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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 | Polyclonal |
| Conjugate | Unconjugated |
| Description | Rabbit polyclonal antibody raised against synthetic peptide of GLRA1. |
| Dilution | ELISA (1:16000-1:60000) Western Blot (1:200-1000) The optimal working dilution should be determined by the end user. |
| Formulation | In serum (0.02% sodium azide) |
| Gene | GLRA1 |
| Gene Accession No. | P23415 |
| Gene Alias | MGC138878/MGC138879/STHE |
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