This gene encodes a member of the ferredoxin family. The encoded protein contains a 2Fe-2S ferredoxin-type domain and is essential for heme A and Fe/S protein biosynthesis. Mutation in FDX1L gene is associated with mitochondrial muscle myopathy. [provided by RefSeq, Sep 2014]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FDX1L-20-RE | 20 (40 μL) | 200 μL |  |
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| FDX1L-20-OR | 20 (40 μL) | 200 μL |  |
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| FDX1L-20-GO | 20 (40 μL) | 200 μL |  |
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| FDX1L-20-GR | 20 (40 μL) | 200 μL |  |
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| FDX1L-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the ferredoxin family. The encoded protein contains a 2Fe-2S ferredoxin-type domain and is essential for heme A and Fe/S protein biosynthesis. Mutation in FDX1L gene is associated with mitochondrial muscle myopathy. [provided by RefSeq, Sep 2014]
Gene Symbol : FDX1L
Gene Name : Ferredoxin 1 like
Chromosome : CHR 19: 103,160,14-103,102,10
Locus : 19p13.2
Alt. Genes : ABI2
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