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Probst, Christopher: Microfluidic tools for single cell analysis. 2016
Inhalt
Title
Summary
Zusammenfassung
Table of Contents
List of Publications
List of Conference Proceedings
List of Posters
List of Patents
List of Abbreviations
List of Symbols
List of Figures
List of Tables
1 Industrial biotechnology
2 Population heterogeneity
3 Single cell analysis
4 Microfluidics
4.1 Theory
4.1.1 Convective mass transport
4.1.2 Diffusive mass transport
4.2 Fabrication of microfluidic devices
5 Microfluidic single cell analysis
5.1 Single cell trapping in microfluidics
5.1.1 Non-surface contact single-cell trapping
5.1.2 Surface contact single cell trapping mechanisms
Publications
6 Publication I - Polydimethylsiloxane (PDMS) Sub-Micron Traps for Single-Cell Analysis of Bacteria
6.1 Abstract
6.2 Introduction
6.3 Experimental
6.3.1 Soft Lithography
6.3.2 Sample Preparation
6.3.3 Experimental Procedure
6.4 Results and Discussion
6.4.1 Trap Layout and Geometry
6.4.2 Numerical Simulation
6.4.3 Single Cell Cultivation
6.5 Conclusions
7 Publication II - Spatiotemporal microbial single-cell analysis using a high-throughput microfluidics cultivation platform
7.1 Abstract
7.2 Introduction
7.3 Materials and Methods
7.3.1 Device fabrication and setup
7.3.2 Flow characterization
7.3.3 Bacterial strains and pre-cultivation
7.3.4 Microfluidic cultivation
7.3.5 Time-lapse imaging
7.3.6 Image analysis and data visualization
7.3.7 Flow cytometry (FC)
7.3.8 Computational fluid dynamics
7.4 Results
7.4.1 Device layout and principle
7.4.2 Flow tracer analysis
7.4.3 Computational fluid dynamics
7.4.4 Microbial single-cell analysis of isogenic microcolonies
7.4.5 Identifying rare cellular events in C. glutamicum
7.4.6 Dynamics of spontaneously induced SOS in single C. glutamicum cells
7.4.7 High-throughput screening of SOS+ cells
7.5 Discussion
7.6 Conclusions
7.7 Publication II Supplement
7.7.1 Publication II - Supplement 1
7.7.2 Publication II - Supplement 2
7.7.2.1 Frequency of spontaneously SOS+ induced cells at MGC at various gatings
7.7.2.2 Occurrence of spontaneously induced cells
7.7.3 Publication II - Supplement 3
7.7.3.1 Occurrence of spontaneously induced cells vs. total number of analyzed cells
7.7.3.2 Determination of SOS positive cells for FC measurements
8 Publication III - Rapid inoculation of single bacteria into parallel picoliter fermentation chambers
8.1 Abstract
8.2 Introduction
8.3 Materials and Methods
8.3.1 Chip fabrication
8.3.2 Device configuration
8.3.3 Experimental setup
8.3.4 Bubble injection and cell inoculation procedure
8.3.5 Fluorescent flow tracer analysis
8.3.6 Cultivation of C. glutamicum
8.4 Results and discussion
8.4.1 Single-cell inoculation procedure
8.4.2 Flow tracer characterization
8.4.3 Air bubble injection
8.4.4 Air bubble diffusion
8.4.5 Cell loading performance
8.4.6 Viability and cell growth
8.5 Conclusion
8.6 Publication III Supplement
8.6.1 Publication III - Capillary force calculation
8.6.2 Publication III - Fitting of experimental data
9 Publication IV - Microfluidic growth chambers with optical tweezers for full spatial single-cell control and analysis of evolving microbes
9.1 Abstract
9.2 Introduction
9.3 Materials and Methods
9.3.1 Fabrication of microfluidic growth chambers
9.3.2 Experimental microscopy setup
9.3.3 Cultivation of Escherichia coli
9.3.4 Cultivation in microfluidic chambers
9.3.5 Image analysis and data evaluation
9.3.6 Device principle and design
9.4 Results and Discussion
9.4.1 Growth in microenvironments
9.4.2 OT control over single cells
9.5 Conclusion and outlook
10 Future Perspectives
10.1 Batch cultivation in microfluidic devices
10.2 Flow control of liquids in microfluidic devices
10.2.1 Fabrication procedure of membrane pumps
10.2.1.1 Fabrication of microfluidic master molds
10.2.1.2 PDMS multilayer chip fabrication
10.2.2 Device design and principle
10.2.3 Experimental setup
10.2.4 Particle image velocimetry
10.2.5 Characterization of flow rates
10.2.6 Pulsation in flow
10.2.7 Conclusion and outlook
10.3 Control of oxygen levels in microfluidic devices
11 References
12 Supplemental information
12.1 Fabrication of multilayered microfluidic devices
12.1.1 Master mold fabrication
12.1.2 PDMS replica molding
12.2 Determination of pulsation rate
12.2.1 Rectangular shaped cross-section
12.2.2 Ellipsoid shaped cross-section
12.2.3 Coefficient of determination
12.3 Changing oxygen concentrations vs. flow rate