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ube3a Antikörper

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch ube3a in WB, IHC und ELISA. Er zeigt eine Reaktivität gegenüber Human, Maus und Ratte.
Produktnummer ABIN7120486

Kurzübersicht für ube3a Antikörper (ABIN7120486)

Target

Alle ube3a Antikörper anzeigen
ube3a (Ubiquitin Protein Ligase E3A (ube3a))

Reaktivität

  • 57
  • 12
  • 8
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 48
  • 9
Kaninchen

Klonalität

  • 46
  • 11
Polyklonal

Konjugat

  • 31
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ube3a Antikörper ist unkonjugiert

Applikation

  • 33
  • 16
  • 16
  • 13
  • 13
  • 13
  • 9
  • 9
  • 8
  • 5
  • 3
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Aufreinigung

    Immunogen affinity purified

    Reinheit

    ≥95 % as determined by SDS-PAGE

    Immunogen

    ubiquitin protein ligase E3A

    Isotyp

    IgG
  • Applikationshinweise

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

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

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    Haltbarkeit

    12 months
  • Target

    ube3a (Ubiquitin Protein Ligase E3A (ube3a))

    Andere Bezeichnung

    UBE3A

    Hintergrund

    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.

    Molekulargewicht

    110 kDa

    Gen-ID

    7337

    UniProt

    Q05086

    Pathways

    Intracellular Steroid Hormone Receptor Signaling Pathway
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