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DLD antibody

DLD Reactivity: Human WB, IHC, IF, FACS Host: Mouse Monoclonal 4A10 unconjugated
Catalog No. ABIN2719488
  • Target See all DLD Antibodies
    DLD (Dihydrolipoamide Dehydrogenase (DLD))
    Reactivity
    • 46
    • 27
    • 26
    • 9
    • 5
    • 3
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 55
    • 6
    Mouse
    Clonality
    • 53
    • 8
    Monoclonal
    Conjugate
    • 38
    • 5
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DLD antibody is un-conjugated
    Application
    • 56
    • 24
    • 22
    • 12
    • 10
    • 10
    • 9
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS)
    Characteristics
    Homo sapiens dihydrolipoamide dehydrogenase (DLD)
    Purification
    Purified from mouse ascites fluids by affinity chromatography
    Immunogen
    Full length human recombinant protein of human DLD(NP_000099) produced in HEK293T cell.
    Clone
    4A10
    Isotype
    IgG1
    Top Product
    Discover our top product DLD Primary Antibody
  • Application Notes
    WB 1:2000, IHC 1:150, IF 1:100, FLOW 1:100,
    Comment

    The concentration of the product may vary between diferrent lots.

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5-1.0 mg/mL
    Buffer
    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
  • Target
    DLD (Dihydrolipoamide Dehydrogenase (DLD))
    Alternative Name
    DLD (DLD Products)
    Background
    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.
    Molecular Weight
    50.1 kDa
    Gene ID
    1738
    NCBI Accession
    NM_000108
    HGNC
    1738
    Pathways
    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
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