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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
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; unnamed protein product
基因别名: AdoMet; Ams; MAT; MATA1; SADE; SAMS; SAMS1; SAS
UniProt ID: (Human) Q00266, (Mouse) Q91X83, (Rat) P13444
Entrez Gene ID: (Human) 4143, (Mouse) 11720, (Rat) 25331