Cat: IPD-X41409

Recombinant Human NF1 Protein ,His & Myc

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Analytical Data

  • Gene name

    NF1

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    (Neurofibromatosis-related protein NF-1)

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- His & C- Myc

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P21359

  • Expression Region

    1566-1837aa

  • Molecular Weight

    38.7 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

Neurofibromatosis type 1 (NF1) is a genetic disorder caused by mutations in the NF1 gene, which encodes the neurofibromin protein, a key regulator of the RAS signaling pathway. Neurofibromin functions as a tumor suppressor, as it negatively regulates RAS activity, thus playing a crucial role in cell growth and differentiation. Patients with NF1 commonly present with benign tumors known as neurofibromas, as well as an increased risk of malignant tumors and various neurological issues. The study of NF1 recombinant protein is critical for understanding the molecular mechanisms underlying NF1 and the biological functions of neurofibromin. By expressing and purifying NF1 recombinant protein, researchers aim to investigate its structure, function, and interactions with other cellular proteins, which can provide insights into the development of targeted therapies. This research not only enhances our understanding of NF1 pathophysiology but also aids in the identification of potential biomarkers for early diagnosis and prognosis. Furthermore, the characterization of NF1 recombinant protein may facilitate drug discovery efforts, leading to innovative treatments that specifically address the complications associated with NF1, ultimately improving patient outcomes and quality of life.

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