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Description
The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor. The receptor mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Two transcript variants encoding different isoforms have been found for this gene
Specifications
Specifications
| Antigen | GLRA1 |
| Applications | ELISA, Western Blot |
| Classification | Monoclonal |
| Clone | 2G4 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against a partial recombinant GLRA1. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | GLRA1 |
| Gene Accession No. | NM_000171 |
| Gene Alias | MGC138878/MGC138879/STHE |
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