Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

Ubiquitin Protein Ligase E3A (ube3a) (N-Term) Peptid

ube3a Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN985847
150,78 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 15 bis 21 Werktagen

Kurzübersicht für Ubiquitin Protein Ligase E3A (ube3a) (N-Term) Peptid (ABIN985847)

Target

ube3a (Ubiquitin Protein Ligase E3A (ube3a))

Spezies

Human

Quelle

  • 2
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    N-Term

    Produktmerkmale

    This is a synthetic peptide designed for use in combination with anti-UBE3A antibody (Catalog #: ARP42950_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Aufreinigung

    Purified
  • Applikationshinweise

    Each Investigator should determine their own optimal working dilution for specific applications.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Konzentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handhabung

    Avoid repeated freeze-thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

    ube3a (Ubiquitin Protein Ligase E3A (ube3a))

    Hintergrund

    UBE3A is 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.Western blots using two different antibodies against two unique regions of this protein target confirm the same apparent molecular weight in our tests.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.

    Alias Symbols: ANCR, AS, E6-AP, EPVE6AP, FLJ26981, HPVE6A

    Protein Interaction Partner: UBE2L3,UBE2L6,AR,BLK,BPY2B,BPY2C,BPY2C,EAPP,MCM7,PGR,PHF17,RARA,SCAMP1,SHBG,SMAD9,TP53,UBE2D1,UBE2D3,UBE2E1,UBE2G1,UBE2G2,UBE2L3,UBE2L6,UBE3A,UBQLN2,BARD1,BLK,BPY2,BRCA1,ESR2,LCK,MCM7,PGR,TSC2,UBE2D1,UBE2D2,UBE2D3,UBE2L3,UBQLN1,UBQLN2

    Protein Size: 875

    Molekulargewicht

    101 kDa

    Gen-ID

    7337

    NCBI Accession

    NM_000462, NP_000453

    UniProt

    Q05086
Sie sind hier:
Chat with us!