Cat: IPD-X39777

Recombinant Human CYP2C8 Protein ,His & Myc

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Analytical Data

  • Gene name

    CYP2C8

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    CYPIIC8 (Cytochrome P450 IIC2) (Cytochrome P450 MP-12) (Cytochrome P450 MP-20) (Cytochrome P450 form 1) (S-mephenytoin 4-hydroxylase)

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- His & C- Myc

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P10632

  • Expression Region

    27-490aa

  • Molecular Weight

    60.1 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

CYP2C8, a member of the cytochrome P450 family, plays a crucial role in drug metabolism and is primarily involved in the oxidation of various xenobiotics and endogenous compounds. Understanding CYP2C8 function is essential for predicting drug interactions, metabolite formation, and individual variability in drug responses. Genetic polymorphisms and environmental factors can significantly affect CYP2C8 activity, leading to altered pharmacokinetics and increased risk of adverse drug reactions. Research has focused on the recombinant expression of CYP2C8 to facilitate detailed studies of its enzymatic properties, substrate specificity, and interaction with inhibitors or inducers. Advances in recombinant protein technology have enabled the production of CYP2C8 in heterologous systems, providing insights into its structural and functional aspects. Furthermore, studies on CYP2C8 have implications in personalized medicine, as understanding its variability can aid in optimizing drug dosing and minimizing toxicity for patients with different genetic backgrounds. Overall, the investigation of CYP2C8 recombinant protein is vital for enhancing the understanding of metabolic pathways and improving the safety and efficacy of therapeutic interventions.

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