Cat: PA1000-5691

Recombinant Human NPC1 Protein,His

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Analytical Data

  • Gene name

    NPC1

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    NPC1;NPC intracellular cholesterol transporter 1

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    O15118

  • Expression Region

    151-250aa

  • AA Sequence

    GFANAMYNACRDVEAPSSNDKALGLLCGKDADACNATNWIEYMFNKDNGQ APFTITPVFSDFPVHGMEPMNNATKGCDESVDEVTAPCSCQDCSIVCGPK

  • 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.

Quality inspection process

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Protein Description

Niemann-Pick C1-like 1 protein (NPC1) is a crucial membrane protein primarily known for its role in cholesterol and lipid transport within the endosomal-lysosomal pathway. Mutations in the NPC1 gene are linked to Niemann-Pick disease type C, a severe neurodegenerative disorder characterized by cholesterol accumulation in various tissues, particularly the brain. Research into NPC1 has gained momentum due to its significant implications in cellular lipid homeostasis, disease progression, and potential therapeutic avenues. The recombinant expression of NPC1 protein allows for detailed structural and functional studies, which are essential for understanding its mechanisms and interactions at a molecular level. Additionally, NPC1 has garnered attention in the context of viral infections, including its involvement in the entry of several pathogens, making it a potential target for antiviral strategies. By generating and characterizing NPC1 recombinant proteins, researchers aim to elucidate its role in lipid metabolism, develop effective treatment options for Niemann-Pick disease, and investigate its relevance in infectious disease contexts, thereby contributing to a broader understanding of lipid biology and disease mechanisms.

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