Cat: IPD-X40752

Recombinant Human POLG2 Protein ,His & SUMO

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Analytical Data

  • Gene name

    POLG2

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    DNA polymerase gamma accessory 55KDA subunit ;p55Mitochondrial DNA polymerase accessory subunitMtPolBPolG-beta

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- His-SUMO

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q9UHN1

  • Expression Region

    1-485aa

  • Molecular Weight

    70.9 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

POLG2, or polymerase gamma subunit 2, is a crucial component of the mitochondrial DNA polymerase complex, which plays a significant role in mitochondrial DNA replication and repair. The study of POLG2 is essential due to its involvement in various mitochondrial disorders, which can lead to conditions such as neurodegeneration, myopathy, and premature aging. Mutations in the POLG2 gene are associated with several human diseases, indicating its importance in maintaining mitochondrial function and cellular health. Research focused on recombinant POLG2 proteins aims to better understand the enzyme’s structure-function relationship and its interaction with other components of the mitochondrial DNA replication machinery. By producing and characterizing recombinant POLG2, scientists can explore its catalytic mechanisms, substrate specificity, and the effects of disease-linked mutations. This research not only elucidates the role of POLG2 in mitochondrial biology but also opens avenues for potential therapeutic interventions targeting mitochondrial dysfunction, highlighting the protein's significance in both basic and applied biomedical research. Understanding POLG2's function and regulation may pave the way for novel strategies to address mitochondrial diseases and enhance mitochondrial health, thus contributing to the broader field of mitochondrial medicine.

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