Cat: PA2000-3593

Recombinant Human UQCR11 Protein,His

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Analytical Data

  • Gene name

    UQCR11

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    UQCR11;UQCR;Cytochrome b-c1 complex subunit 10

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    O14957

  • Expression Region

    1-56aa

  • AA Sequence

    MVTRFLGPRYRELVKNWVPTAYTWGAVGAVGLVWATDWRLILDWVPYINGKFKKDN

  • Molecular Weight

    33.6 kDa

  • 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

UQCR11, also known as ubiquinone-cytochrome c reductase assembly factor, plays a crucial role in the assembly and function of the mitochondrial respiratory chain complex III. Research on UQCR11 has garnered interest due to its potential implications in mitochondrial disorders and other metabolic diseases. Mitochondria are essential for energy production in cells, and any dysfunction in the respiratory chain can lead to severe cellular consequences, including reduced ATP synthesis and increased oxidative stress. Studies indicate that mutations or deficiencies in UQCR11 can disrupt the assembly of the respiratory chain complexes, leading to compromised mitochondrial function and various pathological conditions. Additionally, UQCR11 has been implicated in certain types of cancer, where altered mitochondrial activity can contribute to the malignancy's development and progression. The characterization of UQCR11’s structure and function not only enhances the understanding of mitochondrial biology but also offers potential therapeutic avenues for conditions related to mitochondria, underlining the importance of this protein in both basic and clinical research.

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