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Ubiquitin Protein Ligase E3A Recombinant Rabbit mAb

Product Specifications

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]

CAS Number

9000-83-3

Structure Composition

Store at -20°C. Supplied in 50mM Tris-Glycine (pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.

Product Name Alternative

AS; ANCR; E6-AP; HPVE6A; EPVE6AP

Swiss Prot

Q05086

Reactivity

Human, Mouse, Rat

Immunogen

Recombinant protein of human UBE3A

Conjugation

Unconjugated

Applications

WB, ICC/IF, FC, IP

Purity

Affinity Purification

Modification

Unmodification

Molecular Weight

101 kDa

Storage Conditions

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.

Notes

For research use only, not for use in diagnostic procedure.

Specificity

IgG

Applications Notes

Western blot analysis of extracts from 3T3 cells at 1:1000.

Host or Source

Rabbit

Available Sizes

Frequently Asked Questions

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