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GLUD1 Antikörper

Dieser Kaninchen Monoklonal Antikörper erkennt spezifisch GLUD1 in WB, IHC und IF. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7267411

Kurzübersicht für GLUD1 Antikörper (ABIN7267411)

Target

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

Reaktivität

  • 40
  • 26
  • 24
  • 14
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 49
  • 3
  • 1
Kaninchen

Klonalität

  • 40
  • 13
Monoklonal

Konjugat

  • 28
  • 6
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser GLUD1 Antikörper ist unkonjugiert

Applikation

  • 39
  • 27
  • 19
  • 18
  • 15
  • 13
  • 11
  • 5
  • 4
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Verwendungszweck

    GLUD1 Rabbit mAb

    Kreuzreaktivität

    Human, Maus, Ratte

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human GLUD1

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,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.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    GLUD1 (Glutamate Dehydrogenase 1 (GLUD1))

    Andere Bezeichnung

    GLUD1

    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. [provided by RefSeq, Jan 2016],GDH, GDH1, GLUD,Amino acid metabolism,Cancer,Cell Biology & Developmental Biology,Endocrine & Metabolism,Signal Transduction,GLUD1

    Molekulargewicht

    50kDa

    Gen-ID

    2746

    UniProt

    P00367

    Pathways

    Positive Regulation of Peptide Hormone Secretion, Warburg Effekt
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