Q25120
QAE Sephadex® A-25 氯化物形式
别名:
二乙基（2-羟丙基）氨基乙基葡聚糖凝胶®
bead size
40-125 μm (dry)
pore size
~30,000 Da exclusion limit
operating pH
2-10
capacity
2.6-3.4 meq/g ion exchange capacity
compatibility
mode of use strong anion exchange chromatography
Quality Level
General description
Q25120-100G 的更新产品编号为 GE17-0190-01
Application
QAE Sephadex® 用于蛋白质色谱、离子交换色谱、阴离子交换介质、树脂和分离介质。QAE Sephadex® 已用于开发检测水样中的铜、啤酒中的白藜芦醇以及药品和尿液样品中消炎痛的方法。
Legal Information
Sephadex is a registered trademark of Cytiva
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
A B Cantor et al.
The Journal of biological chemistry, 267(32), 23349-23356 (1992-11-15)
Cathepsin D is a bilobed lysosomal aspartyl protease that contains one Asn-linked oligosaccharide/lobe. Each lobe also contains protein determinants that serve as recognition domains for binding of UDP-GlcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase, the first enzyme in the biosynthesis of the mannose 6-phosphate
Purification and Partial Characterization of Host-Specific Toxins Produced by <I>Periconia circinata</I>.
Wolpert, T.J., and Dunkle, L.D.
Phytopathology, 70, 872-876 (1980)
3-deoxy-d-manno-2-octulosonic acid (KDO) is a component of rhamnogalacturonan II, a pectic polysaccharide in the primary cell walls of plants.
York, W.S., et al.
Carbohydrate Research, 138(1), 109-126 (1985)
A Varki et al.
Archives of biochemistry and biophysics, 222(1), 145-149 (1983-04-01)
An enzyme that is capable of removing the outer N-acetylglucosamine residues from phosphodiesters present on the high-mannose-type oligosaccharides of newly synthesized lysosomal enzymes has been described. This enzyme has been called an alpha-N-acetylglucosaminylphosphodiesterase, based upon its substrate specificity and on
Lucía Molina-García et al.
Journal of AOAC International, 93(5), 1443-1449 (2010-12-15)
A selective and sensitive method based on coupling of sequential injection analysis (SIA) and optosensing was developed and applied to the determination of indomethacin in pharmaceutical and urinary samples. After alkaline hydrolysis, the fluorescent product generated from indomethacin is inserted
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