Cat: IPD-X24763

Recombinant Human Amyloid Precursor/APP-695 Protein (HEK293),hFc

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Analytical Data

  • Gene name

    Amyloid Precursor/APP-695

  • 简介

    Amyloid Precursor/APP-695 Protein, Human (HEK293, Fc) is an Amyloid Precursor (APP) protein with C-Fc. Amyloid Precursor Protein can be used for the study of brain development, learning and memory, synaptic plasticity, and neurodegeneration[1].

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    rHuAmyloid Precursor, C-Fc; Amyloid-Precursor

  • Species

    Human

  • Source

    HEK293

  • Tag

    C-hFc

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P05067-4

  • Expression Region

    L18-K612

  • AA Sequence

    LEVPTDGNAGLLAEPQIAMFCGRLNMHMNVQNGKWDSDPSGTKTCIDTKEGILQYCQEVYPELQITNVVEANQPVTIQNWCKRGRKQCKTHPHFVIPYRCLVGEFVSDALLVPDKCKFLHQERMDVCETHLHWHTVAKETCSEKSTNLHDYGMLLPCGIDKFRGVEFVCCPLAEESDNVDSADAEEDDSDVWWGGADTDYADGSEDKVVEVAEEEEVAEVEEEEADDDEDDEDGDEVEEEAEEPYEEATERTTSIATTTTTTTESVEEVVRVPTTAASTPDAVDKYLETPGDENEHAHFQKAKERLEAKHRERMSQVMREWEEAERQAKNLPKADKKAVIQHFQEKVESLEQEAANERQQLVETHMARVEAMLNDRRRLALENYITALQAVPPRPRHVFNMLKKYVRAEQKDRQHTLKHFEHVRMVDPKKAAQIRSQVMTHLRVIYERMNQSLSLLYNVPAVAEEIQDEVDELLQKEQNYSDDVLANMISEPRISYGNDALMPSLTETKTTVELLPVNGEFSLDDLQPWHSFGADSVPANTENEVEPVDARPAADRGLTTRPGSGLTNIKTEEISEVKMDAEFRHDSGYEVHHQK

  • Protein Length

    Partial

  • Molecular Weight

    120-145 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

Related Products

Protein Description

Amyloid Precursor Protein (APP) is a transmembrane protein crucially involved in the pathogenesis of Alzheimer’s disease (AD). The APP gene, located on chromosome 21, is known to undergo proteolytic processing by enzymes such as β-secretase and γ-secretase, resulting in the production of amyloid-beta (Aβ) peptides. These peptides can aggregate and form plaques, which are hallmark features of AD pathology. Research has increasingly focused on elucidating the structure and function of APP-695, the predominant isoform of APP in neurons, as it plays a significant role in neuronal development and synaptic function. Recombinant APP-695 protein has become an important tool for scientists, enabling the study of APP processing, Aβ generation, and the modulation of these pathways by potential therapeutic agents. Understanding the detailed mechanisms of APP-695 can provide insights into the molecular underpinnings of AD and aid in the development of targeted treatments that could modify the disease’s course or prevent its onset. This research is particularly relevant given the aging population and the increasing incidence of neurodegenerative diseases, making the investigation of APP-695 and its associated pathways vital for advancing our understanding and management of Alzheimer's disease.

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