HomeProductsUbiquitin Protein Ligase E3A Rabbit pAb
Ubiquitin Protein Ligase E3A Rabbit pAb
Cat Number: DPA02186
Ubiquitin Protein Ligase E3A Rabbit pAb
Applications:
FCICC/IFIPWB
Species Reactivity:
HumanMouseRat
$ 169
/ 50ul
In Stock
50ul100ul
Description
Recommended Dilution
Product Features
Applications
FCICC/IFIPWB
Species Reactivity
HumanMouseRat
Uniprot
Q05086
GeneID
7337
Isotype
IgG
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, Jul 2008]
Calculated molecular weight
101 kDa
MW
101 kDa
Purification method
Affinity Purification
Conjugate
Un-conjugated
Clonality
Polyclonal
Host species
Rabbit
Immunogen
Recombinant protein of human UBE3A
Alias
AS; ANCR; E6-AP; HPVE6A; EPVE6AP
Cat Number: DPA02186
Ubiquitin Protein Ligase E3A Rabbit pAb
Applications:
FCICC/IFIPWB
Species Reactivity:
HumanMouseRat
$ 169
/ 50ul
In Stock
50ul100ul
Description
Recommended Dilution
Product Features
Applications
FCICC/IFIPWB
Species Reactivity
HumanMouseRat
Uniprot
Q05086
GeneID
7337
Isotype
IgG
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, Jul 2008]