SKU: WP16314 Categories: ,

GATM rabbit pAb

Price range: $268.00 through $328.00

SKU: WP16314-100
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Product details

Background:

This gene encodes a mitochondrial enzyme that belongs to the amidinotransferase family. This enzyme is involved in creatine biosynthesis, whereby it catalyzes the transfer of a guanido group from L-arginine to glycine, resulting in guanidinoacetic acid, the immediate precursor of creatine. Mutations in this gene cause arginine:glycine amidinotransferase deficiency, an inborn error of creatine synthesis characterized by mental retardation, language impairment, and behavioral disorders. [provided by RefSeq, Jul 2008],

Specifications

Size50μL/100μL
TargetGATM
ReactivityHuman, Mouse, Rat
ApplicationsWB
MW(Calculated)47kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human GATM AA range: 223-273
SpecificityThis antibody detects endogenous levels of GATM at Human/Mouse/Rat
Gene NameGATM AGAT
Protein NameGATM
Other Name
SpeciesHuman
Gene ID2628
UniprotP50440,
Species.1Mouse
Gene ID.167092
Uniprot.1Q9D964,
Species.2Rat
Gene ID.281660
Uniprot.2P50442
Cellular Localization[Isoform 1]: Mitochondrion inner membrane; Peripheral membrane protein; Intermembrane side. Probably attached to the outer side of the inner membrane.; [Isoform 2]: Cytoplasm.
Tissue ExpressionExpressed in brain, heart, kidney, liver, lung, salivary gland and skeletal muscle tissue, with the highest expression in kidney. Biallelically expressed in placenta and fetal tissues.
Signaling_pathway
Research Areas>>Glycine, serine and threonine metabolism; / >>Arginine and proline metabolism; / >>Metabolic pathways
FunctionCatalytic activity:L-arginine + glycine = L-ornithine + guanidinoacetate.,Disease:Defects in GATM are the cause of L-arginine:glycine amidinotransferase deficiency (AGAT deficiency) [MIM:602360]. AGAT deficiency is a defect in creatine metabolism leading to mental retardation.,Domain:One chain folds into a compact single domain composed of repeating units, five beta-beta-alpha-beta modules, which surround the central active site.,pathway:Amine and polyamine biosynthesis; creatine biosynthesis; creatine from L-arginine and glycine: step 1/2.,similarity:Belongs to the amidinotransferase family.,subcellular location:The mitochondrial form is found in the intermembrane space probably attached to the outer side of the inner membrane.,subunit:Homodimer. There is an equilibrium between the monomeric and dimeric forms, shifted towards the side of the monomer.,tissue specificity:Kidney.,
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