Cat: IPD-X41571

Recombinant Human DCLRE1A Protein ,His

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Analytical Data

  • Gene name

    DCLRE1A

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    (Beta-lactamase DCLRE1A)(SNM1 homolog A)(hSNM1)(hSNM1A)

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- His

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q6PJP8

  • Expression Region

    690-1040aa

  • Molecular Weight

    43.7 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

DCLRE1A, also known as DNA cross-link repair 1A, is a crucial protein involved in the process of DNA repair, particularly in the context of resolving DNA structures that arise from interstrand cross-links and double-strand breaks. It plays a significant role in maintaining genomic stability and preventing genetic diseases, including cancer. The study of DCLRE1A has gained attention due to its implication in various cellular processes, such as DNA damage response, replication stress, and apoptosis. Mutations or deficiencies in DCLRE1A have been linked to specific genetic disorders, which further underscores its importance in human health. The recombinant expression of DCLRE1A allows researchers to investigate its biochemical properties, interactions with other proteins, and its role in DNA repair pathways in a controlled laboratory setting. Understanding the functional mechanisms of DCLRE1A is critical for developing new therapeutic strategies for diseases associated with defective DNA repair mechanisms. Additionally, exploring the protein's structural characteristics through recombinant technology can provide insights into its enzymatic activity and regulatory functions, paving the way for potential interventions in cancer treatment and other genetic disorders. Overall, the study of recombinant DCLRE1A represents a vital area of research in molecular biology and genetics, with significant implications for therapeutic advancements and the comprehension of cellular responses to DNA damage.

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