Abstract
A droplet-based high throughput platform was developed to screen single cell proteolytic enzymatic activity in a continuous flow manner, as a functional assay based flow cytometry (Droplet-FACS). With the capability to screen ~50 cells per second, whole primary tumor screening (~2x105 cells) was approached within 60 minutes to allow rapid profiling of patients' tumors based single cell multiplexed enzymatic assay. Moreover, the aggressive sub group of cancer cells could be identified and sorted for down-stream gene analysis.
| Original language | English |
|---|---|
| Title of host publication | μTAS 2017 |
| Subtitle of host publication | The 21st International Conference on Miniaturized Systems for Chemistry and Life Sciences |
| Publisher | Chemical and Biological Microsystems Society |
| Pages | 139-140 |
| ISBN (Electronic) | 9780692941836 |
| Publication status | Published - Oct 2017 |
| Externally published | Yes |
| Event | 21st International Conference on Miniaturized Systems for Chemistry and Life Sciences (MicroTAS 2017) - Savannah, United States Duration: 22 Oct 2017 → 26 Oct 2017 https://archive.cbmsociety.org/utas/uTAS2017.zip |
Publication series
| Name | International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS |
|---|---|
| Publisher | Chemical and Biological Microsystems Society |
| ISSN (Electronic) | 1556-5904 |
Conference
| Conference | 21st International Conference on Miniaturized Systems for Chemistry and Life Sciences (MicroTAS 2017) |
|---|---|
| Place | United States |
| City | Savannah |
| Period | 22/10/17 → 26/10/17 |
| Internet address |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Research Keywords
- Proteolytic activity assay
- Single cell analysis
- Whole tumor analysis
Fingerprint
Dive into the research topics of 'WHOLE TUMOR SCREENING WITH SINGLE CELL MULTIPLEXED PROTEOLYTIC ASSAY THROUGH CONTINUOUS FLOW MICROFLUIDICS'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver