Guanidinoacetate N-Methyltransferase (GAMT) ELISA Kits

The protein encoded by GAMT is a methyltransferase that converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Additionally we are shipping GAMT Antibodies (71) and GAMT Proteins (23) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
GAMT 14431 O35969
GAMT 2593 Q14353
GAMT 25257  
How to order from antibodies-online
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Order online

Top GAMT ELISA Kits at

Showing 4 out of 5 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Delivery Price Details
Rat 9.77 pg/mL 39.07-2500 pg/mL Typical standard curve 96 Tests 15 to 18 Days
  96 Tests 15 to 18 Days
  96 Tests 15 to 18 Days
  96 Tests 15 to 18 Days

More ELISA Kits for GAMT Interaction Partners

Mouse (Murine) Guanidinoacetate N-Methyltransferase (GAMT) interaction partners

  1. Inactivation of the creatine kinase system by GAMT deficiency does not alter mitochondrial organization and intracellular compartmentation in relaxed cardiomyocytes.

  2. GAMT was expressed highly in oligodendrocytes and olfactory ensheathing glia and moderately in astrocytes, whereas GAMT was very low in neurons and microglia.

  3. despite the absence of Cr, GAMT-/- mice can cope with mild ischaemic stress by using phosphorylated guanidinoacetate for high energy phosphoryl transfer

  4. GAMT(Cr)-/- mice showed differences in maximal rates of force rise and relaxation times during the isometric protocol as well as in force during the dynamic protocol.

  5. Our results can provide the basis for additional experiments to optimize Cr supplementation in GAMT deficiency, as increases in brain Cr are slow in patients after Cr supplementation.

  6. GAMT and AGAT mRNA are up-regulated 5.4- and 1.9-fold respectively in adult mdx muscle compared to C57

  7. In the fetal brain, mRNA expression of GAMT was relatively low until 34 days gestation (term is 38-39 days). In the fetal kidney and liver, GAMT mRNA and protein expression were also relatively low until 34-37 days gestation.

Human Guanidinoacetate N-Methyltransferase (GAMT) interaction partners

  1. We unveil PFN2 and GAMT as molecular determinants of Charcot-Marie-Tooth type 2 neuropathy, with possible indications of the role of PFN2 in the pathogenesis and disease progression.

  2. Measurements of creatine and guanidinoacetate in plasma are recommended for the diagnosis of AGAT and GAMT deficiency.Definitive confirmation of the diagnosis requires DNA sequencing of the appropriate gene and (if molecular analysis is ambiguous) measurement of AGAT or GAMT enzyme activity or of CRTR-mediated transport

  3. Data suggest that creatine is provided equally by diet and by endogenous synthesis from arginine and glycine with successive involvement of arginine glycine amidinotransferase [AGAT] and guanidinoacetate methyl transferase [GAMT]. [REVIEW]

  4. As early diagnosis results in normal neurodevelopmental outcome, GAMT deficiency should be included in newborn screening programs to diagnose individuals at the asymptomatic stage of the disease

  5. The estimated incidence of GAMT deficiency is 1:250,000 newborns based on our pilot study.

  6. Study reports six novel pathogenic mutations in GAMT gene in patients with Guanidinoacetate methyltransferase deficiency.

  7. Two novel heterozygous variants with sequence deletion and sequence insertion in the GAMT gene have been identified in newborns with guanidinoacetate methyltransferase deficiency.

  8. impact of creatine deficiency syndrome mutations, CRTR and GAMT on metabolic stress was analyzed in patient fibroblast cultures

  9. GAMT genes may not be directly involved in human male infertility

  10. Mutations in the GAMT gene are responsible for GAMT deficiency, since overexpression of the GAMT open reading frame restores GAMT activity in GAMT-deficient fibroblasts.

  11. compound heterozygous mutations in the GAMT gene may be causitive in guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathy [case report]

  12. the carrier rate of the c.59G>C; p.Trp20Ser mutation in GAMT is relatively high in these islands, as well as in other parts of Portugal.

  13. Five novel mutations were identified in GAMT from 8 patients with GAMT deficiency.

  14. Body fluids from 10 GAMT deficient patients were analysed using (1)H NMR spectroscopy.

Zebrafish Guanidinoacetate N-Methyltransferase (GAMT) interaction partners

  1. The spatiotemporal expression pattern of gamt during zebrafish embryogenesis was revealed.

GAMT Antigen Profile

Antigen Summary

The protein encoded by this gene is a methyltransferase that converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Defects in this gene have been implicated in neurologic syndromes and muscular hypotonia, probably due to creatine deficiency and accumulation of guanidinoacetate in the brain of affected individuals. Two transcript variants encoding different isoforms have been described for this gene. Pseudogenes of this gene are found on chromosomes 2 and 13.

Gene names and symbols associated with GAMT

  • guanidinoacetate N-methyltransferase (gamt) antibody
  • guanidinoacetate N-methyltransferase (GAMT) antibody
  • guanidinoacetate methyltransferase (Gamt) antibody
  • guanidinoacetate N-methyltransferase (Gamt) antibody
  • AA571402 antibody
  • CCDS2 antibody
  • GAMT antibody
  • GMT antibody
  • MGC75698 antibody
  • PIG2 antibody
  • Spintz1 antibody
  • TP53I2 antibody
  • zgc:123136 antibody

Protein level used designations for GAMT

guanidinoacetate N-methyltransferase , Guanidinoacetate N-methyltransferase , guanidinoacetate methyltransferase

394491 Xenopus (Silurana) tropicalis
485085 Canis lupus familiaris
749982 Pan troglodytes
770737 Gallus gallus
100196494 Salmo salar
100528342 Ictalurus punctatus
14431 Mus musculus
2593 Homo sapiens
515270 Bos taurus
25257 Rattus norvegicus
796865 Danio rerio
Selected quality suppliers for GAMT (GAMT) ELISA Kits
Did you look for something else?