Cat: IPD-X25346

Recombinant Human p53 Protein,His

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Analytical Data

  • Gene name

    p53

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    TP53; LFS1; TRP53; Li-Fraumeni Syndrome; Cellular tumor antigen p53; Antigen NY-CO-13; Phosphoprotein p53; Tumor suppressor p53

  • Species

    Human

  • Source

    E. coli

  • Tag

    N-His

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P04637

  • Expression Region

    Gly108~Lys370

  • Molecular Weight

    34kDa

  • 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

The p53 protein, often referred to as the "guardian of the genome," plays a crucial role in regulating the cell cycle and maintaining genomic stability. It is encoded by the TP53 gene and acts as a tumor suppressor, preventing the proliferation of cells with damaged DNA. Mutations in the TP53 gene are found in approximately half of all human cancers, underscoring its significance in cancer biology. Research into p53 has gained momentum due to its pivotal role in regulating apoptosis, DNA repair, and cellular senescence. Recombinant p53 protein has been developed for various applications, including studying its functional mechanisms, developing cancer therapies, and designing targeted treatments that restore the activity of mutated forms of p53. Furthermore, innovative techniques such as CRISPR/Cas9 genome editing are being explored to create cellular models that express mutated p53, enhancing our understanding of its role in tumorigenesis. The characterization and application of recombinant p53 allow researchers to elucidate its biochemical pathways and interactions with other cellular proteins, offering insights into potential therapeutic strategies to combat cancers associated with p53 dysfunction. Overall, p53 and its recombinant protein derivatives represent a vital area of research in oncology, with the potential to transform cancer treatment paradigms and improve patient outcomes.

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