Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | YOO, YS | - |
dc.contributor.author | KIM, YS | - |
dc.contributor.author | JHON, GJ | - |
dc.contributor.author | PARK, JS | - |
dc.date.accessioned | 2024-01-21T22:14:28Z | - |
dc.date.available | 2024-01-21T22:14:28Z | - |
dc.date.created | 2021-09-02 | - |
dc.date.issued | 1993-10-22 | - |
dc.identifier.issn | 0021-9673 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/145968 | - |
dc.description.abstract | Gangliosides are glycosphingolipids containing sialic acid. These glycolipids have been suggested to play important roles in biological processes such as cell growth, differentiation and malignant transformation. Based on these proposed biological functions, gangliosides can be used as diagnostic tools and therapeutics for various human diseases. In this study, capillary zone electrophoresis (CZE) was used to determine the major gangliosides G(M1), G(D1a), G(D1b) and G(T1b) in mammalian brains, in addition to G,, and Lac. Enhancement of selectivity and efficiency of separation was obtained by using 50 mM borate-phosphate buffer containing 16.5 mM alpha-cyclodextrin (alpha-CD). Under this condition, several forms of gangliosides were successfully separated from extracts of deer antler, apricot seed and rat brain. The results demonstrate that the CD-modified CZE is a useful method for detecting glycolipids from various biological matrices. | - |
dc.language | English | - |
dc.publisher | ELSEVIER SCIENCE BV | - |
dc.subject | PERFORMANCE LIQUID-CHROMATOGRAPHY | - |
dc.subject | ELECTROKINETIC CHROMATOGRAPHY | - |
dc.subject | MICELLAR | - |
dc.subject | ISOTACHOPHORESIS | - |
dc.subject | RESOLUTION | - |
dc.subject | PROTEINS | - |
dc.subject | BEHAVIOR | - |
dc.title | SEPARATION OF GANGLIOSIDES USING CYCLODEXTRIN IN CAPILLARY ZONE ELECTROPHORESIS | - |
dc.type | Article | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | JOURNAL OF CHROMATOGRAPHY A, v.652, no.2, pp.431 - 439 | - |
dc.citation.title | JOURNAL OF CHROMATOGRAPHY A | - |
dc.citation.volume | 652 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 431 | - |
dc.citation.endPage | 439 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | A1993MW22000017 | - |
dc.identifier.scopusid | 2-s2.0-0027366654 | - |
dc.relation.journalWebOfScienceCategory | Biochemical Research Methods | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Analytical | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | PERFORMANCE LIQUID-CHROMATOGRAPHY | - |
dc.subject.keywordPlus | ELECTROKINETIC CHROMATOGRAPHY | - |
dc.subject.keywordPlus | MICELLAR | - |
dc.subject.keywordPlus | ISOTACHOPHORESIS | - |
dc.subject.keywordPlus | RESOLUTION | - |
dc.subject.keywordPlus | PROTEINS | - |
dc.subject.keywordPlus | BEHAVIOR | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.