E6AP/UBE3A Antibody (3E5)

This product is produced by and distributed for Abnova, a company based in Taiwan.

This gene encodes an E3 ubiquitin-protein ligase, part of the ubiquitin protein degradation system. This imprinted gene is maternally expressed in brain and biallelically expressed in other tissues. Maternally inherited deletion of this gene causes Angelman Syndrome, characterized by severe motor and intellectual retardation, ataxia, hypotonia, epilepsy, absence of speech, and characteristic facies. The protein also interacts with the E6 protein of human papillomavirus types 16 and 18, resulting in ubiquitination and proteolysis of tumor protein p53. Alternative splicing of this gene results in three transcript variants encoding three isoforms with different N-termini. Additional transcript variants have been described, but their full length nature has not been determined. [provided by RefSeq]

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Array H00007337-M02

• E6AP/UBE3A Antibodies
• E6AP/UBE3A ELISA Kits
• E6AP/UBE3A Lysate
• E6AP/UBE3A Proteins
• E6AP/UBE3A Proteins and Enzyme