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Description
This gene product is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. It is a component of the mitochondrial network. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
Specifications
Specifications
| Antigen | OPA1 |
| Applications | ELISA |
| Classification | Monoclonal |
| Clone | 1C10 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against a partial recombinant OPA1. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | OPA1 |
| Gene Accession No. | NM_015560 |
| Gene Alias | FLJ12460/KIAA0567/MGM1/NPG/NTG/largeG |
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