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Basselin, Nguyen, Chang, Bell, Rapoport: Acute but not chronic donepezil increases muscarinic receptor-mediated signaling via arachidonic acid in unanesthetized rats. in Journal of Alzheimer's disease : JAD 2009
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Rat (Rattus) Acetylcholinesterase ELISA Kit for Sandwich ELISA - ABIN367559
Coban, Ince, Kucukkurt, Demirel, Hazman: Boron attenuates malathion-induced oxidative stress and acetylcholinesterase inhibition in rats. in Drug and chemical toxicology 2014
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Rat (Rattus) Acetylcholinesterase ELISA Kit for Sandwich ELISA - ABIN1169605
Wen, Hui, Dan, Xiao-Qiong, Jian-Bin, Chang-Qi, De-Liang, Wei-Jun, Zhi-Yuan, Xue-Gang: The effects of exercise-induced fatigue on acetylcholinesterase expression and activity at rat neuromuscular junctions. in Acta histochemica et cytochemica 2009
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Yusuf, Khan, Khan, Ahmed: Preparation, characterization, in vivo and biochemical evaluation of brain targeted Piperine solid lipid nanoparticles in an experimentally induced Alzheimer's disease model. in Journal of drug targeting 2012
hnRNP H (show HNRNPH1 ELISA Kits) binds to two specific G-runs in exon 5a of ACHE and activates the distal alternative 3 splice site (ss) between exons 5a and 5b. Furthermore, hnRNP H (show HNRNPH1 ELISA Kits) competes for binding of CstF64 to the overlapping binding sites in exon 5a, and suppresses the selection of a cryptic polyadenylation site, which additionally ensures transcription of the distal 3 ss required for the generation of AChET isoform.
these results suggest that the design and investigation of multifunctional agents containing along with the acetylcholinesterase inhibitory segment also an antioxidant moiety capable of alleviating metal (copper)-induced oxidative stress, may be of importance in the treatment of Alzheimer's disease.
Significance of AChE Genetic Variants to Risk of Toxicity from Cholinesterase (show BCHE ELISA Kits) Inhibitors (review)
miR (show MLXIP ELISA Kits)-124 could directly target the 3'-untranslated region of both signal transducer and activator of transcription 3 (STAT3 (show STAT3 ELISA Kits)) and acetylcholinesterase (AChE) mRNAs, and suppress their protein expressions.
Data suggest membranes of erythrocytes of patients with chronic obstructive pulmonary disease exhibit the following changes: increase in acetylcholinesterase; decrease in total ATPases and Na+/K+-ATPases; increase in lipid peroxidation/oxidative stress.
toxicogenetics/genetic association study in population in Turkey: Data suggest SNP in PON1 (show PON1 ELISA Kits) (192Q/R) is associated with susceptibility to organophosphate poisoning; plasma ACHE activities of exposed workers vary w/ PON1 (show PON1 ELISA Kits) genotype: 192RR>192QR>192QQ.
Data suggest cholinesterase (show BCHE ELISA Kits) inhibitors with high potency have proper conformation in active site of ACHE and interact with key residues (Trp84, Phe330 at catalytic anionic site; Trp279 at peripheral anionic site; Gly118, Gly119, Ala201 at oxyanion hole.
Phosphorylated p38 (show CRK ELISA Kits), DNMT1 (show DNMT1 ELISA Kits) and AChE were aberrantly expressed in a subset of hepatocellular carcinoma tumors.
Report acetylcholinesterase kinetics using fluorogenic probe for the investigation of free thiols.
Report reactivation kinetics of a large series of bispyridinium oximes with organophosphate-inhibited human acetylcholinesterase.
To date, AChE and BChE (show BCHE ELISA Kits) are the only proteins known that include polyproline tetramer organizing peptides in their tetrameric structure.
findings show that AChE induces a remarkable aggregation of PrP (show PRNP ELISA Kits) 106-126 with a mechanism similar to that described for amyloid beta protein
In this work, the catalytic activity of acetylcholinesterase (AChE) immobilized on these materials was investigated, using neostigmina as AChE inhibitor.
Results strongly support the role of acetylcholinesterase in triggering amyloidogenesis and the potential therapeutic relevance of peripheral site blocker compounds.
Hydrolysis of acetylthiocoline, o-nitroacetanilide and o-nitrotrifluoroacetanilide by fetal bovine serum acetylcholinesterase
iNOS (show NOS2 ELISA Kits) and AChE expression increases in spiral ganglia treated with streptomycin. Salvia miltiorrhiza injection reduces ototoxicity by reducing the levels of iNOS (show NOS2 ELISA Kits) and AChE.
