dc.contributor.author |
Ngamsom, B
|
|
dc.contributor.author |
Fourie, L
|
|
dc.contributor.author |
Tarn, MD
|
|
dc.contributor.author |
Kumar, S
|
|
dc.contributor.author |
Moodley, K
|
|
dc.contributor.author |
Land, K
|
|
dc.contributor.author |
Pamme, N
|
|
dc.date.accessioned |
2017-04-10T10:32:36Z |
|
dc.date.available |
2017-04-10T10:32:36Z |
|
dc.date.issued |
2016-10 |
|
dc.identifier.citation |
Ngamsom, B., Fourie, L., Tarn, M.D., Kumar, S., Moodley, K., Land, K. and Pamme, N. 2016. Rapid detection of E. Coli O157:H7 by IFAST and ATP bioluminescence assay for water analysis. In: Proceedings of the 20th International Conference on Miniaturized Systems for Chemistry and Life Sciences (MicroTAS 2016), 9-13 October 2016, Dublin, Ireland |
en_US |
dc.identifier.isbn |
978-0-9798064-9-0 |
|
dc.identifier.uri |
http://hdl.handle.net/10204/8990
|
|
dc.description |
Proceedings of the 20th International Conference on Miniaturized Systems for Chemistry and Life Sciences (MicroTAS 2016), 9-13 October 2016, Dublin, Ireland |
en_US |
dc.description.abstract |
The present investigation reports isolation and detection of E. coli O157:H7 employing a simple and portable microfluidic device based on immiscible filtration assisted by surface tension (IFAST) and adenosine triphosphate (ATP) bioluminescence assay. The device demonstrated ca. 90% E. coli isolation with linear responses of bioluminescence signals from isolated cells at 6 – 600 CFU mL-1, suggesting great potential for point-of-need pathogenic bacteria detection for water analysis. |
en_US |
dc.language.iso |
en |
en_US |
dc.relation.ispartofseries |
Workflow;17850 |
|
dc.subject |
E. coli detection |
en_US |
dc.subject |
Water analysis |
en_US |
dc.subject |
Immiscible filtration assisted by surface tension |
en_US |
dc.subject |
IFAST |
en_US |
dc.subject |
Adenosine triphosphate |
en_US |
dc.subject |
ATP |
en_US |
dc.subject |
Microfluidics |
en_US |
dc.subject |
Microsystem |
en_US |
dc.subject |
Pathogen detection in water |
en_US |
dc.title |
Rapid detection of E. Coli O157:H7 by IFAST and ATP bioluminescence assay for water analysis |
en_US |
dc.type |
Conference Presentation |
en_US |
dc.identifier.apacitation |
Ngamsom, B., Fourie, L., Tarn, M., Kumar, S., Moodley, K., Land, K., & Pamme, N. (2016). Rapid detection of E. Coli O157:H7 by IFAST and ATP bioluminescence assay for water analysis. http://hdl.handle.net/10204/8990 |
en_ZA |
dc.identifier.chicagocitation |
Ngamsom, B, L Fourie, MD Tarn, S Kumar, K Moodley, K Land, and N Pamme. "Rapid detection of E. Coli O157:H7 by IFAST and ATP bioluminescence assay for water analysis." (2016): http://hdl.handle.net/10204/8990 |
en_ZA |
dc.identifier.vancouvercitation |
Ngamsom B, Fourie L, Tarn M, Kumar S, Moodley K, Land K, et al, Rapid detection of E. Coli O157:H7 by IFAST and ATP bioluminescence assay for water analysis; 2016. http://hdl.handle.net/10204/8990 . |
en_ZA |
dc.identifier.ris |
TY - Conference Presentation
AU - Ngamsom, B
AU - Fourie, L
AU - Tarn, MD
AU - Kumar, S
AU - Moodley, K
AU - Land, K
AU - Pamme, N
AB - The present investigation reports isolation and detection of E. coli O157:H7 employing a simple and portable microfluidic device based on immiscible filtration assisted by surface tension (IFAST) and adenosine triphosphate (ATP) bioluminescence assay. The device demonstrated ca. 90% E. coli isolation with linear responses of bioluminescence signals from isolated cells at 6 – 600 CFU mL-1, suggesting great potential for point-of-need pathogenic bacteria detection for water analysis.
DA - 2016-10
DB - ResearchSpace
DP - CSIR
KW - E. coli detection
KW - Water analysis
KW - Immiscible filtration assisted by surface tension
KW - IFAST
KW - Adenosine triphosphate
KW - ATP
KW - Microfluidics
KW - Microsystem
KW - Pathogen detection in water
LK - https://researchspace.csir.co.za
PY - 2016
SM - 978-0-9798064-9-0
T1 - Rapid detection of E. Coli O157:H7 by IFAST and ATP bioluminescence assay for water analysis
TI - Rapid detection of E. Coli O157:H7 by IFAST and ATP bioluminescence assay for water analysis
UR - http://hdl.handle.net/10204/8990
ER -
|
en_ZA |