Cat: PA2000-9764

Recombinant Human NPAS2 Protein,GST

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关键信息

  • 基因名

    NPAS2

  • 应用

    SPRMSTBLIITCELISA细胞实验药物筛选

  • 别名

    Basic helix loop helix PAS protein MOP4; Basic-helix-loop-helix-PAS protein MOP4; bHLHe9; class E basic helix loop helix protein 9; Class E basic helix-loop-helix protein 9; FLJ23138; Member of PAS protein 4; Member of PAS superfamily 4; MGC71151; MOP4; Neuronal PAS domain containing protein 2; Neuronal PAS domain protein 2; Neuronal PAS domain-containing protein 2; Neuronal PAS2; NPAS2; NPAS2_HUMAN; PAS domain containing protein 4; PAS domain-containing protein 4; PASD4

  • 种属

    Human

  • 表达系统

    E. coli

  • 标签

    GST-tag at N-terminal

  • 纯度

    Greater than 90% as determined by SDS-PAGE.

  • 蛋白编号

    Q99743

  • 表达区间

    1-824  aa

  • 氨基酸序列

    MDEDEKDRAKRASRNKSEKKRRDQFNVLIKELSSMLPGNTRKMDKTTVLEKVIGFLQKHNEVSAQTEICDIQQDWKPSFLSNEEFTQLMLEALDGFIIAVTTDGSIIYVSDSITPLLGHLPSDVMDQNLLNFLPEQEHSEVYKILSSHMLVTDSPSPEYLKSDSDLEFYCHLLRGSLNPKEFPTYEYIKFVGNFRSYNNVPSPSCNGFDNTLSRPCRVPLGKEVCFIATVRLATPQFLKEMCIVDEPLEEFTSRHSLEWKFLFLDHRAPPIIGYLPFEVLGTSGYDYYHIDDLELLARCHQHLMQFGKGKSCCYRFLTKGQQWIWLQTHYYITYHQWNSKPEFIVCTHSVVSYADVRVERRQELALEDPPSEALHSSALKDKGSSLEPRQHFNALDVGASGLNTSHSPSASSRSSHKSSHTAMSEPTSTPTKLMAEASTPALPRSATLPQELPVPGLSQAATMPAPLPSPSSCDLTQQLLPQTVLQSTPAPMAQFSAQFSMFQTIKDQLEQRTRILQANIRWQQEELHKIQEQLCLVQDSNVQMFLQQPAVSLSFSSTQRPEAQQQLQQRSAAVTQPQLGAGPQLPGQISSAQVTSQHLLRESSVISTQGPKPMRSSQLMQSSGRSGSSLVSPFSSATAALPPSLNLTTPASTSQDASQCQPSPDFSHDRQLRLLLSQPIQPMMPGSCDARQPSEVSRTGRQVKYAQSQTVFQNPDAHPANSSSAPMPVLLMGQAVLHPSFPASQPSPLQPAQARQQPPQHYLQVQAPTSLHSEQQDSLLLSTYSQQPGTLGYPQPPPAQPQPLRPPRRVSSLSESSGLQQPPR

  • 分子量

    118.2 kDa

  • 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

NPAS2 (Neuronal PAS Domain Protein 2) is a member of the PAS family of proteins and plays a crucial role in the regulation of circadian rhythms and neurobiology. This transcription factor is primarily expressed in the brain and is essential for the synchronization of circadian cycles with environmental cues. Dysregulation of NPAS2 has been linked to various neuropsychiatric disorders, including depression and bipolar disorder. Researchers have shown that NPAS2 interacts with several signaling pathways, influencing gene expression related to circadian rhythms and neuronal function. Given its pivotal role in maintaining circadian homeostasis, recombinant NPAS2 protein has become a focus of study for better understanding its functions and potential therapeutic targets. By producing NPAS2 as a recombinant protein, scientists can investigate its structural characteristics, binding interactions, and regulatory mechanisms in a controlled environment. This research is vital, as it may lead to novel interventions for circadian-related disorders and further elucidate the complex biology of neuronal signaling and behavior. The study of NPAS2, particularly in its recombinant form, provides valuable insights into the molecular underpinnings of circadian clock regulation and offers promising avenues for future therapeutic development.

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