UDP-β-L-Arabinofuranose (Highly Pure)

Description

UDP-β-L-Arabinofuranose
Catalog number: MDP0882
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 0.1 mg
Molecular Weight or Concentration: 536.28 g/mol
Supplied as: Triethylammonium Salt of UDP-β-L-Arabinofuranose
Applications: molecular probe for the arabinofuranose biogenesis
Storage: -20°C
Keywords: UDP-beta-L-Arabinofuranose, Uridine-5′-Diphospho- beta-L-ArabinofuranoseDP-beta-L-Araf
Grade: 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.
Indication for Use:This product is for Research Use Only. This product is NOT for human or animal use.

References:
1: Kalita M, Parker MFL, Luu JM, Stewart MN, Blecha JE, VanBrocklin HF, Evans
MJ, Flavell RR, Rosenberg OS, Ohliger MA, Wilson DM. Arabinofuranose-derived
positron-emission tomography radiotracers for detection of pathogenic
microorganisms. J Labelled Comp Radiopharm. 2020 May 15;63(5):231-239.

2: Panova MV, Podvalnyy NM, Okun EL, Abronina PI, Chizhov AO, Kononov LO.
Arabinofuranose 1,2,5-orthobenzoate as a single precursor of linear
α(1 → 5)-linked oligoarabinofuranosides. Carbohydr Res. 2018 Feb 1;456:35-44.

3: Soto MJ, Prabhakar PK, Wang HT, Backe J, Chapla D, Bartetzko M, Black IM,
Azadi P, Peña MJ, Pfrengle F, Moremen KW, Urbanowicz BR, Hahn MG. AtFUT4
and AtFUT6 Are Arabinofuranose-Specific Fucosyltransferases. Front Plant
Sci. 2021 Feb 9;12:589518.

4: Li M, Müller C, Fröhlich K, Gorka O, Zhang L, Groß O, Schilling O, Einsle O,
Jessen-Trefzer C. Detection and Characterization of a Mycobacterial
L-Arabinofuranose ABC Transporter Identified with a Rapid Lipoproteomics
Protocol. Cell Chem Biol. 2019 Jun 20;26(6):852-862.e6.

5: Mikusová K, Huang H, Yagi T, Holsters M, Vereecke D, D’Haeze W, Scherman MS,
Brennan PJ, McNeil MR, Crick DC. Decaprenylphosphoryl arabinofuranose, the donor
of the D-arabinofuranosyl residues of mycobacterial arabinan, is formed via a
two-step epimerization of decaprenylphosphoryl ribose. J Bacteriol. 2005
Dec;187(23):8020-5.

6: Kraft MB, Martinez Farias MA, Kiessling LL. Synthesis of lipid-linked
arabinofuranose donors for glycosyltransferases. J Org Chem. 2013 Mar
1;78(5):2128-33.

7: Gandolfi-Donadío L, Santos M, de Lederkremer RM, Gallo-Rodriguez C. Synthesis
of arabinofuranose branched galactofuran tetrasaccharides, constituents of
mycobacterial arabinogalactan. Org Biomol Chem. 2011 Apr 7;9(7):2085-97.

8: Podvalnyy NM, Sedinkin SL, Abronina PI, Zinin AI, Fedina KG, Torgov VI,
Kononov LO. Ring opening of acylated β-d-arabinofuranose 1,2,5-orthobenzoates
with nucleophiles allows access to novel selectively-protected arabinofuranose
building blocks. Carbohydr Res. 2011 Jan 3;346(1):7-15.

9: Zhang Q, Liu HW. Chemical synthesis of UDP-beta-L-arabinofuranose and its
turnover to UDP-beta-L-arabinopyranose by UDP-galactopyranose mutase. Bioorg Med
Chem Lett. 2001 Jan 22;11(2):145-9.
10: Rautengarten C, Ebert B, Herter T, Petzold CJ, Ishii T, Mukhopadhyay A,
Usadel B, Scheller HV. The interconversion of UDP-arabinopyranose and UDP-
arabinofuranose is indispensable for plant development in Arabidopsis. Plant
Cell. 2011 Apr;23(4):1373-90.

Products Related to UDP-β-L-Arabinofuranose : Carbohydrates