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GLUD1 Antikörper

Der Kaninchen Polyklonal Anti-GLUD1-Antikörper wurde für WB, IHC, IP und ELISA validiert. Er ist geeignet, GLUD1 in Proben von Human, Maus und Ratte zu detektieren.
Produktnummer ABIN5697821

Kurzübersicht für GLUD1 Antikörper (ABIN5697821)

Target

Alle GLUD1 Antikörper anzeigen
GLUD1 (Glutamate Dehydrogenase 1 (GLUD1))

Reaktivität

  • 35
  • 19
  • 17
  • 17
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 47
  • 6
  • 1
Kaninchen

Klonalität

  • 46
  • 8
Polyklonal

Konjugat

  • 38
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser GLUD1 Antikörper ist unkonjugiert

Applikation

  • 40
  • 27
  • 18
  • 15
  • 15
  • 11
  • 6
  • 5
  • 5
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunoprecipitation (IP), ELISA
  • Immunogen

    glutamate dehydrogenase 1

    Isotyp

    IgG
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Kommentare

    HeLa cells were subjected to SDS PAGE followed by western blot with FNab03498(GLUD1 antibody) at dilution of 1:3000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol  pH 7.3

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handhabung

    Avoid repeated freeze / thaw cycles.

    Lagerung

    -20 °C

    Haltbarkeit

    12 months
  • Target

    GLUD1 (Glutamate Dehydrogenase 1 (GLUD1))

    Andere Bezeichnung

    GLUD1

    Hintergrund

    Synonyms:GLUD 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.

    Molekulargewicht

    45-55 kDa

    Gen-ID

    2746

    UniProt

    P00367

    Pathways

    Positive Regulation of Peptide Hormone Secretion, Warburg Effekt
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