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Cell-Based Assays Using iPSCs for Drug Development and Testing Second Edition 2025 [Hardback]

  • Formāts: Hardback, 271 pages, height x width: 254x178 mm, 61 Illustrations, color; 7 Illustrations, black and white; XIII, 271 p. 68 illus., 61 illus. in color., 1 Hardback
  • Sērija : Methods in Molecular Biology 2924
  • Izdošanas datums: 01-May-2025
  • Izdevniecība: Springer-Verlag New York Inc.
  • ISBN-10: 1071645293
  • ISBN-13: 9781071645291
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  • Formāts: Hardback, 271 pages, height x width: 254x178 mm, 61 Illustrations, color; 7 Illustrations, black and white; XIII, 271 p. 68 illus., 61 illus. in color., 1 Hardback
  • Sērija : Methods in Molecular Biology 2924
  • Izdošanas datums: 01-May-2025
  • Izdevniecība: Springer-Verlag New York Inc.
  • ISBN-10: 1071645293
  • ISBN-13: 9781071645291
Citas grāmatas par šo tēmu:

This up-to-date volume presents a set of differentiation and assay protocols useful to researchers involved in disease modeling, drug discovery, and the cell biology of a variety of tissues. The book begins with chapters on culture of induced pluripotent stem cells (iPSCs) and iPSC-derived cells with detailed protocols for culturing and differentiation of iPSC-derived endoderm, hepatocytes, vascular endothelial cells, cardiomyocytes, renal podocytes, neurons, and astrocytes. This is accompanied by newer protocols for the use of 3D cultures in assays adapted for drug development purposes, with new techniques such as high content analysis and microphysiological systems. Written for the highly successful Methods in Molecular Biology series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step and readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.

 

Authoritative and practical, Cell-Based Assays Using iPSCs for Drug Development and Testing, Second Edition serves as an ideal guide for scientists working to develop human iPSC-derived cellular models for drug discovery, efficacy, and safety purposes.

Cell-Based Assays Using Derived Human Induced Pluripotent Cells in Drug
Discovery and Development.- Using Human iPSC-Derived Astrocytes to
Investigate Transcription Factor-Driven Astrocyte to Neuron
Transdifferentiation.- Human Induced Pluripotent Stem Cell-Derived Definitive
Endoderm Bulk Up and Hepatic Differentiation.- One-Step Differentiation of
Human Induced Pluripotent Stem Cells into Podocytes.- Human Pluripotent Stem
Cell Expansion in Stirred Tank Bioreactors.- Co-Cultures of Human Induced
Pluripotent Stem Cell-Derived Neurons, Astrocytes, and Microglia for Modeling
Neurodegenerative Diseases.- A Robust Protocol for Pluripotent Stem Cell
Modeling of 3D Chamber-Like Cardiac Organoids.- Induced Pluripotent Stem
Cell-Derived Retinal Pigment Epithelial Cells for the Study of Macular
Degeneration.- Human Pluripotent Stem Cell-Derived Endothelial Cells in
Disease Modeling and Drug Screening.- Toxicity Testing Using Organoids Made
from Human Induced Pluripotent Stem Cells Engineered to Report Oxidative
Stress.- Modeling Human Liver Steatosis in Induced Pluripotent Stem
Cell-Derived Liver Spheres.- Utility of Induced Pluripotent Stem Cell-Based
Microphysiological Systems for Drug Development and Testing.- Compound
Testing of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Using
Multi-Well Microelectrode Arrays.- Methodology and Practice for Studying
Crosstalk between 3D Human Tissue Models in Pneumatically Actuated
Multi-Organ-on-Chip Systems.- Spheroid Formation and Easy and Stable Control
of Stromal Cells Using Multi-Inlet Spheroid Generator.- Engineered Hydrogels
for 3D Cell Culture and Bioprinting of Human Induced Pluripotent Stem
Cell-Derived Neuroepithelial Stem Cells.- A Non-Destructive, Image Analysis
Method for Evaluating Pigmentation in Induced Pluripotent Stem Cell-Derived
Retinal Pigment Epithelial Cells.- Evaluating the Effect of Drug Compounds on
Cardiac Spheroids Using the Cardiac Cell Outgrowth Assay in a
Microphysiological System.- High Content Analysis of Mitochondrial Function
in Induced Pluripotent Stem Cell-Derived Neurons.