Cat: IPD-X22919

Recombinant Human PROS1 Protein (HEK293),His

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Analytical Data

  • Gene name

    PROS1

  • 简介

    Protein S/PROS1 Proteinas are potent antagonists of BMP4 and inhibit BMP4 by binding to BMP4 and preventing receptor interaction. This change redirects neural stem cells from gliogenesis to neurogenesis, thereby promoting the differentiation of neurons in the brain. Protein S/PROS1 Protein, Human (HEK293, His) is the recombinant human-derived protein S/PROS1 protein, expressed by HEK293 , with C-His labeled tag.

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Biological Activity

    Measured by its binding ability in a functional ELISA.When Recombinant Human Tyro3/Dtk (HY-P78657) is immobilized at 1 μg/mL, 100 μL/well, Recombinant Human Protein S/PROS1 binds with an ED50 of 0.04361 μg/mL. Measured by its binding ability in a functional ELISA.When Recombinant Human Tyro3/Dtk (HY-P78657) is immobilized at 1 μg/mL, 100 μL/well, Recombinant Human Protein S/PROS1 binds with an ED50 of 0.04361 μg/mL.

  • Alternative Names

    Vitamin K-dependent protein S; PROS1; PROS

  • Species

    Human

  • Source

    HEK293

  • Tag

    C-10*His

  • Purity

    Greater than 95% as determined by SDS-PAGE.

  • Uniprot

    P07225

  • Expression Region

    N25-S676

  • AA Sequence

    NFLSKQQASQVLVRKRRANSLLEETKQGNLERECIEELCNKEEAREVFENDPETDYFYPKYLVCLRSFQTGLFTAARQSTNAYPDLRSCVNAIPDQCSPLPCNEDGYMSCKDGKASFTCTCKPGWQGEKCEFDINECKDPSNINGGCSQICDNTPGSYHCSCKNGFVMLSNKKDCKDVDECSLKPSICGTAVCKNIPGDFECECPEGYRYNLKSKSCEDIDECSENMCAQLCVNYPGGYTCYCDGKKGFKLAQDQKSCEVVSVCLPLNLDTKYELLYLAEQFAGVVLYLKFRLPEISRFSAEFDFRTYDSEGVILYAESIDHSAWLLIALRGGKIEVQLKNEHTSKITTGGDVINNGLWNMVSVEELEHSISIKIAKEAVMDINKPGPLFKPENGLLETKVYFAGFPRKVESELIKPINPRLDGCIRSWNLMKQGASGIKEIIQEKQNKHCLVTVEKGSYYPGSGIAQFHIDYNNVSSAEGWHVNVTLNIRPSTGTGVMLALVSGNNTVPFAVSLVDSTSEKSQDILLSVENTVIYRIQALSLCSDQQSHLEFRVNRNNLELSTPLKIETISHEDLQRQLAVLDKAMKAKVATYLGGLPDVPFSATPVNAFYNGCMEVNINGVQLDLDEAISKHNDIRAHSCPSVWKKTKNS

  • Protein Length

    Full Length of Mature Protein

  • Molecular Weight

    78-98 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

PROS1, or Protein S, is a vitamin K-dependent plasma glycoprotein that plays a crucial role in the regulation of coagulation and anticoagulation processes. It is primarily synthesized in the liver and is essential for the proper functioning of the protein C pathway, which is vital for maintaining hemostatic balance. The study of PROS1 has garnered significant attention due to its involvement in various thrombotic disorders and its potential implications in other pathological conditions, including cancer and inflammatory diseases. Mutations in the PROS1 gene can lead to Protein S deficiency, resulting in an increased risk of thrombosis. Research on recombinant PROS1 (rPROS1) has advanced to explore its therapeutic potential, particularly in treating patients with Protein S deficiency. Advances in recombinant DNA technology have enabled the production of rPROS1, allowing for large-scale production and characterization of the protein. Studies have focused on optimizing its expression systems, enhancing stability, and assessing its functional activity in comparison to native Protein S. The development of rPROS1 could provide new avenues for the treatment of clotting disorders, contributing to the management of conditions associated with impaired anticoagulant pathways. As the understanding of PROS1's role in hemostasis deepens and the methodologies for producing recombinant proteins improve, the ongoing research aims to clarify the therapeutic applications of rPROS1 in clinical settings.

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