Merck

55505-U

Supelco

Discovery® Glycan SPE Tube

5 g, volume 60 mL, pk of 16

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NACRES:
NB.21

物料

PE frit
polypropylene

质量水平

组成

, 5 g

包装

pk of 16

技术

solid phase extraction (SPE): suitable

体积

60 mL

杂质

<5% Water content

基质

polyamide resin base material

基质活性基团

amide, poly- phase

粒径

50-160 μm

pH值范围

4.5-7.5(surface pH)

堆积密度

0.2‑0.3 g/mL

分离技术

reversed phase

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此商品
55467-U55482-U55487-U
Supelco

55505-U

Discovery® Glycan SPE Tube

Supelco

55467-U

Discovery® Glycan SPE Tube

Supelco

55482-U

Discovery® Glycan SPE Tube

Supelco

55487-U

Discovery® Glycan SPE Tube

particle size

50-160 μm

particle size

50-160 μm

particle size

50-160 μm

particle size

50-160 μm

matrix

polyamide resin base material

matrix

polyamide resin base material

matrix

polyamide resin base material

matrix

polyamide resin base material

separation technique

reversed phase

separation technique

reversed phase

separation technique

reversed phase

separation technique

reversed phase

volume

60 mL

volume

3 mL

volume

6 mL

volume

12 mL

material

PE frit, polypropylene

material

PE frit, polypropylene

material

PE frit, polypropylene

material

PE frit, polypropylene

一般描述

Retention Mechanism: Reversed-phase
Sample Matrix Compatibility: Aqueous or methanolic solutions

  • Polyamide Resin: Particle Size: 50-160 μm, Surf pH: 4.5-7.5, Density: 0.2-0.3 cm3/g, Water Content: < 5 %
  • Useful for extracting gylcans from aqueous solutions.
  • Used to adsorb polar compounds (-OH groups, esp. phenolic compounds) from aqueous or methanolic solutions under the reversed-phase mechanism through strong hydrogen bonding between compound hydroxyl groups and amide groups of the resin
  • Also may be used for the extraction of tannins, chlorophyll, humic acid, pharmacologically active terpenoids, flavanoids, gallic acid, catechol A, protocatechuic acid, phloroglucinol, aromatic carboxylic acids, and nitroaromatic compounds
  • Irreversibly retains quinones.

法律信息

Discovery is a registered trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Hsin-Yuan Chen et al.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 49(5), 1970-1986 (2018-09-21)
Uterine leiomyomas (ULs) are benign uterine tumors, and the most notable pathophysiologic feature of ULs is excessive accumulation of extracellular matrix (ECM). Fucoidan is a polysaccharide extracted from brown seaweeds that has a wide range of pharmacological properties, including anti-fibrotic
Wei Liu et al.
Glycobiology, 28(6), 363-373 (2018-03-22)
O-linked N-acetylglucosamine (O-GlcNAcylation) is an important post-translational modification on serine or threonine of proteins, mainly observed in nucleus or cytoplasm. O-GlcNAcylation regulates many cell processes, including transcription, cell cycle, neural development and nascent polypeptide chains stabilization. However, the facile identification
Qi Gu et al.
Methods in molecular biology (Clifton, N.J.), 1758, 129-138 (2018-04-22)
Bioprinting provides an opportunity to produce three-dimensional (3D) tissues for biomedical research and translational drug discovery, toxicology, and tissue replacement. Here we describe a method for fabricating human neural tissue by 3D printing human neural stem cells with a bioink
Weston B Struwe et al.
Cell reports, 24(8), 1958-1966 (2018-08-23)
Many broadly neutralizing antibodies (bnAbs) against HIV-1 recognize and/or penetrate the glycan shield on native, virion-associated envelope glycoprotein (Env) spikes. The same bnAbs also bind to recombinant, soluble trimeric immunogens based on the SOSIP design. While SOSIP trimers are close
Qingxin Cui et al.
Frontiers in pharmacology, 9, 948-948 (2018-09-07)
Purpose: Understanding the distribution and interaction of the Traditional Chinese Medicines (TCMs) is an integral source of herbal drug discovery. An optimized radio-labeled method was explored that could conduct in situ biodistribution studies in animals. We evaluated the feasibility of

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