4-Nitrophenyl α-D-Mannopyranoside
<strong>4-Nitrophenyl α-D-Mannopyranoside</strong>_x000D_ <strong>Catalog number:</strong> B2012272_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> 301.3 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20C_x000D_ <strong>Keywords:</strong> 4-Nitrophenyl α-D-Mannopyranoside_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MŒ©-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Kanellopoulos PN, Pavlou K, Perrakis A, Agianian B, Vorgias CE, Mavrommatis C, Soufi M, Tucker PA, Hamodrakas SJ. The crystal structure of the complexes of concanavalin A with 4'-nitrophenyl-alpha-D-mannopyranoside and 4'-nitrophenyl-alpha-D-glucopyranoside J Struct Biol. 1996 May-Jun;116(3):345-55._x000D_ 2: Speciale G, Farren-Dai M, Shidmoossavee FS, Williams SJ, Bennet AJ. C2-Oxyanion Neighboring Group Participation: Transition State Structure for the Hydroxide-Promoted Hydrolysis of 4-Nitrophenyl α-d-Mannopyranoside J Am Chem Soc. 2016 Oct 26;138(42):14012-14019._x000D_ 3: Abgottspon D, R√∂lli G, Hosch L, Steinhuber A, Jiang X, Schwardt O, Cutting B, Smiesko M, Jenal U, Ernst B, Trampuz A. Development of an aggregation assay to screen FimH antagonists J Microbiol Methods. 2010 Sep;82(3):249-55._x000D_ 4: Hamodrakas SJ, Alexandraki E, Troganis A, Stassinopoulou CI. Models of binding of 4'-nitrophenyl alpha-D-mannopyranoside to the lectin concanavalin A Int J Biol Macromol. 1989 Feb;11(1):17-22._x000D_ 5: Rajesh T, Jeon JM, Song E, Park HM, Seo HM, Kim HJ, Yi DH, Kim YH, Choi KY, Kim YG, Park HY, Lee YK, Yang YH. Putative role of a Streptomyces coelicolor-derived α-mannosidase in deglycosylation and antibiotic production Appl Biochem Biotechnol. 2014 Feb;172(3):1639-51._x000D_ 6: Jelinek-Kelly S, Akiyama T, Saunier B, Tkacz JS, Herscovics A. Characterization of a specific alpha-mannosidase involved in oligosaccharide processing in Saccharomyces cerevisiae J Biol Chem. 1985 Feb 25;260(4):2253-7._x000D_ 7: Madiyalakan R, Piskorz CF, Piver MS, Matta KL. Serum beta-(1----4)-galactosyltransferase activity with synthetic low molecular weight acceptor in human ovarian cancer Eur J Cancer Clin Oncol. 1987 Jul;23(7):901-6._x000D_ 8: Howard S, Braun C, McCarter J, Moremen KW, Liao YF, Withers SG. Human lysosomal and jack bean alpha-mannosidases are retaining glycosidases Biochem Biophys Res Commun. 1997 Sep 29;238(3):896-8._x000D_ 9: Hansen DK, Webb H, Nielsen JW, Harris P, Winther JR, Willemo√´s M. Mutational analysis of divalent metal ion binding in the active site of class II α-mannosidase from Sulfolobus solfataricus Biochemistry. 2015 Mar 24;54(11):2032-9._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/3997852">10: Ohyama Y, Kasai K, Nomoto H, Inoue Y. Frontal affinity chromatography of ovalbumin glycoasparagines on a concanavalin A-sepharose column. A quantitative study of the binding specificity of the lectin J Biol Chem. 1985 Jun 10;260(11):6882-7.</a>_x000D_ _x000D_ <strong>Products Related to 4-Nitrophenyl α-D-Mannopyranoside can be found at</strong> <a href="https://moleculardepot.com/product-category/Substrates/"> Substrates</a>
Product Specifications
Short Description
Catalog Number: B2012272 (100 mg)
Weight
0.15
Length
2
Width
0.5
Height
0.5
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