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GLRA1, Mouse, Clone: 3F1, Abnova™
Mouse monoclonal antibody raised against a partial recombinant GLRA1.
Brand: Abnova H00002741-M05.100ug
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
Sequence: IWKPDLFFANEKGAHFHEITTDNKLLRISRNGNVLYSIRITLTLACPMDLKNFPMDVQTCIMQLESFGYTMNDLIFEWQEQGAVQVADGLTLPQFILKEESpecifications
| GLRA1 | |
| Monoclonal | |
| Unconjugated | |
| PBS with no preservative; pH 7.4 | |
| NM_000171 | |
| GLRA1 | |
| GLRA1 (NP_000162, 121 a.a. ∼ 220 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. | |
| 100 μg | |
| Primary | |
| Human | |
| Antibody | |
| IgG2a κ |
| ELISA, Western Blot | |
| 3F1 | |
| Mouse monoclonal antibody raised against a partial recombinant GLRA1. | |
| GLRA1 | |
| MGC138878/MGC138879/STHE | |
| Mouse | |
| Affinity chromatography | |
| RUO | |
| 2741 | |
| Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. | |
| Liquid |
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