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GAMT Recombinant Protein

CAT: 0223-92-194Size: 0.05 mgDry Ice: YesHazardous: No
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CAT#:0223-92-194Size:0.05 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Background
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.
CAS Number
9000-83-3
NCBI Gene ID
2593
Swiss Prot
Q14353
Accession Number
Q14353
Tag
N, C-6 His tag
Type
Recombinant Proteins
Source
E. coli
Buffer
Supplied as a 0.2 um filtered solution of 20mM TrisHCl,1mMDTT, pH 8.0 . It is not recommended to reconstitute to a concentration less than 100 ug/ml.
Shipping Conditions
Dry Ice
Calculated Molecular Weight
29.5 kD
Applications Notes
This recombinant protein can be used for biological assays. For research use only.
NCBI Official Name
Guanidinoacetate N-methyltransferase
NCBI Organism
Homo sapiens
Other Product Names
Guanidinoacetate N-methyltransferase, GAMT, PIG2, TP53I2
Species
Human
Physical Properties
Liquid

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