GLRA1 Polyclonal Antibody Store at -20°C
SKU: E-AB-16153-200
GLRA1 Polyclonal Antibody Store at -20°C
| SKU # | E-AB-16153 |
| Reactivity | Human, Mouse, Rat |
| Host | Rabbit |
| Applications | WB, IHC |
Product Details
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Applications | WB, IHC |
| Clonality | Polyclonal |
| Immunogen | Synthetic peptide of human GLRA1 |
| Abbre | GLRA1 |
| Synonyms | GLRA1, Glycine receptor, Glycine receptor 48 kDa subunit, Glycine receptor alpha 1, Glycine receptor strychnine-binding subunit, Glycine receptor subunit alpha-1, HKPX1, STHE, alpha 1 subunit |
| Swissprot | |
| Calculated MW | 53 kDa |
| Cellular Localization | Cell junction>synapse>postsynaptic cell membrane. Cell membrane. |
| Concentration | 0.2 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Neuroscience |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
Related Reagents
| Applications | Recommended Dilution |
| WB | 1:500-1:2000 |
| IHC | 1:25-1:100 |
Background
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.