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Chapter Contents
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Book Title: Methods in Bioengineering: Nanoscale Bioengineering and Nanomedicine
Editors: Kaushal Rege, Arizona State University and Igor L. Medintz, U.S. Naval Research Laboratory
Chapter Contents: CH 1-2 | CH3-4 | CH5-6 | CH7-8 | CH9-10 | CH11-12 | CH12-13 | CH14-15 | CH16
Rege book cover
Methods in Bioengineering: Nanoscale Bioengineering and Nanomedicine
Kaushal Rege, Arizona State University and Igor L. Medintz, U.S. Naval Research Laboratory
ISBN: 978-1-59693-410-8
Copyright: 2009
Pages: 332
Price: $109/£66
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Chapter 5
Tracking Single Biomolecules in Live Cells using Quantum Dot Nanoparticles

5.1 spacer Introduction
5.2 Materials
5.2.1 Reagents
5.2.2 Imaging Equipment
5.3 Methods
5.3.1 Forming QD Bioconjugates
5.3.2 Treating cells with QD bioconjugates
5.4 Data Acquisition, Anticipated Results, and Interpretation
5.4.1 Imaging QD-bound complexes in cells
5.4.2 Analysis of the Real Time QD Dynamics
5.5 Discussion and Commentary
5.6 Troubleshooting Table
  References

Chapter 6
Designer Self-assembling Peptides Scaffolds for 3-dimensional Tissue Cell Cultures

6.1 spacer Introduction
6.1.1 Discovery and development of self-assembling peptide scaffold
6.1.2 The nanofiber structure of the peptide scaffold
6.1.3 A generic biological scaffold
6.1.4 Peptide scaffold fosters chondrocyte extracellular matrix production
6.1.5 Designer peptides appended with active motifs
6.2 Materials
6.3 Reagents
6.4 Methods
6.4.1 Peptide solution preparation
6.4.2 Designer peptide synthesis and scaffold preparation
6.4.3 Culture cells in plate inserts
6.4.4 Cell culture system
6.4.5 Neural cell culture and seeding
6.4.6 Preparation of MC3T3-E1 cells
6.4.7 Cell culture of human umbilical vein endothelial cells (HUVECs)
6.4.8 Cell proliferation assay
6.4.9 DNA content measurement
6.4.10 Boundary-sandwiched cell migration assay
6.4.11 Fluorescence microscopy
6.4.12 Immunocytochemistry
6.4.13 SEM sample preparation
6.4.14 Circular Dichroism (CD)
6.4.15 Structural study using atomic force microscopy (AFM)
6.4.16 Biomechanical study using rheology
6.4.17 Alkaline Phosphatase (ALP) staining for MC3T3-E1 cells
6.4.18 Biochemical assays for alkaline phosphatase (ALP) activity for MC3T3-E1 cells
6.4.19 Low protein release from the peptide scaffold
6.5 Data Acquisition, Results and Interpretation
6.5.1 Designer self-assembling peptide nanofiber hydrogel scaffold
6.5.2 3D cell cultures
6.5.3 Cell Migration in Peptide Scaffolds
6.5.4 Rheology of Peptide Hydrogel Scaffold
6.5.5 Tissue regeneration and tissue engineering
6.5.6 Protein releases from the peptide nanofiber hydrogel scaffold
6.6 Discussions and Commentary
6.7 Troubleshooting Table
6.8 Applications Notes
6.8.1 In vivo injectable self-assembling peptides
6.8.2 In vitro multi-cell system for tissue engineering
6.8.3 Mixed peptide hydrogel with polymer composites
6.9 Summary Points
  Acknowledgements
  Annotated References
  Supplementary Electronic Materials and Resources

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