|Full Name||ubiquitin protein ligase E3A|
|Product Description||Rabbit Polyclonal antibody to UBE3A (ubiquitin protein ligase E3A)|
|Background||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]|
|Synonyms||ANCR Antibody, HPVE6A Antibody, EPVE6AP Antibody, ubiquitin protein ligase E3A Antibody, E6-AP Antibody, AS Antibody|
|Cellular Localization||Nucleus |
|Immunogen||Recombinant protein encompassing a sequence within the center region of human UBE3A. The exact sequence is proprietary.|
|Species Reactivity||Human, Mouse|
|Predicted Cross Reactivity species Predicted cross-reactivity:|
Predicted cross-reactivity is based on sequence homology, with greater than 80% immunogen sequence identity considered positive.
Please note that we are only able to guarantee products to work in applications and species in which they have been tested.
|Rat, Xenopus laevis, Pig, Rhesus Monkey, Bovine|
|Predict Reactivity Note||Rat (92%), Xenopus laevis (86%), Pig (95%), Rhesus Monkey (99%), Bovine (95%)|