重组视神经萎缩蛋白3

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重组视神经萎缩蛋白3

本产品不向个人销售，仅用作科学研究，不用于任何人体实验及非科研性质的动物实验。

重组视神经萎缩蛋白3(OPA3)
Recombinant OPA3

基因名：

OPA3

产品别名：

MGA3； OPA3； outer mitochondrial membrane lipid metabolism regulator OPA3； outer mitochondrial membrane lipid metabolism regulator OPA3； optic atrophy 3 protein； 3-methylglutaconic aciduria type III； OPA3 outer mitochondrial membrane lipid metabolism regulator； Optic atrophy 3 (Iraqi-Jewish 'optic atrophy plus')； optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)；视神经萎缩蛋白3；视神经萎缩蛋白3(OPA3)；

背景信息：

The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]