Preparation and chromatographic evaluation of a cysteine-bonded zwitterionic hydrophilic interaction liquid chromatography stationary phase.
about
A facilely synthesized amino-functionalized metal-organic framework for highly specific and efficient enrichment of glycopeptides.Highly efficient and selective enrichment of glycopeptides using easily synthesized magG/PDA/Au/l-Cys composites.Interaction modes and approaches to glycopeptide and glycoprotein enrichment.Stationary phases for the enrichment of glycoproteins and glycopeptides.Amino acids, peptides, and proteins as chemically bonded stationary phases--A review.The effect of solvation processes on amino acid- and peptide-silica stationary phases.Evaluation of separation properties of a modified strong cation exchange material named MEX and its application in 2D-MEX × C18 system to separate peptides from scorpion venom.Preparation of a novel carboxyl stationary phase by "thiol-ene" click chemistry for hydrophilic interaction chromatography.100% thiol-functionalized ethylene PMOs prepared by "thiol acid-ene" chemistry.Two-dimensional strong cation exchange/positively charged reversed-phase liquid chromatography for alkaloid analysis and purification.Preparation and evaluation of tert-leucine derivative functionalized polymeric monoliths for micro-liquid chromatography.Hydrogen-bonding dramatically modulates the gene transfection efficacy of surface-engineered dendrimers.Hydrophilic interaction liquid chromatography for the separation, purification, and quantification of raffinose family oligosaccharides from Lycopus lucidus Turcz.Purification of flavonoids from licorice using an off-line preparative two-dimensional normal-phase liquid chromatography/reversed-phase liquid chromatography method.Evaluation and application of a mixed-mode chromatographic stationary phase in two-dimensional liquid chromatography for the separation of traditional Chinese medicine.Novel imidazolium-embedded N,N-dimethylaminopropyl-functionalized silica-based stationary phase for hydrophilic interaction/reversed-phase mixed-mode chromatography.A New Stationary Phase for Hydrophilic Interaction Chromatography: Polyacrylate-Based Hydrophilic, Monosized-Porous Beads with Zwitterionic Molecular BrushesDetermination of N-Glycopeptides by Hydrophilic Interaction Liquid Chromatography and Porous Graphitized Carbon Chromatography with Mass Spectrometry Detection
P2860
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P2860
Preparation and chromatographic evaluation of a cysteine-bonded zwitterionic hydrophilic interaction liquid chromatography stationary phase.
description
2011 nî lūn-bûn
@nan
2011 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Preparation and chromatographi ...... romatography stationary phase.
@ast
Preparation and chromatographi ...... romatography stationary phase.
@en
Preparation and chromatographi ...... romatography stationary phase.
@nl
type
label
Preparation and chromatographi ...... romatography stationary phase.
@ast
Preparation and chromatographi ...... romatography stationary phase.
@en
Preparation and chromatographi ...... romatography stationary phase.
@nl
prefLabel
Preparation and chromatographi ...... romatography stationary phase.
@ast
Preparation and chromatographi ...... romatography stationary phase.
@en
Preparation and chromatographi ...... romatography stationary phase.
@nl
P2093
P1476
Preparation and chromatographi ...... romatography stationary phase.
@en
P2093
Aijin Shen
Xiaoming Cai
Xingya Xue
Xinmiao Liang
Zhimou Guo
P304
P356
10.1016/J.CHROMA.2011.10.086
P407
P577
2011-11-02T00:00:00Z