Adhesion Protein Protocols

Cellular adhesion is a fundamental process that influences numerous biological activities such as morphogenesis, cell motility and division, as well as signalling. In addition, adhesion is a process important not only in normal physiology and development, but also in disease states such as tumourige...

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Chi tiết về thư mục
Tác giả của công ty: SpringerLink (Online service)
Tác giả khác: Coutts, Amanda S. (Biên tập viên, http://id.loc.gov/vocabulary/relators/edt)
Định dạng: Điện tử eBook
Ngôn ngữ:English
Được phát hành: Totowa, NJ : Humana Press : Imprint: Humana, 2013.
Phiên bản:3rd ed. 2013.
Loạt:Methods in Molecular Biology, 1046
Những chủ đề:
Truy cập trực tuyến:https://doi.org/10.1007/978-1-62703-538-5
Các nhãn: Thêm thẻ
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Mục lục:
  • Reconstructing Integrin Activation in vitro
  • Quantifying Cellular Adhesion to Covalently Immobilized Extracellular Matrix Proteins by Single-Force Spectroscopy
  • A Multimode-TIRFM & Microfluidic Technique to Examine Platelet Adhesion Dynamics
  • Localization-Based Super-Resolution Imaging of Cellular Structures
  • Use of Microarray Analysis to Investigate EMT Gene Signatures.-  Podosome Reformation in Macrophages: Assays and Analysis
  • Mobile and Three-Dimensional Presentation of Adhesion Proteins Within Microwells
  • Basement Membrane Invasion Assays: Native Basement Membrane and Chemoinvasion Assay
  • Cytoplasmic Actin: Purification and Single Molecule Assembly Assays
  • Synthetic and Tissue-Derived Models for Studying Rigidity Effects on Invadopodia Activity
  • Determining Rho GTPase Activity by an Affinity-Precipitation Assay
  • Proteomic and Biochemical Methods to Study the Cytoskeletome. Fabricating Surfaces with Distinct Geometries and Different Combinations of Cell Adhesion Proteins
  • Purification of Native Arp2/3 Complex from Bovine Thymus
  • Purification of Arp2/3 Complex from Saccharomyces Cerevisiae
  • Measurement and Analysis of in vitro Actin Polymerization
  • Use of the xCELLigence System for Real Time Analysis of changes in Cellular Motility and Adhesion in Physiological Conditions
  • Measuring Chemotaxis Using Direct Visualisation Microscope Chambers
  • In Vitro Microtubule Severing Assays
  • VE-Cadherin Status as an Indicator of Microvascular Permeability
  • High-Resolution Live-Cell Imaging and Time-Lapse Microscopy of Invadopodium Dynamics and Tracking Analysis
  • Live Cell Imaging of RhoGTPase Biosensors in Tumor Cells
  • Electrospun Nanofiber Scaffolds for Investigating Cell-matrix Adhesion
  • Method for Measuring Single-Molecule Adhesion Forces and Attachment Lifetimes of Protein-Membrane Interactions
  • VE-Cadherin Status as an Indicator of Microvascular Permeability
  • High-Resolution Live-Cell Imaging and Time-Lapse Microscopy of Invadopodium Dynamics and Tracking Analysis. Live Cell Imaging of RhoGTPase Biosensors in Tumor Cells
  • Electrospun Nanofiber Scaffolds for Investigating Cell-matrix Adhesion
  • Method for Measuring Single-Molecule Adhesion Forces and Attachment Lifetimes of Protein-Membrane Interactions.