Cat: PA1000-8810

Recombinant Human PXR Protein,His

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关键信息

  • 基因名

    PXR

  • 应用

    SPRMSTBLIITCELISA细胞实验药物筛选

  • 别名

    PXR;PXR;Nuclear receptor subfamily 1 group I member 2

  • 种属

    Human

  • 表达系统

    E. coli

  • 标签

    His tag N-Terminus

  • 纯度

    Greater than 90% as determined by SDS-PAGE.

  • 蛋白编号

    O75469

  • 表达区间

    1-434aa

  • 氨基酸序列

    MEVRPKESWNHADFVHCEDTESVPGKPSVNADEEVGGPQICRVCGDKATGYHFNVMTCEGCKGFFRRAMKRNARLRCPFRKGACEITRKTRRQCQACRLRKCLESGMKKEMIMSDEAVEERRALIKRKKSERTGTQPLGVQGLTEEQRMMIRELMDAQMKTFDTTFSHFKNFRLPGVLSSGCELPESLQAPSREEAAKWSQVRKDLCSLKVSLQLRGEDGSVWNYKPPADSGGKEIFSLLPHMADMSTYMFKGIISFAKVISYFRDLPIEDQISLLKGAAFELCQLRFNTVFNAETGTWECGRLSYCLEDTAGGFQQLLLEPMLKFHYMLKKLQLHEEEYVLMQAISLFSPDRPGVLQHRVVDQLQEQFAITLKSYIECNRPQPAHRFLFLKIMAMLTELRSINAQHTQRLLRIQDIHPFATPLMQELFGITGS

  • 分子量

    69.8kDa

  • 内毒素

    < 1.0 EU per μg protein as determined by the LAL method.

  • 性状

    Freeze-dried powder

  • 缓冲液

    PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.

  • 复溶方法

    Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.

  • 个性化定制

    点位突变 标签定制 buffer定制 全长蛋白定制

  • 稳定性测试

    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.

  • 保存条件 & 期限

    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.

  • 运输条件

    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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背景信息

PXR (Pregnane X Receptor) is a nuclear receptor that plays a crucial role in the regulation of xenobiotic metabolism and drug detoxification processes in the liver. Initially identified as a receptor activated by steroid hormones, PXR has garnered significant attention due to its ability to modulate the expression of various drug-metabolizing enzymes, particularly cytochrome P450 isoforms, and transport proteins. The relevance of PXR in pharmacology is underscored by its involvement in drug-drug interactions and variable drug responses among individuals. Research into PXR has expanded to include its potential role in diseases such as liver disorders, cancer, and metabolic syndromes. Moreover, PXR is also being explored as a therapeutic target to enhance drug efficacy and minimize adverse effects through its modulation. The development of recombinant PXR proteins for structural and functional studies has provided valuable insights into its ligand-binding mechanisms and the downstream signaling pathways it influences. These recombinant proteins serve as essential tools for understanding PXR's interactions with various ligands and for screening potential agonists or antagonists, thereby contributing to the advancement of personalized medicine and improving therapeutic strategies involving drugs that undergo PXR-mediated metabolism. Overall, the ongoing research into PXR and its recombinant proteins is pivotal for uncovering novel insights into drug metabolism and the pharmacological implications associated with this important nuclear receptor.

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