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Antibody detects endogenous levels of total MAT1A.
MAT1A catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.This gne encodes methionine adenosyltransferase I (alpha isoform), which catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: AdoMet synthase 1; adoMet synthetase 1; MAT 1; MAT-I/III; Methionine adenosyltransferase 1; methionine adenosyltransferase I, alpha; Methionine adenosyltransferase I/III; S - adenosylmethionine synthetase; S-adenosylmethionine synthase isoform type-1; S-adenosylmethionine synthetase isoform type-1
基因别名: AdoMet; AI046368; Ams; AMS1; MAT; MAT1A; MATA1; SADE; SAMS; SAMS1; SAS
UniProt ID: (Human) Q00266, (Rat) P13444, (Mouse) Q91X83
Entrez Gene ID: (Human) 4143, (Rat) 25331, (Mouse) 11720