产品货号：
JN1057
中文名称：
重组人精氨酸酶1(ARG1)(Arginase-1)
英文名称：
Recombinant Human Arginase-1
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-lys322在C端含有His标签。
Arginase-1/ARG1质量控制：＞95%(还原性SDS-PAGE)
Arginase-1/ARG1制剂：液体
Arginase-1/ARG1保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于Arginase-1/ARG1：
ARG1 is a member of the ureohydrolase family of enzymes. ARG1 can catalyze the hydrolysis of arginine to ornithine and urea. In the urea cycle, ARG1 catalyzes the fifth and final step, a series of biochemical reactions in mammals during which the body disposes of harmful ammonia. ARG1 is a cytosolic enzyme and expressed widely in the liver as part of the urea cycle. Inherited deficiency of this ARG1 causes argininemia, which is an autosomal recessive disorder characterized by hyperammonemia.
相关搜索：重组人精氨酸酶1(ARG1)(Arginase-1)，Recombinant Human Arginase-1
Arginase-1/ARG1质量控制：＞95%(还原性SDS-PAGE)
Arginase-1/ARG1制剂：液体
Arginase-1/ARG1保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于Arginase-1/ARG1：
ARG1 is a member of the ureohydrolase family of enzymes. ARG1 can catalyze the hydrolysis of arginine to ornithine and urea. In the urea cycle, ARG1 catalyzes the fifth and final step, a series of biochemical reactions in mammals during which the body disposes of harmful ammonia. ARG1 is a cytosolic enzyme and expressed widely in the liver as part of the urea cycle. Inherited deficiency of this ARG1 causes argininemia, which is an autosomal recessive disorder characterized by hyperammonemia.
相关搜索：重组人精氨酸酶1(ARG1)(Arginase-1)，Recombinant Human Arginase-1