The protein encoded by this gene is an oxidoreductase that catalyzes the last step in mitochondrial fatty acid synthesis. Defects in this gene are a cause of childhood-onset dystonia and optic atrophy. [provided by RefSeq, Mar 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MECR-20-RE | 20 (40 μL) | 200 μL |  |
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| MECR-20-OR | 20 (40 μL) | 200 μL |  |
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| MECR-20-GO | 20 (40 μL) | 200 μL |  |
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| MECR-20-GR | 20 (40 μL) | 200 μL |  |
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| MECR-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is an oxidoreductase that catalyzes the last step in mitochondrial fatty acid synthesis. Defects in this gene are a cause of childhood-onset dystonia and optic atrophy. [provided by RefSeq, Mar 2017]
Gene Symbol : MECR
Gene Name : Mitochondrial trans-2-enoyl-CoA reductase
Chromosome : CHR 1: 292,309,57-291,926,56
Locus : 1p35.3
Alt. Genes : FEM1B
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