GATM Mouse Monoclonal Antibody [Kloon ID: LBI1C9]

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]

Carrier-free (BSA/glycerol-free) GATM mouse monoclonal antibody, clone LBI1C9

AGAT; AT; CCDS3

Homo sapiens glycine amidinotransferase (GATM), transcript variant 1, mRNA; nuclear gene for mitochondrial product.

2628

P50440

Unconjugated

Arginine and proline metabolism, Glycine, serine and threonine metabolism, Metabolic pathways

Arginine and proline metabolism, Glycine, serine and threonine metabolism, Metabolic pathways

WB 1:500~2000, IHC 1:150, IF 1:100, FLOW 1:100

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

GATM

https://www.ncbi.nlm.nih.gov/gene/?term=2628

https://www.uniprot.org/uniprot/P50440