Linoleic Acid Methyl Ester Mix
<strong>Linoleic Acid Methyl Ester Mix</strong>_x000D_ <strong>Catalog number:</strong> B2018213_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 1 mL_x000D_ <strong>Molecular Weight or Concentration:</strong> N/A_x000D_ <strong>Supplied as:</strong> Solution_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20℃_x000D_ <strong>Keywords:</strong> N/A_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Maekawa M, Kawai K, Takahashi Y, Nakamura H, Watanabe T, Sawa R, Hachisuka K, Kasai H. Identification of 4-oxo-2-hexenal and other direct mutagens formed in model lipid peroxidation reactions as dGuo adducts Chem Res Toxicol. 2006 Jan;19(1):130-8._x000D_ 2: Thaiyasuit P, Pianthong K, Worapun I. Acid esterification-alkaline transesterification process for methyl ester production from crude rubber seed oil J Oleo Sci. 2012;61(2):81-8._x000D_ 3: Pajunen TI, Johansson MP, Hase T, Hopia A. Autoxidation of conjugated linoleic acid methyl ester in the presence of alpha-tocopherol: the hydroperoxide pathway Lipids. 2008 Jul;43(7):599-610._x000D_ 4: Fagali N, Catalá A. Antioxidant activity of conjugated linoleic acid isomers, linoleic acid and its methyl ester determined by photoemission and DPPH techniques Biophys Chem. 2008 Sep;137(1):56-62._x000D_ 5: Slim R, Hammock BD, Toborek M, Robertson LW, Newman JW, Morisseau CH, Watkins BA, Saraswathi V, Hennig B. The role of methyl-linoleic acid epoxide and diol metabolites in the amplified toxicity of linoleic acid and polychlorinated biphenyls to vascular endothelial cells Toxicol Appl Pharmacol. 2001 Mar 15;171(3):184-93._x000D_ 6: Catala A, Brenner RR. Relative incorporation of linoleic and arachidonic acid in phospholipids and triglycerides of different rat tissues Lipids. 1967 Mar;2(2):114-21._x000D_ 7: Aboshi T, Shimizu N, Nakajima Y, Honda Y, Kuwahara Y, Amano H, Mori N. Biosynthesis of linoleic acid in Tyrophagus mites (Acarina: Acaridae) Insect Biochem Mol Biol. 2013 Nov;43(11):991-6._x000D_ 8: Fan H, Smuts J, Bai L, Walsh P, Armstrong DW, Schug KA. Gas chromatography-vacuum ultraviolet spectroscopy for analysis of fatty acid methyl esters Food Chem. 2016 Mar 1;194:265-71._x000D_ 9: Schwinn J, Sprinz H, Drössler K, Leistner S, Brede O. Thiyl radical-induced cis/trans-isomerization of methyl linoleate in methanol and of linoleic acid residues in liposomes Int J Radiat Biol. 1998 Sep;74(3):359-65._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/403382">10: Matthew JA, Chan HW, Galliard T. A simple method for the preparation of pure 9-D-hydroperoxide of linoleic acid and methyl linoleate based on the positional specificity of lipoxygenase in tomato fruit Lipids. 1977 Mar;12(3):324-6. </a>_x000D_ _x000D_ <strong>Products Related to Linoleic Acid Methyl Ester Mix can be found at</strong> <a href="https://moleculardepot.com/product-category/Lipids/"> Lipids</a>
Product Specifications
Short Description
Catalog Number: B2018213 (1 mL)
Weight
0.15
Length
2
Width
0.5
Height
0.5
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