Solute Carrier Family 25 Member 15 (SLC25A15) Antibody
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Description
SLC25A15 Antibody is a Rabbit Polyclonal antibody against SLC25A15. This gene is a member of the mitochondrial carrier family. The encoded protein transports ornithine across the inner mitochondrial membrane from the cytosol to the mitochondrial matrix. The protein is an essential component of the urea cycle, and functions in ammonium detoxification and biosynthesis of the amino acid arginine. Mutations in this gene result in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. There is a pseudogene of this locus on the Y chromosome.
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Solute Carrier Family 25 Member 15 (SLC25A15) |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | WB: 1/200 - 1/2000. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Purified by affinity chromatography. |
| Size 1 | 60 µl |
| Size 2 | 120 µl |
| Size 3 | 200 µl |
| Form | Liquid |
| Tested Applications | WB |
| Buffer | PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q9Y619 |
| Gene ID | 10166 |
| NCBI Accession | NP_055067.1 |
| Background | Antibody anti-SLC25A15 |
| Status | RUO |
| Note | Concentration: 1 mg/ml - |
Descripción
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SLC25A15 antibody
Ornithine transport across inner mitochondrial membrane, from the cytoplasm to the matrix.
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Solute Carrier Family 25 Member 15 (SLC25A15) Antibody
SLC25A15 Antibody is a Rabbit Polyclonal antibody against SLC25A15. This gene is a member of the mitochondrial carrier family. The encoded protein transports ornithine across the inner mitochondrial membrane from the cytosol to the mitochondrial matrix. The protein is an essential component of the urea cycle, and functions in ammonium detoxification and biosynthesis of the amino acid arginine. Mutations in this gene result in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. There is a pseudogene of this locus on the Y chromosome.
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