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Human GABRA3 Stable Cell Line-HEK293

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Cat.No.
CSC-RI0006
Background
GABA is the major inhibitory neurotransmitter in the CNS, binding to fast-acting ionotropic GABAAreceptors to cause inward flux of Cl- resulting in membrane hyperpolarization and thus reducing membrane excitability. Excessive stimulation of these receptors can lead to sedation and ataxia whereas attenuation leads to arousal, insomnia and anxiety. Since modulation of these receptors has such profound physiological effects they have become important drug targets for the treatment of many conditions e.g. anxiety, epilepsy, sleep disorders and for anesthesia. GABAA receptors are pentameric structures typically consisting of alpha, beta and gamma2 subunits in a stoichiometry of 2:2:1. The specific subunit composition is especially important since various combinations mediate different effects. For example, alpha1-containing receptors, accounting for 60% of all GABAA receptors, mediate the sedative/hypnotic effects of benzodiazepines (BZPs) whereas the anxiolytic effects of these drugs are mediated by receptors containing alpha2 and alpha3 subunits. Hence, developing selective allosteric modulators for these latter subunits should ultimately lead to anxiolytic drugs devoid of unwanted sedative effects.
Growth Properties
Adherent
Morphology
Epithelial
Host Cell
HEK293
Ship
Dry ice
Gene Information
Official Symbol
GABRA3
Synonyms
GABRA3; gamma-aminobutyric acid (GABA) A receptor, alpha 3; gamma-aminobutyric acid receptor subunit alpha-3; GABA(A) receptor; alpha 3; GABA(A) receptor, alpha 3; GABA(A) receptor subunit alpha-3; gamma-animobutyric acid (GABA) A receptor, alpha 3; MGC33793;
Gene ID
MIM
UniProt ID
P34903
Chromosome Location
Xq28
Pathway
GABA A receptor activation, organism-specific biosystem; GABA receptor activation, organism-specific biosystem; GABAergic synapse, organism-specific biosystem; GABAergic synapse, conserved biosystem; Ion channel transport, organism-specific biosystem; Ligand-gated ion channel transport, organism-specific biosystem; Morphine addiction, organism-specific biosystem;
Function
GABA-A receptor activity; benzodiazepine receptor activity; chloride channel activity; extracellular ligand-gated ion channel activity; ion channel activity; receptor activity;

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