OGDH Antibody [F21L21]

Catalog No.: F9941

    Application: Reactivity:
    • Lane 1: LNCap, Lane 2: Hela, Lane 3: DLD-1, Lane 4: MCF7
    1/

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    代表番号: 045-509-1970|電子メール:sales@selleck.co.jp

    使用情報

    Dilution
    1:1000
    1:50
    Application
    WB, IP
    Source
    Rabbit Monoclonal Antibody
    Reactivity
    Human, Mouse, Rat, Monkey
    Storage Buffer
    PBS, pH 7.2+50% Glycerol+0.05% BSA+0.01% NaN3
    Storage (from the date of receipt)
    -20°C (avoid freeze-thaw cycles), 2 years
    Predicted MW
    110 kDa

    Datasheet & SDS

    生物学的記述

    Specificity
    OGDH Antibody [F21L21] detects endogenous levels of total OGDH protein.
    Clone
    F21L21
    Synonym(s)
    2-oxoglutarate dehydrogenase, mitochondrial; Alpha-ketoglutarate dehydrogenase; OGDH
    Background
    OGDH serves as the E1 subunit of the 2-oxoglutarate dehydrogenase multienzyme complex within the tricarboxylic acid cycle in eukaryotic mitochondria. The complex assembles with dihydrolipoamide S-succinyltransferase and dihydrolipoamide dehydrogenase to decarboxylate 2-oxoglutarate into succinyl-CoA alongside CO2 release and NADH generation. Calcium ions bind to specific sites on OGDH, including regions like D114ADLD and E139SDLD equivalents, lowering the Km for 2-oxoglutarate to enhance substrate affinity under physiological concentrations. ADP activates the complex by decreasing substrate Km, while ATP and NADH exert inhibitory effects by elevating Km values and shifting NADH sensitivity thresholds. These allosteric modulations integrate OGDH activity with cellular energy status, adenine nucleotide ratios, and redox balance, channeling TCA flux toward oxidative phosphorylation or biosynthetic demands. The protein assembles into a cubic arrangement with cofactor-binding domains that swing relative to the core during catalysis, facilitating thiamine pyrophosphate-dependent decarboxylation, lipoamide swinging for acyl transfer, and NADH production. OGDH sustains NADH supply for electron transport while modulating reactive oxygen species from associated flavins. Dysregulation through mutations or inhibition impairs complex assembly and flux, linking to encephalopathy and neurodegenerative decline via mitochondrial dysfunction.
    References

    技術サポート

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