Recombinant Human UPB1 (C-6His)

Recombinant Human UPB1 (C-6His

)
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  • ¥1080 - 11000
  • EnkiLife
  • PEH0174
  • 2025年10月22日
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    • 详细信息
    • 技术资料
    • 英文名

      BUP-1/UPB1/β-ureidopropionase

    • 供应商

      武汉恩玑生命科技有限公司

    • 规格

      10ug/50ug/500ug

    规格:10ug产品价格:¥1080.0
    规格:50ug产品价格:¥3180.0
    规格:500ug产品价格:¥11000.0
    产品名称

    Recombinant Human UPB1 (C-6His)

    英文名称

    BUP-1/UPB1/β-ureidopropionase  

    纯度

    Greater than 95% as determined by reducing SDS-PAGE

    内毒素

    <1 EU/µg as determined by LAL test.

    蛋白构建

    Recombinant Human Beta-Ureidopropionase is produced by our E.coli expression system and the target gene encoding Met1-Glu384 is expressed with a 6His tag at the C-terminus.

    Accession

    Q9UBR1

    表达宿主

    E.coli

    种属

    Human

    预测分子量

    44.22 KDa

    制剂

    Supplied as a 0.2 μm filtered solution of PBS, pH 7.4.

    运输方式

    The product is shipped on dry ice/polar packs.Upon receipt, store it immediately at the temperature listed below.

    稳定性&储存

    Store at ≤-70°C, stable for 6 months after receipt.Store at ≤-70°C, stable for 3 months under sterile conditions after opening. Please minimize freeze-thaw cycles.

    复溶

     

    分子别名
    Beta-Ureidopropionase; BUP-1; Beta-Alanine Synthase; N-Carbamoyl-Beta-Alanine Amidohydrolase; UPB1; BUP1

     

    背景介绍
    β-Ureidopropionase is a cytoplasmic protein which belongs to the CN hydrolase family of BUP subfamily. β-Ureidopropionase binds one zinc ion per subunit, catalyzes the last step in the pyrimidine degradation pathway. β-Ureidopropionase can convert N-carbamyl-beta-aminoisobutyric acid and N-carbamyl-beta-alanine to beta-aminoisobutyric acid and beta-alanine, ammonia and carbon dioxide, respectively. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidine dehydrogenase (DHPDH), dihydropyrimidinase (DHP) and beta-ureidopropionase (UP) to beta-alanine and beta aminoisobutyric acid, respectively. Defects in β-Ureidopropionase are the cause of β-Ureidopropionase deficiency that is characterized by muscular hypotonia, dystonic movements, scoliosis, microcephaly and severe developmental delay.

     

    注意事项

    本司产品仅用于科研,不用于临床诊断和治疗

     

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    Recombinant Human UPB1 (C-6His)
    ¥1080 - 11000