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GLUD1 / GLUD2 (AA 54-553) Antikörper (HRP)

Der Kaninchen Polyklonal anti-GLUD1 / GLUD2 Antikörper wird verwendet zum Nachweis von GLUD1 / GLUD2 in Proben von Human, Maus und Ratte. Er wurde validiert für ELISA, WB und IHC.
Produktnummer ABIN7993582
720,50 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 8 bis 12 Werktagen

Kurzübersicht für GLUD1 / GLUD2 (AA 54-553) Antikörper (HRP) (ABIN7993582)

Target

GLUD1 / GLUD2

Reaktivität

Human, Maus, Ratte

Wirt

  • 12
  • 1
Kaninchen

Klonalität

  • 13
Polyklonal

Konjugat

  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
HRP

Applikation

  • 11
  • 5
  • 5
  • 4
  • 4
  • 2
  • 1
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
  • Bindungsspezifität

    • 12
    • 1
    AA 54-553

    Verwendungszweck

    Anti-GLUD1/2 Antibody HRP Conjugated

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Aufreinigung

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human GLUD1/2 recombinant protein (Position: S54-A553).

    Isotyp

    IgG
  • Applikationshinweise

    Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

    Haltbarkeit

    12 months
  • Target

    GLUD1 / GLUD2

    Andere Bezeichnung

    GLUD1/2

    Hintergrund

    Background: 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.

    Gene Full Name: glutamate dehydrogenase 1/2

    Gen-ID

    2746, 2747

    UniProt

    P00367
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