推荐产品
product name
4-硝基苯基 α-L-阿拉伯呋喃糖苷, ≥98% (TLC)
化驗
≥98% (TLC)
形狀
powder
溶解度
methanol: 50 mg/mL
儲存溫度
−20°C
SMILES 字串
OC[C@@H]1O[C@@H](Oc2ccc(cc2)[N+]([O-])=O)[C@H](O)[C@H]1O
InChI
1S/C11H13NO7/c13-5-8-9(14)10(15)11(19-8)18-7-3-1-6(2-4-7)12(16)17/h1-4,8-11,13-15H,5H2/t8-,9-,10+,11+/m0/s1
InChI 密鑰
DUYYBTBDYZXISX-UKKRHICBSA-N
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應用
4-硝基苯基-α-L-阿拉伯呋喃糖苷已用于:
- 在酶促测定中作为α-阿拉伯呋喃糖苷酶的底物,测定酒球菌(Oenococcus oeni )菌株中的糖苷酶活性
- 测定α-阿拉伯呋喃糖苷酶的酶活性
- 用作对硝基苯酚连接底物,测定其在黑曲霉(Aspergillus niger)NW249培养滤液中的活性
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
其他客户在看
Biotechnology journal, 9(10), 1329-1338 (2014-08-15)
Plant-degrading enzymes can be produced by fungi on abundantly available low-cost plant biomass. However, enzymes sets after growth on complex substrates need to be better understood, especially with emphasis on differences between fungal species and the influence of inhibitory compounds
Planta, 241(5), 1159-1172 (2015-01-23)
Specific α- l -arabinofuranosidases are involved in the realisation of elongation growth process in cells with type II cell walls. Elongation growth in a plant cell is largely based on modification of the cell wall. In type II cell walls
Journal of bacteriology, 190(12), 4272-4280 (2008-04-15)
The extracellular depolymerization of arabinopolysaccharides by microorganisms is accomplished by arabinanases, xylanases, and galactanases. Here, we characterize a novel endo-alpha-1,5-l-arabinanase (EC 3.2.1.99) from Bacillus subtilis, encoded by the yxiA gene (herein renamed abn2) that contributes to arabinan degradation. Functional studies
Preparation of arabinoxylobiose from rye xylan using family 10 Aspergillus aculeatus endo-1, 4-beta-D-xylanase
Carbohydrate Polymers null
Applied and environmental microbiology, 64(1), 43-52 (1998-01-22)
An alpha-L-arabinofuranosidase (alpha-L-arabinofuranoside arabinofuranohydrolase [EC 3.2.1.55]; referred to below as ArfI) from Cytophaga xylanolytica XM3 was purified 85-fold by anion-exchange and hydrophobic interaction column chromatography. The native enzyme had a pI of 6.1 and an apparent molecular mass of 160
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