Stem cell bioengineering /

Written and edited by recognized experts in the field, the new Artech House Methods in Bioengineering book series offers detailed guidance on authoritative methods for addressing specific bioengineering challenges. Offering a highly practical presentation of each topic, each book provides research e...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Parekkadan, Biju, Yarmush, Martin L.
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Boston, Mass. ; London : Artech House, ©2009.
Colección:Artech House methods in bioengineering series.
Temas:
Stem cells.
Stem cells > Research.
Bioengineering.
Biomedical Engineering > methods
Stem Cells
Biotechnology
Cellules souches.
Cellules souches > Recherche.
Biotechnologie.
bioengineering.
MEDICAL > Research.
Acceso en línea:Texto completo
Tabla de Contenidos:
  • Methods in Bioengineering: Stem Cell Bioengineering; Contents; Preface; Chapter 1 Somatic Cell Nuclear Transfer and Derivation of Embryonic Stem Cells; 1.1 Introduction; 1.2 Materials for Nuclear Transfer; 1.2.1 Equipment for mouse nuclear transfer; 1.2.2 Reagents for mouse nuclear transfer; 1.3 Methods for Nuclear Transfer; 1.3.1 Preparation of enucleation and nuclear transfer pipettes; 1.3.2 Medium preparation; 1.3.3 Animal preparation; 1.3.4 Nuclear transfer; 1.3.5 Enucleation; 1.3.6 Preparation of donor cells; 1.3.7 Nuclear transfer; 1.3.8 Activation
  • 1.3.9 Embryo culture and embryo transfer1.4 Derivation of Mouse ntES Cells; 1.5 Materials for Embryonic Stem Cell Derivation; 1.6 Methods for Embryonic Stem Cell Derivation; 1.6.1 Derivation of ntES cells; 1.6.2 In vitro characterization of ntES cells; 1.6.3 In vivo characterization of ntES cells; 1.7 Discussion and Commentary; 1.8 Summary Points; Acknowledgments; References; Chapter 2 Derivation of Mouse Parthenogenetic Embryonic Stem Cells; 2.1 Introduction; 2.2 Materials; 2.2.1 Reagents; 2.2.2 Equipment; 2.2.3 Media recipe; 2.3 Methods; 2.3.1 Generation of p(MI) embryos
  • 2.3.2 Generation of p(MII) embryos2.3.3 Generation of p(hap) embryos; 2.3.4 Derivation of p(MI), p(MII), and p(hap) ES cells; 2.3.5 ES cell characterization; 2.3.6 Teratoma induction; 2.4 Data Acquisition, Anticipated Results, and Interpretation; 2.5 Discussion and Commentary; 2.6 Summary Points; Acknowledgments; References; Chapter 3 Generation of Mice from Embryonic Stem Cells Using Tetraploid Embryos as Hosts; 3.1 Introduction; 3.2 Experimental Design; 3.3 Materials; 3.3.1 Preparation of 4n embryos: Mice and reagents; 3.3.2 Preparation of 4n embryos: Equipment
  • 3.3.3 ES cells and culture conditions3.3.4 Micromanipulation system; 3.4 Methods; 3.4.1 Preparation of host embryos; 3.4.2 Electrofusion of two-cell stage embryos; 3.4.3 Removal of the zona pellucida; 3.4.4 Generation of ES multiple 4n embryos by aggregation; 3.4.5 Generation of ES 4n embryos by blastocyst injection; 3.4.6 Data acquisition; 3.5 Anticipated Results; 3.6 Discussion and Commentary; 3.7 Application Notes; 3.8 Summary Points; Acknowledgments; References; Chapter4 Bioreactor Design and Implementation; 4.1 Introduction; 4.2 Experimental Methods and Materials
  • 4.2.1 General system description4.2.2 Closed system; 4.2.3 Hollow-fiber bioreactor; 4.2.4 CES fluid circuit; 4.2.5 Oxygenator design; 4.2.6 Monitoring; 4.2.7 User interface; 4.3 Anticipated Results; 4.3.1 MSC source 1: Loading whole BM marrow into the CES; 4.3.2 MSC source 2 or 3: Loading preselected MSC into the CES; 4.4 Discussion and Commentary; 4.5 Application Notes; 4.5.1 Therapeutic dose of MSC grown from a whole BM sample; 4.5.2 Nonadherent cell culture: Kg1a cells grown in suspension; 4.6 Summary Points; Chapter 5 Extracellular Matrix Microarrays and Stem Cell Fate; 5.1 Introduction

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