蛋白质/抗原/多肽 >> 重组蛋白
重组甲基丙二酸尿症cblA蛋白
产品介绍 基因名: Mmaa 产品别名: 2810018E08Rik; AI840684; Mmaa; methylmalonic aciduria (cobalamin deficiency) type A; methylmalonic aciduria (cobalamin deficiency) type A; methylmalonic aciduria type A homolog, mitochondrial; 甲基丙二酸尿症cblA; 背景信息: The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria. [provided by RefSeq, Jul 2008]. 标签:His-tag |
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