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DLD Antikörper

DLD Reaktivität: Human WB, IHC, IF, FACS Wirt: Maus Monoclonal 4E11 unconjugated
Produktnummer ABIN2719485
  • Target Alle DLD Antikörper anzeigen
    DLD (Dihydrolipoamide Dehydrogenase (DLD))
    Reaktivität
    • 46
    • 27
    • 26
    • 9
    • 5
    • 3
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 55
    • 6
    Maus
    Klonalität
    • 53
    • 8
    Monoklonal
    Konjugat
    • 38
    • 5
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser DLD Antikörper ist unkonjugiert
    Applikation
    • 56
    • 24
    • 22
    • 12
    • 10
    • 10
    • 9
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS)
    Produktmerkmale
    Homo sapiens dihydrolipoamide dehydrogenase (DLD)
    Aufreinigung
    Purified from mouse ascites fluids by affinity chromatography
    Immunogen
    Full length human recombinant peotein of human DLD(NP_000099) produced in HEK293T cell.
    Klon
    4E11
    Isotyp
    IgG1
    Top Product
    Discover our top product DLD Primärantikörper
  • Applikationshinweise
    WB 1:2000, IHC 1:150, IF 1:100, FLOW 1:100,
    Kommentare

    The concentration of the product may vary between diferrent lots.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    0.5-1.0 mg/mL
    Buffer
    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
    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
  • Target
    DLD (Dihydrolipoamide Dehydrogenase (DLD))
    Andere Bezeichnung
    DLD (DLD Produkte)
    Hintergrund
    This gene encodes the L protein of the mitochondrial glycine cleavage system. The L protein, also named dihydrolipoamide dehydrogenase, is also a component of the pyruvate dehydrogenase complex, the alpha-ketoglutarate dehydrogenase complex, and the branched-chain alpha-keto acide dehydrogenase complex. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency.
    Molekulargewicht
    50.1 kDa
    Gen-ID
    1738
    NCBI Accession
    NM_000108
    HGNC
    1738
    Pathways
    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
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