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Peroxisomal Bifunctional Enzyme Antikörper (Middle Region)

Der Kaninchen Polyklonal anti-Peroxisomal Bifunctional Enzyme Antikörper wird verwendet zum Nachweis von Peroxisomal Bifunctional Enzyme in Proben von Human. Er wurde validiert für WB.
Produktnummer ABIN5514454
534,11 €
Zzgl. Versandkosten 20,00 € und MwSt
Lieferung nach: Deutschland
Lieferung in 6 bis 8 Werktagen

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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