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重组甲基丙二酸尿症cblA蛋白
产品名称 Recombinant Mmaa Recombinant methylmalonic aciduria (cobalamin deficiency) type A protein 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]. |
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