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DLD Antikörper

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch DLD in WB, IHC, ELISA und IF. Er zeigt eine Reaktivität gegenüber Human und Maus.
Produktnummer ABIN7113484

Kurzübersicht für DLD Antikörper (ABIN7113484)

Target

Alle DLD Antikörper anzeigen
DLD (Dihydrolipoamide Dehydrogenase (DLD))

Reaktivität

  • 46
  • 27
  • 27
  • 7
  • 5
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Human, Maus

Wirt

  • 53
  • 6
Kaninchen

Klonalität

  • 49
  • 10
Polyklonal

Konjugat

  • 37
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser DLD Antikörper ist unkonjugiert

Applikation

  • 54
  • 23
  • 22
  • 13
  • 13
  • 10
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)
  • Aufreinigung

    Immunogen affinity purified

    Reinheit

    ≥95 % as determined by SDS-PAGE

    Immunogen

    dihydrolipoamide dehydrogenase

    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 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.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Haltbarkeit

    12 months
  • Target

    DLD (Dihydrolipoamide Dehydrogenase (DLD))

    Andere Bezeichnung

    DLD

    Hintergrund

    Synonyms:GCSL, LAD, PHE3 Background:This gene encodes a member of the class-I pyridine nucleotide-disulfide oxidoreductase family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In homodimeric form, the encoded protein functions as a dehydrogenase and is found in several multi-enzyme complexes that regulate energy metabolism. However, as a monomer, this protein can function as a protease. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency. Alternative splicing results in multiple transcript variants.

    Molekulargewicht

    54 kDa

    Gen-ID

    1738

    UniProt

    P09622

    Pathways

    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
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