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Catalog Number | orb1961212 |
---|---|
Category | Small Molecules |
Description | GAMT Protein, Human, Recombinant (His) |
Purity | 98.00% |
MW | 27-32 KDa, reducing conditions |
Biological Activity | 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. |
Note | For research use only |
Expiration Date | 12 months from date of receipt. |
≥90% as determined by SDS-PAGE | |
This protein contains the human GAMT(Met1-Gly236) was fused with the C-terminal His Tag and expressed in E. coli. |
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