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, ELISA, IF and IP. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN5698660

Quick Overview for ube3a antibody (ABIN5698660)

Target

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

Reactivity

  • 56
  • 11
  • 8
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 48
  • 8
Rabbit

Clonality

  • 46
  • 10
Polyclonal

Conjugate

  • 30
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ube3a antibody is un-conjugated

Application

  • 32
  • 16
  • 16
  • 13
  • 13
  • 11
  • 9
  • 9
  • 7
  • 5
  • 3
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)
  • Immunogen

    ubiquitin protein ligase E3A

    Isotype

    IgG
  • Application Notes

    WB : 1:500-1:5000,IHC:1:20-1:200,IP:1:200-1:1000,IF:1:10-1:100

    Comment

    mouse brain tissue were subjected to SDS PAGE followed by western blot with FNab09189(UBE3A antibody) at dilution of 1:1000

    Restrictions

    For Research Use only
  • 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.

    Handling Advice

    Avoid repeated freeze / thaw cycles.

    Storage

    -20 °C

    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

    38kDa,Observed 45kDa

    Gene ID

    7337

    UniProt

    Q05086

    Pathways

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