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Recombinant Human GAMT Protein, N-His

Catalog #:   YHG78501 Specific References (49) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: Q14353
Protein length: Val64-Gly236
Overview

Catalog No.

YHG78501

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Val64-Gly236

Predicted molecular weight

22.12 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

Q14353

Applications

ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress

Form

Lyophilized

Storage buffer

Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.

Reconstitution

Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.

Shipping

In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.

Stability and Storage

Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.

Alternative Names

GAMT, Guanidinoacetate N-methyltransferase

Data Image
  • SDS-PAGE
    SDS PAGE for recombinant Human GAMT protein
References

Gene delivery of AGAT and GAMT boosts creatine levels in creatine transporter deficiency patient fibroblasts., PMID:40338959

Experience with gender affirming hormones and puberty blockers (gonadotropin releasing hormone agonist): a qualitative analysis of sexual function., PMID:40192463

GAMT facilitates tumor progression via inhibiting p53 in clear cell renal cell carcinoma., PMID:40176130

[Two cases of creatine deficiency syndrome caused by GAMT gene mutations and literature review]., PMID:40105081

Assessing Creatine-Related Gene Expression in Kidney Disease: Can Available Data Give Insights into an Old Discussion?, PMID:40004980

Effect of gestational age and fetal sex on metabolism of creatine by uteri, placentae, and fetuses of pigs†., PMID:39836382

A creatine efflux transporter in oligodendrocytes., PMID:39792585

Intratesticular creatine maintains spermatogenesis by defining tight junctions., PMID:39730393

Multi-omics analysis and longitudinal study of reprogramming by dietary creatine to endogenous metabolism in largemouth bass (Micropterus salmoides)., PMID:39638990

Gene ontology defines pre-post- hatch energy dynamics in the complexus muscle of broiler chickens., PMID:39633257

Spatial metabolomics highlights metabolic reprogramming in acute myeloid leukemia mice through creatine pathway., PMID:39525575

Establishing a Core Outcome Set for Creatine Transporter Deficiency and Guanidinoacetate Methyltransferase Deficiency., PMID:39371127

Evidence for metabolism of creatine by the conceptus, placenta, and uterus for production of adenosine triphosphate during conceptus development in pigs†., PMID:38836439

Integrated transcriptomics and metabolomics study of embryonic breast muscle of Jiaji ducks., PMID:38824564

ClinGen variant curation expert panel recommendations for classification of variants in GAMT, GATM and SLC6A8 for cerebral creatine deficiency syndromes., PMID:38452609

Role of a novel circRNA-CGNL1 in regulating pancreatic cancer progression via NUDT4-HDAC4-RUNX2-GAMT-mediated apoptosis., PMID:38297362

Evidence of an intracellular creatine-sensing mechanism that modulates creatine biosynthesis via AGAT expression in human HAP1 cells., PMID:38104212

Aspects of human uterine creatine metabolism during the menstrual cycle and at term pregnancy†., PMID:37602666

Evidence and Recommendation for Guanidinoacetate Methyltransferase Deficiency Newborn Screening., PMID:37465909

Fourteen cases of cerebral creatine deficiency syndrome in children: a cohort study in China., PMID:37305710

Creatine Deficiency Disorders: Phenotypes, Genotypes, Diagnosis, and Treatment Outcomes., PMID:36856349

Hepatic oleate regulates one-carbon metabolism during high carbohydrate feeding., PMID:36791500

Guanidinoacetate (GAA) is a potent GABAA receptor GABA mimetic: Implications for neurological disease pathology., PMID:36726215

Creatine metabolism at the uterine-conceptus interface during early gestation in sheep†., PMID:36054379

Influence of homoarginine on creatine accumulation and biosynthesis in the mouse., PMID:36017222

Guanidine acetic acid exhibited greater growth performance in younger (13-30 kg) than in older (30-50 kg) lambs under high-concentrate feedlotting pattern., PMID:35990281

Identification of Genes Predicting Poor Response of Trastuzumab in Human Epidermal Growth Factor Receptor 2 Positive Breast Cancer., PMID:35935587

Processing mechanism of guanidinoacetate in choroid plexus epithelial cells: conversion of guanidinoacetate to creatine via guanidinoacetate N-methyltransferase and monocarboxylate transporter 12-mediated creatine release into the CSF., PMID:35658878

Identification of novel variations in SLC6A8 and GAMT genes causing cerebral creatine deficiency syndrome., PMID:35588794

Creatine nitrate supplementation strengthens energy status and delays glycolysis of broiler muscle via inhibition of LKB1/AMPK pathway., PMID:35007932

Elastic net-based identification of GAMT as potential diagnostic marker for early-stage gastric cancer., PMID:34990904

Cerebral creatine deficiency disorders - A clinical, genetic and follow up study from India., PMID:34974949

Creatine metabolism in patients with urea cycle disorders., PMID:34471603

Intellectual Disability and Brain Creatine Deficit: Phenotyping of the Genetic Mouse Model for GAMT Deficiency., PMID:34440375

GATM and GAMT synthesize creatine locally throughout the mammalian body and within oligodendrocytes of the brain., PMID:34418357

Identification of candidate genomic regions for chicken egg number traits based on genome-wide association study., PMID:34376144

Prognostic Significance of KIF11 and KIF14 Expression in Pancreatic Adenocarcinoma., PMID:34208606

Phosphate Suppression of Arbuscular Mycorrhizal Symbiosis Involves Gibberellic Acid Signaling., PMID:34037236

Identification of Metabolic-Associated Genes for the Prediction of Colon and Rectal Adenocarcinoma., PMID:33833525

A new rat model of creatine transporter deficiency reveals behavioral disorder and altered brain metabolism., PMID:33452333

Cardiac expression and location of hexokinase changes in a mouse model of pure creatine deficiency., PMID:33337958

[Genetic analysis and treatment for an infant with cerebral creatine deficiency syndrome type 2]., PMID:32820516

Inhibition of myostatin prevents microgravity-induced loss of skeletal muscle mass and strength., PMID:32315311

Exploring the protective effects of schizandrol A in acute myocardial ischemia mice by comprehensive metabolomics profiling integrated with molecular mechanism studies., PMID:32123298

Age-Dependent Decline in Cardiac Function in Guanidinoacetate-N-Methyltransferase Knockout Mice., PMID:32038270

The Effects of Early-Onset Pre-Eclampsia on Placental Creatine Metabolism in the Third Trimester., PMID:31991880

Magnetic resonance imaging reveals specific anatomical changes in the brain of Agat- and Gamt-mice attributed to creatine depletion and guanidinoacetate alteration., PMID:31951021

Muscle phenotype of AGAT- and GAMT-deficient mice after simvastatin exposure., PMID:31853708

A novel mutation in two cousins with guanidinoacetate methyltransferase (GAMT) deficiency presented with autism., PMID:31559727

Datasheet
$ 313
Product specifications
100 μg 313 1 mg 1629

Contact Information

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For research use only. Not for human or drug use.

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Recombinant Human GAMT Protein, N-His [YHG78501]
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