Macquarie Home | Course Handbook | Library | Campus Map | Macquarie Contacts
Home page

Macquarie University ResearchOnline

Home
Add
-List Of Titles -UV LED excited time-gated luminescence flow cytometry : evaluation for rare-event particle counting

Please use this identifier to cite or link to this item: http://hdl.handle.net/1959.14/141635

40 Visitors 46 Hits 3 Downloads
FileDescriptionSizeFormat
DS01Publisher version (open access)409 KBAdobe Acrobat PDFView/Open
Title
UV LED excited time-gated luminescence flow cytometry : evaluation for rare-event particle counting
Related
Imaging, manipulation, and analysis of biomolecules, cells, and tissues (6th : 2008) (21 - 23 January 2008 : San Jose, Calif.)
Related
Farkas, Daniel L.; Nicolau, Dan V. and Leif, Robert C.. Imaging, manipulation, and analysis of biomolecules, cells, and tissues VI : 21-23 January 2008, San Jose, California, USA
DOI
10.1117/12.762077
Related
SPIE proceedings series Vol. 6859
Publisher
Bellingham : SPIE
Date
2008
Author/Creator
Jin, Dayong
Author/Creator
Ferrari, Belinda
Author/Creator
Leif, Robert
Author/Creator
Yang, Sean
Author/Creator
Vallarino, Lidia M
Author/Creator
Williams, John
Author/Creator
Piper, James
Description
Flow cytometric detection of specific rare-event targets within high-background samples such as water or food are frequently defeated by the extremely large population of non-target background particles. Time-gated detection of long lifetime fluorescence (>10μs) labeled microbial targets has been proven highly efficient in suppressing this non-target autofluorescent (<0.1μs) background. A time-gated luminescence (TGL) flow cytometer using UV LED excitation has demonstrated the successful detection of rare-event particles in high autofluorescence background samples. In this report, high-quality 5μm europium beads were made (homogenous intensity and aggregation free) for a detailed evaluation of the prototype performance. The known number of beads (10±2, 100±20 and 1000±100) were first sorted by a conventional flow cytometry sorter, and spiked into an environmental water concentrate (1 ml; containing >10 million non-target particles). The recovery rate for counting these very-rare-event particles using the TGL flow cytometer was then found to be 100%±20% between bead concentrations evaluated.
Description
11 page(s)
Resource Type
conference paper
Organisation
Macquarie University. Dept. of Physics
Organisation
Macquarie University. Dept. of Chemistry and Biomolecular Sciences
Organisation
Macquarie University. Office of the Deputy Vice-Chancellor (Research)

Identifier
http://hdl.handle.net/1959.14/141635
Identifier
ISBN:9780819470348
Identifier
ISSN:0277-786X
Identifier
mq-rm-2008000588
Language
eng
Full Text
Full Text
 
Image Thumbnail
Save/E-mail Citation
Citation Format
E-mail Address
Subject
"Imaging, manipulation, and analysis of biomolecules, cells, and tissues VI : 21-23 January 2008, San Jose, California, USA"
 
OR
  • Show All  
  • Show My Selections 
Advanced Search

Search

Browse

  • By Title 
  • By Author/Creator 
  • By Department/Centre 
  • By Subject Keyword 
  • By Journal/Conference 
  • By FoR/RFCD codes 
  • By Resource Type 
  • By Date 

Highlights

  • Most Accessed Objects 
  • Recent Additions 
  • Pending Publications 
  • Author Profiles 

Resources

  • About ResearchOnline 
  • FAQ 
  • Open Access 
  • Open Access-FAQs 
  • Copyright 
  • Contribute 
  • Help 
  • Contact
  • Terms and Conditions 
Valid XHTML 1.0 Strict Powered by VITAL

Copyright Macquarie University | Privacy Statement | Accessibility Information

ABN 90 952 801 237 | CRICOS Provider No 00002J

Library Staff Sign In