X-α-L-fucopyranoside (Highly Pure)

<strong>X-α-L-fucopyranoside (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2016254_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 50 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 392.64 g/mol_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> 5-Bromo-4-chloro-3-indoxyl-α-L-fucopyranoside; X-alpha-L-Fucoside_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: Jančaříková G, Herczeg M, Fujdiarová E, Houser J, Kövér KE, Borbás A, Wimmerová M, Csávás M. Synthesis of α-l-Fucopyranoside-Presenting Glycoclusters and Investigation of Their Interaction with Photorhabdus asymbiotica Lectin (PHL) Chemistry. 2018 Mar 15;24(16):4055-4068._x000D_ 2: Gu G, Du Y, Hu H, Jin C. Synthesis of 2-chloro-4-nitrophenyl alpha-L-fucopyranoside: a substrate for alpha-L-fucosidase (AFU) Carbohydr Res. 2003 Jul 22;338(15):1603-7._x000D_ 3: Jain RK, Matta KL. Synthesis of the sodium salts of methyl 2-O-alpha-L-fucopyranosyl-alpha-L-fucopyranoside 3- and 4-sulfate Carbohydr Res. 1990 Dec 15;208:51-8._x000D_ 4: Perrella NN, Fuzita FJ, Moreti R, Verhaert PDEM, Lopes AR. First characterization of fucosidases in spiders Arch Insect Biochem Physiol. 2018 Jul;98(3):e21462._x000D_ 5: Dejter-Juszynski M, Flowers HM. Synthesis of 4-O-alpha-L-fucopyranosyl-L-fucose and methyl 4-O-beta-L-fucopyranosyl-alpha-L-fucopyranoside Carbohydr Res. 1975 May;41:308-12._x000D_ 6: Jain RK, Matta KL. Synthesis of methyl 2-O-(sodium alpha-L-fucopyranosyl 3- and 4-sulfate)-alpha-L-fucopyranoside Carbohydr Res. 1990 Dec 15;208:280-6._x000D_ 7: Grootaert H, Van Landuyt L, Hulpiau P, Callewaert N. Functional exploration of the GH29 fucosidase family Glycobiology. 2020 Aug 20;30(9):735-745._x000D_ 8: Zhang Z, Li Y, Wu M, Gao Z, Wu B, He B. Identification and Characterization of a Novel α-L-Fucosidase from Enterococcus gallinarum and Its Application for Production of 2'-Fucosyllactose Int J Mol Sci. 2023 Jul 17;24(14):11555._x000D_ 9: Benesová E, Lipovová P, Dvoráková H, Králová B. α-L-fucosidase from Paenibacillus thiaminolyticus: its hydrolytic and transglycosylation abilities Glycobiology. 2013 Sep;23(9):1052-65._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/25218034">10: Perrella NN, Cantinha RS, Nakano E, Lopes AR. Characterization of α-L-fucosidase and other digestive hydrolases from Biomphalaria glabrata Acta Trop. 2015 Jan;141(Pt A):118-27. </a>_x000D_ _x000D_ <strong>Products Related to X-α-L-fucopyranoside (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Carbohydrates/"> Carbohydrates</a>