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dc.contributor.authorChen, WYen_US
dc.contributor.authorWang, LSen_US
dc.contributor.authorChiu, HTen_US
dc.contributor.authorChen, YCen_US
dc.contributor.authorLee, CYen_US
dc.date.accessioned2014-12-08T15:37:24Z-
dc.date.available2014-12-08T15:37:24Z-
dc.date.issued2004-11-01en_US
dc.identifier.issn1044-0305en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.jasms.2004.08.001en_US
dc.identifier.urihttp://hdl.handle.net/11536/25713-
dc.description.abstractRecently, carbon nanotubes (CNTs) have been reported to be an effective MALDI matrix for small molecules Anal. Chem 2003, 75, 6191). In a somewhat related study, we have employed CNTs produced by using NaH-treated anodic aluminum oxide (Na@AAO) as a reactive template as the assisting matrix for MALDI analysis upon the addition of high concentrations of citrate buffer. Our results indicate that the mass range can be extended to ca. 12,000 Da and that alkali metal adducts of analytes are effectively reduced. Furthermore, we have employed citric acid-treated CNTs as affinity probes to selectively concentrate traces of analytes from aqueous solutions. High concentrations of salts and surfactants in the sample solutions are also tolerated. This approach is very suitable for the MALDI analysis of small proteins, peptides, and protein enzymatic digest products. (J Am Soc Mass Spectrom 2004, 15, 1629-1635) (C) 2004 American Society for Mass Spectrometry.en_US
dc.language.isoen_USen_US
dc.titleCarbon nanotubes as affinity probes for peptides and proteins in MALDI MS analysisen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.jasms.2004.08.001en_US
dc.identifier.journalJOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRYen_US
dc.citation.volume15en_US
dc.citation.issue11en_US
dc.citation.spage1629en_US
dc.citation.epage1635en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000224925500012-
dc.citation.woscount58-
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