Cat: PA2000-2072

Recombinant Human L2HGDH Protein,His

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关键信息

  • 基因名

    L2HGDH

  • 应用

    SPRMSTBLIITCELISA细胞实验药物筛选

  • 别名

    L2HGDH;C14orf160;L-2-hydroxyglutarate dehydrogenase. mitochondrial

  • 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

    Q9H9P8

  • 表达区间

    52-463aa

  • 氨基酸序列

    VIVGGGIVGLASARALILRHPSLSIGVLEKEKDLAVHQTGHNSGVIHSGIYYKPESLKAKLCVQGAALLYEYCQQKGISYKQCGKLIVAVEQEEIPRLQALYEKGLQNGVPGLRLIQQEDIKKKEPYCRGLMAIDCPHTGIVDYRQVALSFAQDFQEAGGSVLTNFEVKGIEMAKESPSRSIDGMQYPIVIKNTKGEEIRCQYVVTCAGLYSDRISELSGCTPDPRIVPFRGDYLLLKPEKCYLVKGNIYPVPDSRFPFLGVHFTPRMDGSIWLGPNAVLAFKREGYRPFDFSATDVMDIIINSGLIKLASQNFSYGVTEMYKACFLGATVKYLQKFIPEITISDILRGPAGVRAQALDRDGNLVEDFVFDAGVGDIGNRILHVRNAPSPAATSSIAISGMIADEVQQRFEL

  • 分子量

    61.3kDa

  • 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.

质检流程

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背景信息

L2HGDH (L-2-hydroxyglutarate dehydrogenase) is an essential enzyme involved in the metabolism of L-2-hydroxyglutarate (2-HG), a metabolite that has gained attention due to its association with various neurological disorders and certain types of cancers, particularly gliomas. Mutations in the L2HGDH gene can lead to a rare metabolic disorder known as L-2-hydroxyglutaric aciduria, which is characterized by elevated levels of 2-HG in the body, resulting in neurological symptoms and developmental issues. Research into the recombinant production of L2HGDH protein seeks to elucidate its biochemical properties, functional mechanisms, and potential therapeutic applications. By utilizing recombinant DNA technology, scientists can produce large quantities of this enzyme, allowing for detailed studies on its enzymatic activity, structure-function relationships, and interactions with substrates and inhibitors. Furthermore, understanding the role of L2HGDH in cellular metabolism and its implications in disease processes could pave the way for innovative diagnostic and treatment strategies for conditions associated with dysregulation of 2-HG levels. The quest for effective therapies targeting L2HGDH and the pathways it influences has become increasingly relevant in precision medicine, as the knockdown of this enzyme has shown potential in altering metabolic profiles that drive tumorigenesis. Therefore, the study of recombinant L2HGDH not only contributes to basic biological knowledge but also has significant implications for the development of novel therapeutic approaches in oncology and neurology.

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