The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CPT2BA-20-REGO | 20 (40 μL) | 200 μL |
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| CPT2BA-20-REGR | 20 (40 μL) | 200 μL |
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| CPT2BA-20-ORGR | 20 (40 μL) | 200 μL |
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| CPT2BA-20-GOGR | 20 (40 μL) | 200 μL |
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| CPT2BA-20-GRRE | 20 (40 μL) | 200 μL |
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| CPT2BA-20-GROR | 20 (40 μL) | 200 μL |
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| CPT2BA-20-GRGO | 20 (40 μL) | 200 μL |
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| CPT2BA-20-AQOR | 20 (40 μL) | 200 μL |
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The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders. [provided by RefSeq, Jul 2008]
Gene Symbol : CPT2
Gene Name : Carnitine palmitoyltransferase 2
Chromosome : CHR 1: 531,964,28-532,141,96
Locus : 1p32.3
Alt. Genes : HIPK3
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