Cat: IPD-X41392

Recombinant Human NR2F1 Protein ,His

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Analytical Data

  • Gene name

    NR2F1

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    (COUP-TF1)(COUP transcription factor I)(COUP-TF I)(Nuclear receptor subfamily 2 group F member 1)(V-erbA-related protein 3)(EAR-3)

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- His

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P10589

  • Expression Region

    1-423aa

  • Molecular Weight

    50.2 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

NR2F1, also known as nuclear receptor subfamily 2 group F member 1, is a transcription factor that plays a critical role in various biological processes, including development and differentiation of the central nervous system, as well as the regulation of metabolic pathways. Mutations or dysregulation of NR2F1 have been linked to several developmental disorders, including cognitive impairment and phenotypic abnormalities. Given its significant impact on embryonic development and cellular regulation, NR2F1 has garnered attention in both basic and translational research. The production of recombinant NR2F1 protein allows researchers to investigate its functional properties, binding mechanisms, and interactions with other nuclear receptors and co-factors. This can provide insights into its regulatory roles in gene expression and highlight potential therapeutic targets for associated diseases. Additionally, studying NR2F1's structure-function relationships through recombinant protein approaches can elucidate its involvement in diverse physiological processes and pave the way for novel interventions aimed at disorders stemming from its dysfunction. As a result, the research surrounding NR2F1 recombinant protein not only sheds light on fundamental biological questions but also holds promise for advancing therapeutic strategies in developmental and metabolic disorders.

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