产品货号：
JN0721
中文名称：
重组人精氨琥珀酸合成酶(ASS1)
英文名称：
Recombinant Human Argininosuccinate Synthase
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-Lys412在N端含有His标签。
ASS1质量控制：＞95%(还原性SDS-PAGE)
ASS1制剂：液体
ASS1保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于ASS1：
Argininosuccinate Synthase (ASS1) is an urea cycle enzyme with a tetrameric structure composed of identical subunits. ASS1 is involved in the synthesis of arginine and catalyzes that condensation of citrulline and aspartate to argininosuccinate using ATP. ASS1 is important to the urea cycle as it catalyzes the important second last step in the arginine biosynthetic pathway. ASS1 mainly expressed in periportal hepatocytes, but also in most other body tissues. A deficiency of ASS1 causes citrullinemia (CTLN1), an autosomal recessive disease which is characterized by severe vomiting spells and mental retardation.
相关搜索：重组人精氨琥珀酸合成酶(ASS1)，Recombinant Human Argininosuccinate Synthase
ASS1质量控制：＞95%(还原性SDS-PAGE)
ASS1制剂：液体
ASS1保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于ASS1：
Argininosuccinate Synthase (ASS1) is an urea cycle enzyme with a tetrameric structure composed of identical subunits. ASS1 is involved in the synthesis of arginine and catalyzes that condensation of citrulline and aspartate to argininosuccinate using ATP. ASS1 is important to the urea cycle as it catalyzes the important second last step in the arginine biosynthetic pathway. ASS1 mainly expressed in periportal hepatocytes, but also in most other body tissues. A deficiency of ASS1 causes citrullinemia (CTLN1), an autosomal recessive disease which is characterized by severe vomiting spells and mental retardation.
相关搜索：重组人精氨琥珀酸合成酶(ASS1)，Recombinant Human Argininosuccinate Synthase