Cat: PA2000-890DB

Recombinant Human COX6c Protein,His

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Analytical Data

  • Gene name

    COX6c

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    COX6c;Cytochrome c oxidase subunit 6C

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P09669

  • Expression Region

    1-75aa

  • AA Sequence

    MAPEVLPKPRMRGLLARRLRNHMAVAFVLSLGVAALYKFRVADQRKKAYADFYRNYDVMKDFEEMRKAGIFQSVK

  • Molecular Weight

    8.7 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.

Quality inspection process

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Protein Description

COX6C, a subunit of cytochrome c oxidase (CCO) complex IV in the mitochondrial respiratory chain, plays a crucial role in cellular energy production through aerobic respiration. The study of COX6C has gained importance due to its implications in various metabolic disorders and mitochondrial diseases, which are often characterized by dysfunctional oxidative phosphorylation. Recent research has focused on the expression and functional characterization of COX6C, particularly in understanding its contribution to the assembly and stability of the CCO complex. In particular, the heterogeneity in COX6C expression across different tissues suggests a potential role in tissue-specific metabolic regulation. Furthermore, mutations or alterations in COX6C have been linked to pathological conditions, highlighting the need for detailed investigations into its structure and functionality. Recombination and production of COX6C as a recombinant protein allow for in-depth studies of its biochemical properties and interactions within the CCO complex, facilitating the exploration of its role in mitochondrial function. Understanding the mechanisms governing COX6C's activity and regulation could pave the way for targeted therapies in mitochondrial-related diseases, as well as provide insights into the fundamental processes of cellular respiration.

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