4-Nitrophenyl α-D-mannopyranoside
<strong>4-Nitrophenyl α-D-mannopyranoside</strong>_x000D_ <strong>Catalog number:</strong> B2014435_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> 301.25 g / mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> ‚àí20¬∞C_x000D_ <strong>Keywords:</strong> 4-Nitrophenyl a-D-mannopyranoside, 4-Nitrophenyl alpha-D-mannopyranoside, pNP-alpha-D-Man, pNPalphaMan_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 -d-Mannopyranoside J Am Chem Soc. 2016 Oct 26;138(42):14012-14019._x000D_ 3: 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_ 4: Abgottspon D, Rlli 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_ 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 -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: 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._x000D_ 9: Hansen DK, Webb H, Nielsen JW, Harris P, Winther JR, Willemos M. Mutational analysis of divalent metal ion binding in the active site of class II -mannosidase from Sulfolobus solfataricus Biochemistry. 2015 Mar 24;54(11):2032-9._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/10349753">10: Sielezneff I, Mallet MN, Berthezene P, Sastre B, Dagorn JC. [Inhibition of peritoneal bacterial adhesion using oligosaccharides. An experimental model of peritonitis in rats] Chirurgie. 1999 Apr;124(2):159-64. </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: B2014435 (5 mg)
Weight
0.15
Length
2
Width
0.5
Height
0.5
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