S-Acetylthiocholine Iodide (Highly Pure)

<strong>S-Acetylthiocholine Iodide (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2016060_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 100 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 289.17_x000D_ <strong>Supplied as:</strong> Crystalline powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> 2-8°C_x000D_ <strong>Keywords:</strong> S-Acetylthiocholine Iodide AR, 99%_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Koitka M, Höchel J, Obst D, Rottmann A, Gieschen H, Borchert HH. Determination of rat serum esterase activities by an HPLC method using S-acetylthiocholine iodide and p-nitrophenyl acetate Anal Biochem. 2008 Oct 1;381(1):113-22._x000D_ 2: Chen Y, Zhang X, Luo X. Enzyme colorimetric cellulose membrane bioactivity strips based on acetylcholinesterase immobilization for inhibitors preliminary screening Colloids Surf B Biointerfaces. 2023 Mar;223:113184._x000D_ 3: Qian S, Lin H. Colorimetric sensor array for detection and identification of organophosphorus and carbamate pesticides Anal Chem. 2015;87(10):5395-400._x000D_ 4: Li H, Guo Y, Xiao L, Chen B. Selective and sensitive detection of acetylcholinesterase activity using denatured protein-protected gold nanoclusters as a label-free probe Analyst. 2014 Jan 7;139(1):285-9._x000D_ 5: Anlezark GM, Melton RG, Sherwood RF, Wilson WR, Denny WA, Palmer BD, Knox RJ, Friedlos F, Williams A. Bioactivation of dinitrobenzamide mustards by an E. coli B nitroreductase Biochem Pharmacol. 1995 Aug 25;50(5):609-18._x000D_ 6: Hamers T, Molin KR, Koeman JH, Murk AJ. A small-volume bioassay for quantification of the esterase inhibiting potency of mixtures of organophosphate and carbamate insecticides in rainwater: development and optimization Toxicol Sci. 2000 Nov;58(1):60-7._x000D_ 7: Knox RJ, Friedlos F, Marchbank T, Roberts JJ. Bioactivation of CB 1954: reaction of the active 4-hydroxylamino derivative with thioesters to form the ultimate DNA-DNA interstrand crosslinking species Biochem Pharmacol. 1991 Oct 9;42(9):1691-7._x000D_ 8: Nitecka L, Narkiewicz O. Localization of acetylcholinesterase activity in the amygdaloid body of man Acta Neurobiol Exp (Wars). 1976;36(3):333-51._x000D_ 9: Bucur MP, Bucur B, Radu GL. Critical evaluation of acetylthiocholine iodide and acetylthiocholine chloride as substrates for amperometric biosensors based on acetylcholinesterase Sensors (Basel). 2013 Jan 25;13(2):1603-13._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/30877329">10: Estévez J, Rodrigues de Souza F, Romo M, Mangas I, Costa Franca TC, Vilanova E. Interactions of human butyrylcholinesterase with phenylvalerate and acetylthiocholine as substrates and inhibitors: kinetic and molecular modeling approaches Arch Toxicol. 2019 May;93(5):1281-1296. </a>_x000D_ _x000D_ <strong>Products Related to S-Acetylthiocholine Iodide (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>