Data show that 1-month of oral treatment with beta-asarone reduces AChE, Abeta42, APP (show APP ELISA Kits) and Beclin-1 (show BECN1 ELISA Kits) levels and alleviates some behavioral impairments by inhibiting the autophagy via regulating the PI3K/Akt (show AKT1 ELISA Kits)/mTOR (show FRAP1 ELISA Kits) pathway in APP (show APP ELISA Kits)/PS1 (show PSEN1 ELISA Kits) transgenic mice. The results further support the exploration of beta-asarone as a possible disease-modifying agent for the treatment of Alzheimer's disease.
Findings suggested the role of DNA methylation (show HELLS ELISA Kits) on acetylcholinesterase transcriptional regulation and provided insight in elucidating the DNA methylation (show HELLS ELISA Kits)-mediated regulatory mechanism on acetylcholinesterase expression during muscle differentiation.
Nerolidol-loaded nanospheres reverse memory impairment and to prevent increased ROS (show ROS1 ELISA Kits) and TBARS levels due to amelioration of Na(+), K(+)-ATPase (show ATP1A1 ELISA Kits) and AChE activities and to activation of the antioxidant enzymes, respectively.
the amounts of AChE activity, AChE catalytic subunit, structure subunit PRiMA (show PRIMA1 ELISA Kits) and the amount of acetylcholine, in the brain were not, significantly, altered, suggesting the role of P2Y1R in neuron could have different function as that in muscle.
In P2Y1R (-/-) mice, acetylcholinesterase expression in muscle was markedly decreased. The proline-rich membrane anchor subunit was reduced by 60 %; while the collagen tail subunit was reduced by 50 %. AChE molecular forms in the muscle were not changed.
Reduction of AChE levels in prion (show PRNP ELISA Kits)-infected heterozygous AChE knock-out mice leads to slightly but significantly prolonged incubation time.
mRNA expressions of brain specific (show CALY ELISA Kits) fatty acid protein 7 (fabp-7 (show FABP7 ELISA Kits)) and phospholipase A2 (show YWHAZ ELISA Kits) group IV (pla2g4 (show PLA2G4A ELISA Kits)) were significantly downregulated in AChE-deficient mice.
AChE is regulated in two neuronal cell lines by APP (show APP ELISA Kits) in a manner independent of the generation of sAPPalpha, sAPPbeta, and AICD.
Deficiency or inhibition of acetylcholinesterase can decrease apoptosis and protect dopaminergic neurons in the neurotoxin model of Parkinson's disease.
Attribute stress-inducible cognitive impairments to cholinergic-mediated induction of miR (show MLXIP ELISA Kits)-132 and consequently suppressed synaptic ACHE.
Findings provide evidence that brain acetylcholinesterase (AChE) is a potential target for microcystins (MCs (show MOCOS ELISA Kits)).
aryl acylamidase associated with acetylcholinesterase was higher than the esterase (show ESD ELISA Kits) activity on zebrafishembryo
Compared potency of oxime antidotes to reactivate pig brain acetylcholinesterase (AChE) after sarin exposure.
Acetylcholinesterase hydrolyzes the neurotransmitter, acetylcholine at neuromuscular junctions and brain cholinergic synapses, and thus terminates signal transmission. It is also found on the red blood cell membranes, where it constitutes the Yt blood group antigen. Acetylcholinesterase exists in multiple molecular forms which possess similar catalytic properties, but differ in their oligomeric assembly and mode of cell attachment to the cell surface. It is encoded by the single ACHE gene, and the structural diversity in the gene products arises from alternative mRNA splicing, and post-translational associations of catalytic and structural subunits. The major form of acetylcholinesterase found in brain, muscle and other tissues is the hydrophilic species, which forms disulfide-linked oligomers with collagenous, or lipid-containing structural subunits. The other, alternatively spliced form, expressed primarily in the erythroid tissues, differs at the C-terminal end, and contains a cleavable hydrophobic peptide with a GPI-anchor site. It associates with the membranes through the phosphoinositide (PI) moieties added post-translationally.
acetylcholinesterase (Yt blood group)
, acetylcholinesterase isoform E4-E6
, acetylcholine esterase
, Yt blood group
, apoptosis-related acetylcholinesterase
, glycolipid-anchored form of acetylcholinesterase