产品货号：
JN0953
中文名称：
重组人中链酰基辅酶A脱氢酶(ACADM)(MCAD)
英文名称：
Recombinant Human Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial
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Lys26-Asn421在N端含有His标签。
ACADM质量控制：＞95%(还原性SDS-PAGE)
ACADM制剂：液体
ACADM保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于ACADM：
Medium-Chain Specific Acyl-CoA Dehydrogenase (ACADM) is a mitochondrial fatty acid beta-oxidation that belongs to the acyl-CoA dehydrogenase family. ACADM is a homotetramer enzyme that catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. ACADM is specific for acyl chain lengths of 4 to 16. It is essential for converting these particular fatty acids to energy, especially during fasting periods. Defects in ACADM cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death.
相关搜索：重组人中链酰基辅酶A脱氢酶(ACADM)(MCAD)
ACADM质量控制：＞95%(还原性SDS-PAGE)
ACADM制剂：液体
ACADM保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于ACADM：
Medium-Chain Specific Acyl-CoA Dehydrogenase (ACADM) is a mitochondrial fatty acid beta-oxidation that belongs to the acyl-CoA dehydrogenase family. ACADM is a homotetramer enzyme that catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. ACADM is specific for acyl chain lengths of 4 to 16. It is essential for converting these particular fatty acids to energy, especially during fasting periods. Defects in ACADM cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death.
相关搜索：重组人中链酰基辅酶A脱氢酶(ACADM)(MCAD)