Α-mycolic Acid, Methoxy cis

<strong>α-mycolic Acid, Methoxy cis</strong>_x000D_ <strong>Catalog number:</strong> B2017927_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 1 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 1254.241_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> N/A_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: Groenewald W, Baird MS, Verschoor JA, Minnikin DE, Croft AK. Differential spontaneous folding of mycolic acids from Mycobacterium tuberculosis Chem Phys Lipids. 2014 May;180:15-22._x000D_ 2: Di Capua CB, Belardinelli JM, Carignano HA, Buchieri MV, Suarez CA, Morbidoni HR. Unveiling the Biosynthetic Pathway for Short Mycolic Acids in Nontuberculous Mycobacteria: Mycobacterium smegmatis MSMEG_4301 and Its Ortholog Mycobacterium abscessus MAB_1915 Are Essential for the Synthesis of α'-Mycolic Acids Microbiol Spectr. 2022 Aug 31;10(4):e0128822._x000D_ 3: Sakallioglu IT, Maroli AS, Leite AL, Powers R. A reversed phase ultra-high-performance liquid chromatography-data independent mass spectrometry method for the rapid identification of mycobacterial lipids J Chromatogr A. 2022 Jan 11;1662:462739._x000D_ 4: Alibaud L, Alahari A, Trivelli X, Ojha AK, Hatfull GF, Guerardel Y, Kremer L. Temperature-dependent regulation of mycolic acid cyclopropanation in saprophytic mycobacteria: role of the Mycobacterium smegmatis 1351 gene (MSMEG_1351) in CIS-cyclopropanation of alpha-mycolates J Biol Chem. 2010 Jul 9;285(28):21698-707._x000D_ 5: Beukes M, Lemmer Y, Deysel M, Al Dulayymi JR, Baird MS, Koza G, Iglesias MM, Rowles RR, Theunissen C, Grooten J, Toschi G, Roberts VV, Pilcher L, Van Wyngaardt S, Mathebula N, Balogun M, Stoltz AC, Verschoor JA. Structure-function relationships of the antigenicity of mycolic acids in tuberculosis patients Chem Phys Lipids. 2010 Nov;163(8):800-8._x000D_ 6: Muzael M, Koza G, Al Dulayymi JJ, Baird MS. The synthesis of a major alpha'-mycolic acid of Mycobacterium smegmatis Chem Phys Lipids. 2010 Sep;163(7):678-84._x000D_ 7: Sahb MM, Al Dulayymi JR, Baird MS. Glucose monomycolates based on single synthetic mycolic acids Chem Phys Lipids. 2015 Sep;190:9-14._x000D_ 8: Kaneda K, Imaizumi S, Yano I. Distribution of C22-, C24- and C26-alpha-unit-containing mycolic acid homologues in mycobacteria Microbiol Immunol. 1995;39(8):563-70._x000D_ 9: Savintseva LA, Steshin IS, Avdoshin AA, Panteleev SV, Rozhkov AV, Shirokova EA, Livshits GD, Vasyankin AV, Radchenko EV, Ignatov SK, Palyulin VA. Conformational Dynamics and Stability of Bilayers Formed by Mycolic Acids from the Mycobacterium tuberculosis Outer Membrane Molecules. 2023 Jan 31;28(3):1347._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/3781628">10: Kaneda K, Sumi Y, Kurano F, Kato Y, Yano I. Granuloma formation and hemopoiesis induced by C36-48-mycolic acid-containing glycolipids from Nocardia rubra Infect Immun. 1986 Dec;54(3):869-75. </a>_x000D_ _x000D_ <strong>Products Related to α-mycolic Acid, Methoxy cis can be found at</strong> <a href="https://moleculardepot.com/product-category/Lipids/"> Lipids</a>