SLC25A38 Rabbit pAb
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This gene is a member of the mitochondrial carrier family. The encoded protein is required during erythropoiesis and is important for the biosynthesis of heme. Mutations in this gene are the cause of autosomal congenital sideroblastic anemia (anemia, sideroblastic, 2, pyridoxine-refractory). A related pseudogene is found on chromosome 1.

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推荐稀释比 WB:1/500-1/1000;IF:1:50/1:200
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-25 ~ -15℃保存,收到货之后有效期1年,避免反复冻融。

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