Retinol Dehydrogenase 12 (RDH12) Antibody (FITC)
169€ (20 µg)
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name
Retinol Dehydrogenase 12 (RDH12) Antibody (FITC)
category
Primary Antibodies
provider
Abbexa
reference
abx309613
Description
Retinol Dehydrogenase 12 (RDH12) Antibody (FITC) is a Rabbit Polyclonal against Retinol Dehydrogenase 12 (RDH12) conjugated to FITC. 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 | Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | FITC |
| Isotype | IgG |
| Purity | > 95% |
| Purification | Purified by Protein G. |
| Size 1 | 20 µg |
| Size 2 | 50 µg |
| Size 3 | 100 µg |
| Size 4 | 200 µg |
| Size 5 | 1 mg |
| Form | Liquid |
| Buffer | 0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% Glycerol. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid exposure to light. 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: 0.25 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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