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DLD Antikörper

Dieses Kaninchen Monoklonal-Antikörper erkennt spezifisch DLD in WB, IHC und IF. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7266766

Kurzübersicht für DLD Antikörper (ABIN7266766)

Target

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

Reaktivität

  • 50
  • 30
  • 29
  • 7
  • 5
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 58
  • 7
Kaninchen

Klonalität

  • 55
  • 10
Monoklonal

Konjugat

  • 43
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser DLD Antikörper ist unkonjugiert

Applikation

  • 60
  • 28
  • 23
  • 18
  • 15
  • 13
  • 7
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Verwendungszweck

    DLDH/DLD Rabbit mAb

    Kreuzreaktivität

    Human, Maus, Ratte

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human DLDH/DLD

    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

    DLD (Dihydrolipoamide Dehydrogenase (DLD))

    Andere Bezeichnung

    DLD

    Hintergrund

    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. [provided by RefSeq, Jan 2014],DLDD, DLDH, E3, GCSL, LAD, PHE3,Amino acid metabolism,Cancer,Carbohydrate metabolism,Endocrine & Metabolism,Signal Transduction,DLD

    Molekulargewicht

    56kDa

    Gen-ID

    1738

    UniProt

    P09622

    Pathways

    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
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