Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

ube3a antibody

This Rabbit Polyclonal antibody specifically detects ube3a in WB, IHC and ELISA. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7120486

Quick Overview for ube3a antibody (ABIN7120486)

Target

See all ube3a Antibodies
ube3a (Ubiquitin Protein Ligase E3A (ube3a))

Reactivity

  • 57
  • 11
  • 8
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 51
  • 6
Rabbit

Clonality

  • 49
  • 8
Polyclonal

Conjugate

  • 34
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ube3a antibody is un-conjugated

Application

  • 32
  • 20
  • 17
  • 13
  • 13
  • 10
  • 10
  • 9
  • 7
  • 6
  • 3
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    ubiquitin protein ligase E3A

    Isotype

    IgG
  • Application Notes

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Expiry Date

    12 months
  • Target

    ube3a (Ubiquitin Protein Ligase E3A (ube3a))

    Alternative Name

    UBE3A

    Background

    Synonyms:ANCR, AS, E6 AP, E6AP, E6AP ubiquitin protein ligase, EPVE6AP, FLJ26981, HPVE6A, 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.

    Molecular Weight

    110 kDa

    Gene ID

    7337

    UniProt

    Q05086

    Pathways

    Intracellular Steroid Hormone Receptor Signaling Pathway
You are here:
Chat with us!