Description
Size quantity : 1-EA
Description : 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.
$94.99
application (WB, IHC-P, ELISA) & cross reactivity (Human, Mouse, Rat)
| Weight | 1.00 lbs |
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| Dimensions | 5.00 × 5.00 × 5.00 in |
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Size quantity : 1-EA
Description : 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.