Cat: IPD-X39376

Recombinant Human NDUFS1 Protein,His

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Analytical Data

  • Gene name

    NDUFS1

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    CI-75Kd; NADH-Coenzyme Q Reductase; NADH Dehydrogenase Iron-Sulfur Protein 1; NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial

  • Species

    Human

  • Source

    E. coli

  • Tag

    N-His

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P28331

  • Expression Region

    Ala524~Cys727

  • Molecular Weight

    26kDa

  • Endotoxin

    < 1.0 EU per μg protein as determined by the LAL method.

  • Form

    Freeze-dried powder

  • Buffer formulation

    PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.

  • Reconstitution

    Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.

  • Customization

    Site-directed mutagenesis Custom tag design Custom buffer formulation Custom full-length protein production

  • Stability Test

    The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.

  • Storage & Shelf Life

    Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.

  • Shipping

    In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.

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Protein Description

NDUFS1 is a critical subunit of the mitochondrial respiratory chain complex I, also known as NADH:ubiquinone oxidoreductase, which plays a vital role in cellular energy production through oxidative phosphorylation. Deficiencies or mutations in the NDUFS1 gene have been implicated in a range of mitochondrial disorders, resulting in severe clinical phenotypes, including neurodegenerative diseases and myopathies. Understanding the function and structure of NDUFS1 is essential for elucidating its role in mitochondrial bioenergetics and for developing potential therapeutic strategies to address associated pathologies. Recent advances in recombinant protein technology have enabled the expression and purification of NDUFS1, facilitating in-depth studies of its enzymatic activity, interaction with other mitochondrial components, and its impact on overall cellular metabolism. These studies not only contribute to our understanding of mitochondrial dysfunction but also pave the way for innovative treatments targeting the underlying causes of mitochondrial diseases. As a result, recombinant NDUFS1 protein research is crucial for both basic science and translational medicine, highlighting its significance in the field of bioenergetics and genetic disorders.

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