Cat: IPD-X41572

Recombinant Mouse Cyp3a11 Protein ,His & Myc

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Analytical Data

  • Gene name

    Cyp3a11

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    (CYPIIIA11)(Cytochrome P-450IIIAM1)(Cytochrome P-450UT)

  • Species

    Mouse

  • Source

    E. coli

  • Tag

    N- His & C- Myc

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q64459

  • Expression Region

    1-504aa

  • Molecular Weight

    65.3 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

CYP3A11 is a member of the cytochrome P450 superfamily of enzymes, primarily involved in the metabolism of various endogenous and exogenous compounds, including drugs and steroids. Its role in pharmacokinetics and toxicology has garnered significant attention, particularly due to its potential impact on drug efficacy and safety. Variations in CYP3A11 expression and activity can lead to interindividual differences in drug metabolism, making it a critical target for personalized medicine approaches. Understanding the functional characteristics of CYP3A11 requires the production of recombinant protein, allowing researchers to study its enzymatic activity in vitro. Additionally, the recombinant CYP3A11 protein serves as a valuable tool for exploring drug-drug interactions, as well as for screening potential drug candidates. With the increasing focus on precision pharmacotherapy, characterizing the biochemical properties and mechanisms of CYP3A11 will pave the way for optimizing therapeutic strategies and minimizing adverse drug reactions in diverse patient populations. As such, research into the recombinant expression and functional analysis of CYP3A11 is crucial for advancing our knowledge of metabolic pathways and enhancing the safety and effectiveness of pharmacological treatments.

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