RDH5 Polyclonal Antibody (E-AB-53144)
For research use only.
| Verified Samples |
Verified Samples in IHC: Human brain |
| Dilution | IHC 1:50-1:100 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Applications | IHC |
| Clonality | Polyclonal |
| Immunogen | Fusion protein of human RDH5 |
| Abbre | RDH5 |
| Synonyms | 11 cis RDH, 11 cis retinol dehydrogenase, 9 cis retinol specific dehydrogenase, FLJ39337, FLJ97089, HSD17B9, RDH 5, RDH1, Retinol dehydrogenase 1, Retinol dehydrogenase 5, Retinol dehydrogenase 5 (11 cis/9 cis), SDR9C5, Short chain dehydrogenase/reductase family 9C m |
| Swissprot | |
| Cellular Localization | Membrane, Peripheral membrane protein. |
| Concentration | 0.84 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Antigen affinity purification |
| Research Areas | Neuroscience |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
| background | This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S1 (biogenesis of lysosomal organelles complex-1, subunit 1) gene. |
Other Clones
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Other Formats
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Unconjugated
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