AChRα1 rabbit pAb

AChRα1 rabbit pAb

AO-06-ES4285-50

AChRα1 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES4285
Product nameAChRα1 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IF;ELISA
Other nameCHRNA1; ACHRA; CHNRA; Acetylcholine receptor subunit alpha
Size50μL
Unit price ($)148
Human gene ID1134
Human Swiss-ProtP02708
SourceRabbit
IsotypeIgG
TargetAChRα1
Fields>>Neuroactive ligand-receptor interaction
Gene nameCHRNA1
Protein nameAcetylcholine receptor subunit alpha
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID11435
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP04756
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID79557
Rat gene linkView Rat Gene
Rat Swiss-ProtP25108
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from the Internal region of human CHRNA1. AA range:171-220
SpecificityAChRα1 Polyclonal Antibody detects endogenous levels of AChRα1 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/5000. IF 1:100-300 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)55kD
BackgroundThe muscle acetylcholine receptor consiststs of 5 subunits of 4 different types: 2 alpha subunits and 1 each of the beta, gamma, and delta subunits. This gene encodes an alpha subunit that plays a role in acetlycholine binding/channel gating. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Nov 2012],
Functiondisease:Defects in CHRNA1 are a cause of congenital myasthenic syndrome fast-channel type (FCCMS) [MIM:608930]. FCCMS is a congenital myasthenic syndrome characterized by kinetic abnormalities of the AChR. In most cases, FCCMS is due to mutations that decrease activity of the AChR by slowing the rate of opening of the receptor channel, speeding the rate of closure of the channel, or decreasing the number of openings of the channel during ACh occupancy. The result is failure to achieve threshold depolarization of the endplate and consequent failure to fire an action potential.,disease:Defects in CHRNA1 are a cause of congenital myasthenic syndrome slow-channel type (SCCMS) [MIM:601462]. SCCMS is the most common congenital myasthenic syndrome. Congenital myasthenic syndromes are characterized by muscle weakness affecting the axial and limb muscles (with hypotonia in early-onset forms), the
Subcellular locationCell junction, synapse, postsynaptic cell membrane ; Multi-pass membrane protein . Cell membrane ; Multi-pass membrane protein .
ExpressionIsoform 1 is only expressed in skeletal muscle. Isoform 2 is constitutively expressed in skeletal muscle, brain, heart, kidney, liver, lung and thymus.

Additional Images

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Immunofluorescence analysis of A549. 1,primary Antibody was diluted at 1:200(4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 488 Secondary antibody was diluted at 1:1000(room temperature, 50min).3, Picture B: DAPI(blue) 10min.
Image 2
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Western Blot analysis of NIH-3T3 cells using AChRα1 Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
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: AO-06-ES4285-50
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Hurry! only 10 items left in stock.

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