- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1618-2650
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Reversed-phase separation methods for glycan analysis ; day:25 ; month:11 ; year:2016 ; pages:1-20
Analytical and bioanalytical chemistry ; (25.11.2016), 1-20
- Creator
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Vreeker, Gerda C. M.
- Contributor
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Wuhrer, Manfred
SpringerLink (Online service)
- DOI
-
10.1007/s00216-016-0073-0
- URN
-
urn:nbn:de:1111-2016121410507
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:59 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Vreeker, Gerda C. M.
- Wuhrer, Manfred
- SpringerLink (Online service)
Other Objects (12)
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A new strategy for the computer-assisted development of reversed-phase liquid chromatography separation methods of unknown sample mixtures
Methodenentwicklungen in der zweidimensionalen Reversed-Phase-Hochleistungsflüssigkeitschromatographie
Merging Solid‐Phase Peptide Synthesis and Automated Glycan Assembly to Prepare Lipid‐Peptide‐Glycan Chimeras
Cell-based glycan arrays for probing glycan–glycan binding protein interactions
Determination of polyolefin additives by reversed-phase liquid chromatography
Enzymatic Building‐Block Synthesis for Solid‐Phase Automated Glycan Assembly
Enzymatic Building‐Block Synthesis for Solid‐Phase Automated Glycan Assembly
Isomer Information from Ion Mobility Separation of High-Mannose Glycan Fragments
Separation of Molar Weight-Distributed Polyethylene Glycols by Reversed-Phase Chromatography—II. Preparative Isolation of Pure Single Homologs
Automated Glycan Assembly of 19 F‐labeled Glycan Probes Enables High‐Throughput NMR Studies of Protein–Glycan Interactions
Reversed-phase liquid-chromatographic mass spectrometric N-glycan analysis of biopharmaceuticals
Accelerated Solid Phase Glycan Synthesis: ASGS
A new strategy for the computer-assisted development of reversed-phase liquid chromatography separation methods of unknown sample mixtures
Methodenentwicklungen in der zweidimensionalen Reversed-Phase-Hochleistungsflüssigkeitschromatographie
Merging Solid‐Phase Peptide Synthesis and Automated Glycan Assembly to Prepare Lipid‐Peptide‐Glycan Chimeras
Cell-based glycan arrays for probing glycan–glycan binding protein interactions
Determination of polyolefin additives by reversed-phase liquid chromatography
Enzymatic Building‐Block Synthesis for Solid‐Phase Automated Glycan Assembly
Enzymatic Building‐Block Synthesis for Solid‐Phase Automated Glycan Assembly
Isomer Information from Ion Mobility Separation of High-Mannose Glycan Fragments
Separation of Molar Weight-Distributed Polyethylene Glycols by Reversed-Phase Chromatography—II. Preparative Isolation of Pure Single Homologs
Automated Glycan Assembly of 19 F‐labeled Glycan Probes Enables High‐Throughput NMR Studies of Protein–Glycan Interactions
Reversed-phase liquid-chromatographic mass spectrometric N-glycan analysis of biopharmaceuticals
Accelerated Solid Phase Glycan Synthesis: ASGS
A new strategy for the computer-assisted development of reversed-phase liquid chromatography separation methods of unknown sample mixtures
Methodenentwicklungen in der zweidimensionalen Reversed-Phase-Hochleistungsflüssigkeitschromatographie
Merging Solid‐Phase Peptide Synthesis and Automated Glycan Assembly to Prepare Lipid‐Peptide‐Glycan Chimeras
Cell-based glycan arrays for probing glycan–glycan binding protein interactions
Determination of polyolefin additives by reversed-phase liquid chromatography
Enzymatic Building‐Block Synthesis for Solid‐Phase Automated Glycan Assembly
Enzymatic Building‐Block Synthesis for Solid‐Phase Automated Glycan Assembly
Isomer Information from Ion Mobility Separation of High-Mannose Glycan Fragments
Separation of Molar Weight-Distributed Polyethylene Glycols by Reversed-Phase Chromatography—II. Preparative Isolation of Pure Single Homologs