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DLD Antikörper

DLD Reaktivität: Human, Maus, Ratte, Hund, Affe WB, FACS Wirt: Maus Monoclonal 8A10 unconjugated
Produktnummer ABIN2719484
  • Target Alle DLD Antikörper anzeigen
    DLD (Dihydrolipoamide Dehydrogenase (DLD))
    Reaktivität
    • 46
    • 27
    • 26
    • 9
    • 5
    • 3
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte, Hund, Affe
    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), Flow Cytometry (FACS)
    Produktmerkmale
    Homo sapiens dihydrolipoamide dehydrogenase (DLD)
    Aufreinigung
    Purified from mouse ascites fluids by affinity chromatography
    Immunogen
    Full length human recombinant protein of human DLD(NP_000099) produced in HEK293T cell.
    Klon
    8A10
    Isotyp
    IgG1
    Top Product
    Discover our top product DLD Primärantikörper
  • Applikationshinweise
    WB 1:500, 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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