Biol. Chem. 288:34989-35002(2013) [PubMed] [Europe PMC] [Abstract]