蛋白

重组人类胍基乙酸N-甲基转移酶/GAMT(N, C-6His)

CG67

10微克;50微克;500微克;1毫克

重组蛋白

重组人类胍基乙酸N-甲基转移酶/GAMT(N, C-6His)

重组蛋白

CG67-10微克

10微克;50微克;500微克;1毫克

Q14353

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.

大肠杆菌

Dry ice/Polar packs

Supplied as a 0.2 μm filtered solution of 20mM TrisHCl,1mMDTT,pH 8.0 .

胍基乙酸N-甲基转移酶, GAMT, PIG2, TP53I2