1-Stearoyl-sn-glycero-3-phosphocholine

<strong>1-Stearoyl-sn-glycero-3-phosphocholine</strong>_x000D_ <strong>Catalog number:</strong> B2017464_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 5 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 523.68_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> −20°C_x000D_ <strong>Keywords:</strong> L-α-Lysophosphatidylcholine, stearoyl, Lysolecithin, stearoyl_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: Jung JH, Jeong SJ, Kim JH, Jung SK, Jung DB, Lee D, Sohn EJ, Yun M, Lee HJ, Lee HJ, Kim SH. Inactivation of HDAC3 and STAT3 is critically involved in 1-stearoyl-sn-glycero-3-phosphocholine-induced apoptosis in chronic myelogenous leukemia K562 cells Cell Biochem Biophys. 2013;67(3):1379-89._x000D_ 2: Broadhurst CL, Schmidt WF, Nguyen JK, Qin J, Chao K, Kim MS. Continuous gradient temperature Raman spectroscopy from -100 to 40°C yields new molecular models of arachidonic acid and 2-Arachidonoyl-1-stearoyl-sn-glycero-3-phosphocholine Prostaglandins Leukot Essent Fatty Acids. 2017 Dec;127:6-15._x000D_ 3: Tam J, Ahmad IAH, Blasko A. A four parameter optimization and troubleshooting of a RPLC - charged aerosol detection stability indicating method for determination of S-lysophosphatidylcholines in a phospholipid formulation J Pharm Biomed Anal. 2018 Jun 5;155:288-297._x000D_ 4: Hanel AM, Schüttel S, Gelb MH. Processive interfacial catalysis by mammalian 85-kilodalton phospholipase A2 enzymes on product-containing vesicles: application to the determination of substrate preferences Biochemistry. 1993 Jun 15;32(23):5949-58._x000D_ 5: Kusano M, Kawabata S, Tamura Y, Mizoguchi D, Murouchi M, Kawasaki H, Arakawa R, Tanaka K. Laser Desorption/Ionization Mass Spectrometry (LDI-MS) of Lipids with Iron Oxide Nanoparticle-Coated Targets Mass Spectrom (Tokyo). 2014;3(1):A0026._x000D_ 6: Davis PJ, Fleming BD, Coolbear KP, Keough KM. Gel to liquid-crystalline transition temperatures of water dispersions of two pairs of positional isomers of unsaturated mixed-acid phosphatidylcholines Biochemistry. 1981 Jun 9;20(12):3633-6._x000D_ 7: Panasenko OM, Osipov AN, Schiller J, Arnhold J. Interaction of exogenous hypochlorite or hypochlorite produced by myeloperoxidase + H2O2 + Cl- system with unsaturated phosphatidylcholines Biochemistry (Mosc). 2002 Aug;67(8):889-900._x000D_ 8: Flasiński M, Broniatowski M, Majewski J, Dynarowicz-Łatka P. X-ray grazing incidence diffraction and Langmuir monolayer studies of the interaction of beta-cyclodextrin with model lipid membranes J Colloid Interface Sci. 2010 Aug 15;348(2):511-21._x000D_ 9: Shim J, Kim MJ, Kim HK, Kim DH, Oh SG, Ko SY, Jang HG, Kim JW. Morphological effect of lipid carriers on permeation of lidocaine hydrochloride through lipid membranes Int J Pharm. 2010 Mar 30;388(1-2):251-6._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/22952663">10: Soler-Cantero A, Jové M, Cacabelos D, Boada J, Naudí A, Romero MP, Cassanyé A, Serrano JC, Arola L, Valls J, Bellmunt MJ, Prat J, Pamplona R, Portero-Otin M, Motilva MJ. Plant-derived phenolics inhibit the accrual of structurally characterised protein and lipid oxidative modifications PLoS One. 2012;7(8):e43308. </a>_x000D_ _x000D_ <strong>Products Related to 1-Stearoyl-sn-glycero-3-phosphocholine can be found at</strong> <a href="https://moleculardepot.com/product-category/Lipids/"> Lipids</a>