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Peroxisomal Bifunctional Enzyme Antikörper (Middle Region)

Der Kaninchen Polyklonal Anti-Peroxisomal Bifunctional Enzyme-Antikörper wurde für WB validiert. Er ist geeignet, Peroxisomal Bifunctional Enzyme in Proben von Human zu detektieren.
Produktnummer ABIN5514454

Kurzübersicht für Peroxisomal Bifunctional Enzyme Antikörper (Middle Region) (ABIN5514454)

Target

Peroxisomal Bifunctional Enzyme (ECHP)

Reaktivität

Human

Wirt

Kaninchen

Klonalität

Polyklonal

Applikation

Western Blotting (WB)
  • Bindungsspezifität

    Middle Region

    Sequenz

    VIAVDSDKNQ LATANKMITS VLEKEASKMQ QSGHPWSGPK PRLTSSVKEL

    Produktmerkmale

    This is a rabbit polyclonal antibody against ECHP. It was validated on Western Blot.

    Aufreinigung

    Affinity purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the middle region of Human ECHP
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target

    Peroxisomal Bifunctional Enzyme (ECHP)

    Andere Bezeichnung

    ECHP

    Hintergrund

    The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene.

    Alias Symbols: EHHADH, ECHD,

    Protein Size: 723

    Gen-ID

    1962

    NCBI Accession

    NP_001957

    UniProt

    Q08426
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