4-Nitrophenyl-α-L-arabinofuranoside
$695.00
Catalog Number: B2014502 (25 mg)
4-Nitrophenyl-α-L-arabinofuranoside is a high quality 4-Nitrophenyl-α-L-arabinofuranoside, a colorimetric substrate for the measurement of α-L-arabinofuranosidase activity. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.
Live enquiry about this product via Text/SMS: 1-858-900-3210.
In stock
Description
4-Nitrophenyl-α-L-arabinofuranoside
Catalog number: B2014502
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 25 mg
Molecular Weight or Concentration: 271.2
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: -20oC
Keywords:
4-Nitrophenyl-α-L-arabinofuranoside
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.
References:
1: Decker SR, Goldberg RN, Lang BE, Michener W. Thermodynamics of the hydrolysis reactions of 1-naphthyl acetate, 4-nitrophenyl acetate, and 4-nitrophenyl α-L-arabinofuranoside J Phys Chem B. 2010 Dec 16;114(49):16060-7.
2: Mastihubová M, Szemesová J, Biely P. The acetates of p-nitrophenyl alpha-L-arabinofuranoside–regioselective preparation by action of lipases Bioorg Med Chem. 2006 Mar 15;14(6):1805-10.
3: Biely P, Mastihubová M, Tenkanen M, Eyzaguirre J, Li XL, Vršanská M. Action of xylan deacetylating enzymes on monoacetyl derivatives of 4-nitrophenyl glycosides of β-D-xylopyranose and α-L-arabinofuranose J Biotechnol. 2011 Jan 10;151(1):137-42.
4: Renner MJ, Breznak JA. Purification and properties of ArfI, an alpha-L-arabinofuranosidase from Cytophaga xylanolytica Appl Environ Microbiol. 1998 Jan;64(1):43-52.
5: Herrmann MC, Vrsanska M, Jurickova M, Hirsch J, Biely P, Kubicek CP. The beta-D-xylosidase of Trichoderma reesei is a multifunctional beta-D-xylan xylohydrolase Biochem J. 1997 Jan 15;321 ( Pt 2)(Pt 2):375-81.
6: Diener A. Visualizing and quantifying Fusarium oxysporum in the plant host Mol Plant Microbe Interact. 2012 Dec;25(12):1531-41.
7: Akkaya A, Ensari Y, Ozseker EE, Batur OO, Buyuran G, Evran S. Recombinant Production and Biochemical Characterization of Thermostable Arabinofuranosidase from Acidothermophilic Alicyclobacillus Acidocaldarius Protein J. 2023 Aug;42(4):437-450.
8: Tu T, Li X, Meng K, Bai Y, Wang Y, Wang Z, Yao B, Luo H. A GH51 α-L-arabinofuranosidase from Talaromyces leycettanus strain JCM12802 that selectively drives synergistic lignocellulose hydrolysis Microb Cell Fact. 2019 Aug 19;18(1):138.
9: Lee CC, Braker JD, Grigorescu AA, Wagschal K, Jordan DB. Divalent metal activation of a GH43 β-xylosidase Enzyme Microb Technol. 2013 Feb 5;52(2):84-90.
10: Shi P, Chen X, Meng K, Huang H, Bai Y, Luo H, Yang P, Yao B. Distinct actions by Paenibacillus sp. strain E18 α-L-arabinofuranosidases and xylanase in xylan degradation Appl Environ Microbiol. 2013 Mar;79(6):1990-5.
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4-Nitrophenyl-α-L-arabinofuranoside can be found at Carbohydrates
Additional information
Weight | 48 oz |
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Dimensions | 8 × 8 × 8 in |
How to Order
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