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Antibody detects endogenous levels of total ME2.
ME2 encodes a mitochondrial NAD-dependent malic enzyme, a homotetrameric protein, that catalyzes the oxidative decarboxylation of malate to pyruvate. It had previously been weakly linked to a syndrome known as Friedreich ataxia that has since been shown to be the result of mutation in a completely different gene. Certain single-nucleotide polymorphism haplotypes of this gene have been shown to increase the risk for idiopathic generalized epilepsy. Alternatively spliced transcript variants encoding different isoforms found for this gene.
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: malate dehydrogenase; malate dehydrogenase (oxaloacetate-decarboxylating); Malic enzyme 2; malic enzyme 2, NAD(+)-dependent, mitochondrial; NAD-dependent malic enzyme, mitochondrial; NAD-ME; pyruvic-malic carboxylase
基因别名: AW120568; D030040L20Rik; ME2; NAD-ME; ODS1
UniProt ID: (Human) P23368, (Mouse) Q99KE1
Entrez Gene ID: (Human) 4200, (Mouse) 107029