SKU: WR5177 Categories: ,

U-Blot® CHAT Rabbit mAb

Price range: $268.00 through $328.00

SKU: WR5177-100
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Product details

Background:This gene encodes an enzyme which catalyzes the biosynthesis of the neurotransmitter acetylcholine. This gene product is a characteristic feature of cholinergic neurons, and changes in these neurons may explain some of the symptoms of Alzheimer's disease. Polymorphisms in this gene have been associated with Alzheimer's disease and mild cognitive impairment. Mutations in this gene are associated with congenital myasthenic syndrome associated with episodic apnea. Multiple transcript variants encoding different isoforms have been found for this gene, and some of these variants have been shown to encode more than one isoform. [provided by RefSeq, May 2010],

Specifications

Size50μL/100μL
TargetCHAT
ReactivityHuman, Mouse, Rat
ApplicationsWB, IHC, IF, IP, ELISA
MW(Calculated)83kD
MW(Observed)83kD
Host SpeciesRabbit
IsotypeIgG,Kappa
Conjugate/ModificationUnmodified
Recommended Dilution RatioIHC 1:200-1:1000; WB 1:2000-1:10000; IF 1:200-1:1000; ELISA 1:5000-1:20000; IP 1:50-1:200; / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
PurificationRecombinant Antibody expressed in animal component-free (ACF) media, purified via Protein A affinity chromatography.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
ClonalityMonoclonal
Clone NumberRM1411R
ImmunogenThe specific immunogen used to produce this antibody is proprietary information.
SpecificityEndogenous
Gene NameCHAT
Protein NameCholine O-acetyltransferase
Other NameCHAT; / Choline O-acetyltransferase; / CHOACTase; / ChAT; / Choline acetylase
SpeciesHuman
Gene ID1103
UniprotP28329,
Species.1Mouse
Gene ID.1
Uniprot.1Q03059,
Species.2Rat
Gene ID.2
Uniprot.2P32738
Cellular Localizationnucleus,cytoplasm,cytosol,presynapse,
Tissue ExpressionBrain,Lymphocyte,Placenta,Spinal cord,
Signaling_pathwayOrganismal Systems >> Nervous system >> Cholinergic synapse
Research Areas>>Glycerophospholipid metabolism; / >>Cholinergic synapse
FunctionCatalytic activity:Acetyl-CoA + choline = CoA + O-acetylcholine.,Disease:Defects in CHAT are the cause of congenital myasthenic syndrome with episodic apnea (CMSEA) [MIM:254210]; formerly known as familial infantile myasthenia gravis 2 (FIMG2). CMSEA is an autosomal recessive congenital myasthenic syndrome. Patients have myasthenic symptoms since birth or early infancy, negative tests for anti-AChR antibodies, and abrupt episodic crises with increased weakness, bulbar paralysis, and apnea precipitated by undue exertion, fever, or excitement.,Function:Catalyzes the reversible synthesis of acetylcholine (ACh) from acetyl CoA and choline at cholinergic synapses.,online information:Choline acetyltransferase entry,similarity:Belongs to the carnitine/choline acetyltransferase family.,
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