GAMT Protein, Human, Recombinant (His)
Ref. TM-TMPJ-01114
| 1mg | 2,591.00 € | ||
| 10µg | 121.00 € | ||
| 50µg | 353.00 € | ||
| 500µg | 1,803.00 € |
Product Information
- Guanidinoacetate N-methyltransferase, TP53I2, PIG2, 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.
Chemical properties
Technical inquiry about: TM-TMPJ-01114 GAMT Protein, Human, Recombinant (His)
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