产品货号:
JN1985
中文名称:
重组人β-脲基丙酸酶
英文名称:
Recombinant Human beta-Ureidopropionase
产品规格:
10μg|50μg|500μg|1mg
发货周期:
1~3天
产品价格:
询价
本品由我们的大肠杆菌表达系统制备而成,目的基因编码的Met1-Glu384在C端含有His标签。
β-Ureidopropionase质量控制:>95%(还原性SDS-PAGE)
β-Ureidopropionase制剂:液体
β-Ureidopropionase保存:收到货后请置于-20℃,可保存6个月,避免反复冻融。
关于β-Ureidopropionase:
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.
相关搜索:重组人β-脲基丙酸酶,Recombinant Human beta-Ureidopropionase
β-Ureidopropionase质量控制:>95%(还原性SDS-PAGE)
β-Ureidopropionase制剂:液体
β-Ureidopropionase保存:收到货后请置于-20℃,可保存6个月,避免反复冻融。
关于β-Ureidopropionase:
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.
相关搜索:重组人β-脲基丙酸酶,Recombinant Human beta-Ureidopropionase