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GLUD1 / GLUD2 (AA 54-553) Antikörper

Der Kaninchen Polyklonal anti-GLUD1 / GLUD2 Antikörper (ABIN7875655) detektiert spezifisch GLUD1 / GLUD2 in ELISA, WB, IF, FACS und IHC (p). Dieser Antikörper reagiert spezifisch mit Proben aus Human, Maus und Ratte.
Produktnummer ABIN7875655
644,88 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für GLUD1 / GLUD2 (AA 54-553) Antikörper (ABIN7875655)

Target

GLUD1 / GLUD2

Reaktivität

Human, Maus, Ratte

Wirt

  • 1
  • 1
Kaninchen

Klonalität

  • 2
Polyklonal

Konjugat

  • 2
Unkonjugiert

Applikation

  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
ELISA, Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Bindungsspezifität

    • 1
    • 1
    AA 54-553

    Verwendungszweck

    GLUD1/2 Antibody / GDH1/2

    Aufreinigung

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids S54-A553) was used as the immunogen for the GLUD1/2 antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the GLUD1/2 antibody should be determined by the researcher.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    After reconstitution, the GLUD1/2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    GLUD1 / GLUD2

    Andere Bezeichnung

    GLUD1/2

    Hintergrund

    This gene encodes Glutamate dehydrogenase, which is a mitochondrial matrix enzyme that catalyzes the oxidative deamination of glutamate to alpha-ketoglutarate and ammonia. This enzyme has an important role in regulating amino acid-induced insulin secretion. It is allosterically activated by ADP and inhibited by GTP and ATP. Activating mutations in this gene are a common cause of congenital hyperinsulinism. Alternative splicing of this gene results in multiple transcript variants. The related glutamate dehydrogenase 2 gene on the human X-chromosome originated from this gene via retrotransposition and encodes a soluble form of glutamate dehydrogenase. Related pseudogenes have been identified on chromosomes 10, 18 and X.

    UniProt

    P00367
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