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4-Nitrophenyl α-L-arabinofuranoside

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For Research Use Only | Not For Clinical Use
CATAP6892586
CAS6892-58-6
Structure
MDL NumberMFCD00057269
Molecular Weight271.22
InChI KeyDUYYBTBDYZXISX-UKKRHICBSA-N
REAXYS Number1688357
Description≥98% (TLC)
Assay≥98% (TLC)
Size10MG, 25MG, 100MG
Storage Conditions−20°C
1

A GH51 α-L-arabinofuranosidase From Talaromyces Leycettanus Strain JCM12802 That Selectively Drives Synergistic Lignocellulose Hydrolysis

Tao Tu, Xiaoli Li, Kun Meng, Yingguo Bai, Yuan Wang, Zhenxing Wang, Bin Yao, Huiying Luo

Microb Cell Fact. 2019 Aug 19;18(1):138.

PMID: 31426823

1

A Novel Bifunctional GH51 exo-α-l-arabinofuranosidase/endo-xylanase From Alicyclobacillus Sp. A4 With Significant Biomass-Degrading Capacity

Wenxia Yang, Yingguo Bai, Peilong Yang, Huiying Luo, Huoqing Huang, Kun Meng, Pengjun Shi, Yaru Wang, Bin Yao

Biotechnol Biofuels. 2015 Nov 30;8:197.

PMID: 26628911

1

Elucidation of the Molecular Basis for Arabinoxylan-Debranching Activity of a Thermostable Family GH62 α-l-arabinofuranosidase From Streptomyces Thermoviolaceus

Weijun Wang, Galina Mai-Gisondi, Peter J Stogios, Amrit Kaur, Xiaohui Xu, Hong Cui, Ossi Turunen, Alexei Savchenko, Emma R Master

Appl Environ Microbiol. 2014 Sep;80(17):5317-29.

PMID: 24951792

1

Thermodynamics of the Hydrolysis Reactions of 1-naphthyl Acetate, 4-nitrophenyl Acetate, and 4-nitrophenyl α-L-arabinofuranoside

Stephen R Decker, Robert N Goldberg, Brian E Lang, William Michener

J Phys Chem B. 2010 Dec 16;114(49):16060-7.

PMID: 20361764

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