ACHA2 rabbit pAb

ACHA2 rabbit pAb

AO-06-ES18494-50

ACHA2 rabbit pAb 50μL

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€299.00
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Antibody Product Overview

ELK.NoES18494
Product nameACHA2 rabbit pAb
ReactivityHuman; Mouse;Rat
ApplicationsWB
Other name
Size50μL
Unit price ($)148
Human gene ID1135
Human Swiss-ProtQ15822
SourceRabbit
IsotypeIgG
TargetACHA2
Fields>>Neuroactive ligand-receptor interaction
Gene nameCHRNA2
Protein nameACHA2
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID110902
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ91X60
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID170945
Rat gene linkView Rat Gene
Rat Swiss-ProtP12389
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from human ACHA2 AA range: 219-269
SpecificityThis antibody detects endogenous levels of ACHA2 at Human/Mouse/Rat
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)58kD
Observed band (KD)
BackgroundNicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels formed by a pentameric arrangement of alpha and beta subunits to create distinct muscle and neuronal receptors. Neuronal receptors are found throughout the peripheral and central nervous system where they are involved in fast synaptic transmission. This gene encodes an alpha subunit that is widely expressed in the brain. The proposed structure for nAChR subunits is a conserved N-terminal extracellular domain followed by three conserved transmembrane domains, a variable cytoplasmic loop, a fourth conserved transmembrane domain, and a short C-terminal extracellular region. Mutations in this gene cause autosomal dominant nocturnal frontal lobe epilepsy type 4. Single nucleotide polymorphisms (SNPs) in this gene have been associated with nicotine dependence. [provided by RefSeq, Nov 2009],
Functiondisease:Defects in CHRNA2 are the cause of nocturnal frontal lobe epilepsy type 4 (ENFL4) [MIM:610353]. ENFL4 is an autosomal dominant epilepsy characterized by nocturnal seizures associated with fear sensation, tongue movements, and nocturnal wandering, closely resembling nightmares and sleep walking.,function:After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane.,similarity:Belongs to the ligand-gated ionic channel (TC 1.A.9) family.,subunit:Neuronal AChR seems to be composed of two different types of subunits: alpha and non-alpha (beta). Alpha-2 subunit can be combined to beta-2 or beta-4 to give rise to functional receptors.,
Subcellular locationCell junction, synapse, postsynaptic cell membrane; Multi-pass membrane protein. Cell membrane; Multi-pass membrane protein.
Expression

Additional Images

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Western blot analysis of lysates from SW480 cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES18494-50
: 10 Items
Hurry! only 10 items left in stock.

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