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DLD antibody

The Rabbit Polyclonal anti-DLD antibody has been validated for WB, IF, ICC and IHC (p). It is suitable to detect DLD in samples from Human. There is 1 publication available.
Catalog No. ABIN2854985

Quick Overview for DLD antibody (ABIN2854985)

Target

See all DLD Antibodies
DLD (Dihydrolipoamide Dehydrogenase (DLD))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This DLD antibody is un-conjugated

Application

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Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Grade

KO Validated
  • Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Rabbit Polyclonal antibody to DLD (dihydrolipoamide dehydrogenase)
    DLD antibody

    Purification

    Affinity purified by Protein A.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human DLD. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: Mouse brain , 293T , PC-12 , Rat2 , HeLa

    Validation: KO/KD

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1XPBS ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Shin, Lee, You, Kim, Roh: "Dihydrolipoamide dehydrogenase regulates cystine deprivation-induced ferroptosis in head and neck cancer." in: Redox biology, Vol. 30, pp. 101418, (2020) (PubMed).

  • Target

    DLD (Dihydrolipoamide Dehydrogenase (DLD))

    Alternative Name

    dihydrolipoamide dehydrogenase

    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.

    Cellular Localization: Mitochondrion matrix

    Molecular Weight

    54 kDa

    Gene ID

    1738

    UniProt

    P09622

    Pathways

    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
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