Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

ube3a anticorps

Cet anticorps Souris Monoclonal détecte spécifiquement ube3a dans IF et FACS. Il présente une réactivité avec des échantillons de Humain.
N° du produit ABIN7863487
639,45 €
Plus frais de livraison 40,00 € et TVA
Destination: France
Envoi sous 6 à 10 jours ouvrables

Aperçu rapide pour ube3a anticorps (ABIN7863487)

Antigène

Voir toutes ube3a Anticorps
ube3a (Ubiquitin Protein Ligase E3A (ube3a))

Reactivité

  • 65
  • 13
  • 9
  • 6
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 52
  • 13
Souris

Clonalité

  • 48
  • 17
Monoclonal

Conjugué

  • 39
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ube3a est non-conjugé

Application

  • 39
  • 17
  • 16
  • 16
  • 16
  • 13
  • 13
  • 10
  • 7
  • 4
  • 3
  • 1
Immunofluorescence (IF), Flow Cytometry (FACS)

Clone

PCRP-UBE3A-1A2
  • Fonction

    UBE3A / E6-AP Antibody

    Specificité

    E6-associating protein (E6-AP), also designated ubiquitin protein ligase E3A(UBE3A), is a component of the ubiquitin-mediated proteolytic pathway thatselectively targets proteins for degradation by the 26S Proteasome. Ubiquitin(Ub) is directly conjugated to protein substrates by the transfer of Ub from anE2 ubiquitin conjugating enzyme to the target protein. This conjugation is facil-itated by the enzymatic activity of E3 ubiquitin ligase family members such asE6-AP. Several substrates of E6-AP have been identified and include the tumorsuppressor protein p53 and the mammalian homolog of Rad23, HHR23A.Previous studies have indicated that E6-AP associates with the humanpapillomavirus E6 oncogene, which forms a complex with p53 and therebypotentiates E6-AP mediated ubiquitination of p53. Genetic mutations thatimpair E6-AP activity result in the accumulation of p53 in the cytoplasm, andin many instances, these mutations are associated with the development ofthe rare neurodevelopmental disorder Angelman syndrome (AS), which ischaracterized by severe motor dysfunction and mental retardation.

    Purification

    200ug/ml of Ab purified from Bioreactor Concentrate by Protein A/G.

    Immunogène

    Recombinant full-length human UBE3A protein

    Isotype

    IgG1
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Concentration

    200 μg/mL

    Buffer

    Prepared in 10 mM PBS with 0.05 % BSA & 0.05 % azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    4 °C

    Stockage commentaire

    Antibody with azide - store at 2 to 8 °C. Antibody without azide - store at -20 to -80 °C. Antibody is stable for 24 months. Non-hazardous. No MSDS required.

    Date de péremption

    24 months
  • Antigène

    ube3a (Ubiquitin Protein Ligase E3A (ube3a))

    Autre désignation

    UBE3A

    Sujet

    ANCR, Angelman syndrome (AS), CTCL tumor antigen se37-2, E6AP ubiquitin protein ligase, EPVE6AP, FLJ26981, HECT-type ubiquitin transferase E3A, Human papilloma virus E6 associated protein Angelman syndrome, HPVE6A, NY REN 54 antigen, Oncogenic protein associated protein E6AP, Renal carcinoma antigen NY REN 54,

    HeLa cells.

    Poids moléculaire

    100kDa

    ID gène

    7337, 598862

    UniProt

    Q05086

    Pathways

    Intracellular Steroid Hormone Receptor Signaling Pathway
Vous êtes ici:
Chat with us!