产品货号：
JN1050
中文名称：
重组人GAMT(胍基乙酸N-甲基转移酶)
英文名称：
Recombinant Human Guanidinoacetate N-methyltransferase
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-Gly236在N端、C端都带有His标签。
GAMT质量控制：＞95%(还原性SDS-PAGE)
GAMT制剂：液体
GAMT保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于GAMT：
GAMT is a methyltransferase which belongs to the class I-like SAM-binding methyltransferase superfamily. It contains one RMT2 (arginine N-methyltransferase 2-like) domain and is expressed in liver. GAMT converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Defects in GAMT are the cause of guanidinoacetate methyltransferase deficiency, which is an autosomal recessive disorder characterized by developmental delay/regression, mental retardation, severe disturbance of expressive and cognitive speech, intractable seizures and movement disturbances, severe depletion of creatine/phosphocreatine in the brain, and accumulation of guanidinoacetic acid in brain and body fluids.
相关搜索：重组人GAMT(胍基乙酸N-甲基转移酶)
GAMT质量控制：＞95%(还原性SDS-PAGE)
GAMT制剂：液体
GAMT保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于GAMT：
GAMT is a methyltransferase which belongs to the class I-like SAM-binding methyltransferase superfamily. It contains one RMT2 (arginine N-methyltransferase 2-like) domain and is expressed in liver. GAMT converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Defects in GAMT are the cause of guanidinoacetate methyltransferase deficiency, which is an autosomal recessive disorder characterized by developmental delay/regression, mental retardation, severe disturbance of expressive and cognitive speech, intractable seizures and movement disturbances, severe depletion of creatine/phosphocreatine in the brain, and accumulation of guanidinoacetic acid in brain and body fluids.
相关搜索：重组人GAMT(胍基乙酸N-甲基转移酶)