Retinol Dehydrogenase 12 (RDH12) Antibody
357.5€ (100 µg)
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935106861
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name
Retinol Dehydrogenase 12 (RDH12) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx145096
tested applications
ELISA, WB, IHC
Description
Retinol Dehydrogenase 12 (RDH12) Antibody is a Rabbit Polyclonal against Retinol Dehydrogenase 12 (RDH12). The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Retinol Dehydrogenase 12 (RDH12) |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | ELISA: 1/20000 - 1/80000, WB: 1/500 - 1/2000, IHC: 1/100 - 1/200. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Purified by antigen affinity column chromatography. |
| Size 1 | 100 µg |
| Size 2 | 1 mg |
| Form | Lyophilized |
| Tested Applications | ELISA, WB, IHC |
| Buffer | Prior to lyophilization: 1% BSA and 0.02% NaN3. |
| Availability | Shipped within 7-15 working days. |
| Storage | Store at -20 °C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q96NR8 |
| Gene ID | 145226 |
| NCBI Accession | NP_689656.2, NM_152443.2 |
| OMIM | 608830 |
| Background | Antibody anti-RDH12 |
| Status | RUO |
| Note | Concentration: Lyophilized form: Not applicable. After reconstitution: 1 mg/ml. - |
Descripción
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Retinol Dehydrogenase 12 (RDH12) Antibody is a Rabbit Polyclonal against Retinol Dehydrogenase 12 (RDH12). The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53.
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