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P-Nitrophenyl α-L-arabinopyranoside

P-Nitrophenyl α-L-arabinopyranoside is a biochemical reagent. p-Nitrophenyl α-L-arabinopyranoside can be hydrolyzed by recombinant BgaA (rBgaA, isolated from E. coli BL21 (DE3) strain harboring pEBGA29) . p-Nitrophenyl α-L-arabinopyranoside has potential application in enzyme activity detection[1][3].

Product Specifications

CAS Number

1223-07-0

UNSPSC

12352200

Hazard Statement

H315-H319-H335

Target

Biochemical Assay Reagents

Type

Biochemical Assay Reagents

Related Pathways

Others

Field of Research

Others

Assay Protocol

https://www.medchemexpress.com/p-nitrophenyl-α-l-arabinopyranoside.html

Solubility

10 mM in DMSO

Smiles

O[C@H]([C@H]([C@H](CO1)O)O)[C@@H]1OC2=CC=C([N+]([O-])=O)C=C2

Molecular Formula

C11H13NO7

Molecular Weight

271.22

Precautions

P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501

References & Citations

[1]Kosugi A, et al. Characterization of two noncellulosomal subunits, ArfA and BgaA, from Clostridium cellulovorans that cooperate with the cellulosome in plant cell wall degradation. J Bacteriol. 2002 Dec;184 (24) :6859-65.|[2]Mai V, et al. Cloning, sequencing, and characterization of the bifunctional xylosidase-arabinosidase from the anaerobic thermophile thermoanaerobacter ethanolicus. Gene. 2000 Apr 18;247 (1-2) :137-43.|[3]Shin H Y, et al. Purification and Characterization ofα-l-Arabinopyranosidase andα-l-Arabinofuranosidase from Bifidobacterium breve K-110, a Human Intestinal Anaerobic Bacterium Metabolizing Ginsenoside Rb2 and Rc[J]. Applied and environmental microbiology, 2003, 69 (12) : 7116-7123.

Shipping Conditions

Room temperature

Scientific Category

Biochemical Assay Reagents

Clinical Information

No Development Reported

Available Sizes

Frequently Asked Questions

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