Cat: PA1000-8825

Recombinant Human PSEN1 Protein,His

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Analytical Data

  • Gene name

    PSEN1

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    PSEN1;Presenilin

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P49768

  • Expression Region

    280-379aa

  • AA Sequence

    PALIYSSTMVWLVNMAEGDPEAQRRVSKNSKYNAESTERESQDTVAENDD GGFSEEWEAQRDSHLGPHRSTPESRAAVQELSSSILAGEDPEERGVKLGL

  • Molecular Weight

    37 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.

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Protein Description

PSEN1, or Presenilin-1, is a crucial protein implicated in the pathogenesis of familial Alzheimer's disease (FAD). It forms a part of the gamma-secretase complex, an enzyme responsible for the cleavage of amyloid precursor protein (APP), leading to the production of beta-amyloid peptides. Mutations in the PSEN1 gene are associated with early-onset Alzheimer's, making it a key target for research into disease mechanisms and potential therapeutic strategies. Studies have revealed that PSEN1 mutations can alter gamma-secretase activity, impacting amyloid beta generation and contributing to neurodegeneration. Understanding the structure and function of PSEN1 is essential for developing targeted treatments. Recent advancements in recombinant protein technologies have enabled the production of PSEN1 in various systems, allowing researchers to analyze its biochemical properties, interactions with other cellular components, and role in cellular signaling pathways. By obtaining PSEN1 as a recombinant protein, scientists can conduct detailed studies on the molecular basis of Alzheimer's disease, explore the effects of specific mutations, and assess the efficacy of potential drug candidates aimed at modulating gamma-secretase activity. As research continues to unfold, PSEN1 remains a focal point in unraveling the complexities of Alzheimer’s disease and developing innovative approaches for intervention.

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