GABAA Rα1 rabbit pAb

GABAA Rα1 rabbit pAb

AO-06-ES4299-100

GABAA Rα1 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES4299
Product nameGABAA Rα1 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC;IF;ELISA
Other nameGABRA1; Gamma-aminobutyric acid receptor subunit alpha-1; GABA(A) receptor subunit alpha-1
Size100μL
Unit price ($)248
Human gene ID2554
Human Swiss-ProtP14867
SourceRabbit
IsotypeIgG
TargetGABAA Rα1
Fields>>Neuroactive ligand-receptor interaction;>>Retrograde endocannabinoid signaling;>>GABAergic synapse;>>Taste transduction;>>Morphine addiction;>>Nicotine addiction
Gene nameGABRA1
Protein nameGamma-aminobutyric acid receptor subunit alpha-1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID14394
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP62812
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID29705
Rat gene linkView Rat Gene
Rat Swiss-ProtP62813
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from the Internal region of human GABRA1. AA range:61-110
SpecificityGABAA Rα1 Polyclonal Antibody detects endogenous levels of GABAA Rα1 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. IHC-p: 1:100-1:300. ELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)50kD
BackgroundThis 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],
Functiondisease: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
Subcellular locationCell junction, synapse, postsynaptic cell membrane ; Multi-pass membrane protein . Cell membrane ; Multi-pass membrane protein . Cytoplasmic vesicle membrane .
ExpressionBrain,Cerebellum,Cerebrum,

Additional Images

Image 1
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Western Blot analysis of NIH-3T3, KB cells using GABAA Rα1 Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Immunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100
Image 3
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Immunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100
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Immunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100
: AO-06-ES4299-100
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Hurry! only 10 items left in stock.

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