Reactive species
                            
                                Human;Mouse;Rat                            
                         
                                                
                                                
                                                
                                                
                            Protein name
                            
                                Gamma-aminobutyric acid receptor subunit alpha-1                            
                         
                                                
                                                
                            Immunogen
                            
                                The antiserum was produced against synthesized peptide derived from the Internal region of human GABRA1. AA range:61-110                            
                         
                                                
                            Specificity
                            
                                GABAA Rα1 Monoclonal Antibody detects endogenous levels of GABAA Rα1 protein.                            
                         
                                                
                            Constitute
                            
                                Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.                            
                         
                                                
                            Source
                            
                                Monoclonal, Mouse,IgG                            
                         
                                                
                            Dilution rate
                            
                                WB: 1/500 - 1/2000                            
                         
                                                
                            Purification process
                            
                                The antibody was affinity-purified from mouse antiserum by affinity-chromatography using epitope-specific immunogen.                            
                         
                                                
                                                
                                                
                            Other name
                            
                                GABRA1; Gamma-aminobutyric acid receptor subunit alpha-1; GABA(A) receptor subunit alpha-1                            
                         
                                                
                            Background
                            
                                This gene encodes a gamma-aminobutyric acid (GABA) receptor. GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. GABA-A receptors are pentameric, consisting of proteins from several subunit classes: alpha, beta, gamma, delta and rho. Mutations in this gene cause juvenile myoclonic epilepsy and childhood absence epilepsy type 4. Multiple transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008],                            
                         
                                                
                            Function
                            
                                disease:Defects in GABRA1 are a cause of juvenile myoclonic epilepsy (EJM) [MIM:606904]. EJM is a subtype of idiopathic generalized epilepsy. Patients have afebrile seizures only, with onset in adolescence (rather than in childhood) and myoclonic jerks which usually occur after awakening and are triggered by sleep deprivation and fatigue.,disease:Defects in GABRA1 are the cause of childhood absence epilepsy type 4 (ECA4) [MIM:611136]. ECA4 is a subtype of idiopathic generalized epilepsy (IGE) characterized by onset at age 6-7 years, frequent absence seizures (several per day) and bilateral, synchronous, symmetric 3-Hz spike waves on EEG. During adolescence, tonic-clonic and myoclonic seizures develop. Absence seizures may either remit or persist into adulthood.,function:GABA, the major inhibitory neurotransmitter in the vertebrate brain, mediates neuronal inhibition by binding to the GAB