This gene is a member of the mitochondrial carrier family which includes nuclear-encoded transporters localized on the inner mitochondrial membranes. Members of the family transport important small molecules across the mitochondrial inner membrane. This protein is involved in the transport of S-adenosylmethionine (SAM) into the mitochondria. Mutations in this gene are associated with combined oxidative phosphorylation deficiency 28. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC25A26-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC25A26-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC25A26-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC25A26-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC25A26-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a member of the mitochondrial carrier family which includes nuclear-encoded transporters localized on the inner mitochondrial membranes. Members of the family transport important small molecules across the mitochondrial inner membrane. This protein is involved in the transport of S-adenosylmethionine (SAM) into the mitochondria. Mutations in this gene are associated with combined oxidative phosphorylation deficiency 28. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2017]
Gene Symbol : SLC25A26
Gene Name : Solute carrier family 25 member 26
Chromosome : CHR 3: 661,336,09-663,800,20
Locus : 3p14.1
Alt. Genes : FEM1B
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