Multiple Reaction Monitoring of mTRAQ-Labeled Peptides Enables Absolute Quantification of Endogenous Levels of a Potential Cancer Marker in Cancerous and Normal Endometrial Tissues-Reference-Cited by-同舟云学术

Multiple Reaction Monitoring of mTRAQ-Labeled Peptides Enables Absolute Quantification of Endogenous Levels of a Potential Cancer Marker in Cancerous and Normal Endometrial Tissues

Published:2008-07-17 Issue:8 Volume:7 Page:3525-3534
ISSN:1535-3893
Container-title:Journal of Proteome Research
language:en
Short-container-title:J. Proteome Res.

Author:

DeSouza Leroi V.¹,Taylor Adrian M.¹,Li Wei¹,Minkoff Marjorie S.¹,Romaschin Alexander D.¹,Colgan Terence J.¹,Siu K. W. Michael¹

Affiliation:

1. Department of Chemistry and Centre for Research in Mass Spectrometry, York University, Toronto, Ontario, Canada M3J 1P3, Applied Biosystems/MDS SCIEX, 71 Four Valley Drive, Concord, Ontario, Canada L4K 4V8, Applied Biosystems, 500 Old Connecticut Path, Framingham, Massachusetts 01701, Division of Clinical Biochemistry, St. Michael’s Hospital, 30 Bond Street, Toronto, Ontario, Canada M5B 1W8, Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada M5G 1L5, and...

Publisher

American Chemical Society (ACS)

Subject

General Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/pr800312m

Reference33 articles.

1. Multiplexed Protein Quantitation in Saccharomyces cerevisiae Using Amine-reactive Isobaric Tagging Reagents

2. Search for Cancer Markers from Endometrial Tissues Using Differentially Labeled Tags iTRAQ and cICAT with Multidimensional Liquid Chromatography and Tandem Mass Spectrometry

3. Endometrial Carcinoma Biomarker Discovery and Verification Using Differentially Tagged Clinical Samples with Multidimensional Liquid Chromatography and Tandem Mass Spectrometry

4. Verification of Endometrial Tissue Biomarkers Previously Discovered Using Mass Spectrometry-Based Proteomics by Means of Immunohistochemistry in a Tissue Microarray Format

5. Screening, confirmation, and quantification of sulphonamide residues in pig kidney by tandem mass spectrometry of crude extracts

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