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Titlebook: Cell Migration in Three Dimensions; Coert Margadant Book 2023 The Editor(s) (if applicable) and The Author(s), under exclusive license to

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发表于 2025-3-21 19:41:08 | 显示全部楼层 |阅读模式
书目名称Cell Migration in Three Dimensions
编辑Coert Margadant
视频video
概述Includes cutting-edge techniques.Provides step-by-step detail essential for reproducible results.Contains key implementation advice from the experts
丛书名称Methods in Molecular Biology
图书封面Titlebook: Cell Migration in Three Dimensions;  Coert Margadant Book 2023 The Editor(s) (if applicable) and The Author(s), under exclusive license to
描述This detailed collection serves as a unique and excellent collection of state-of-the-art methods and protocols to interrogate cell migration in a wide variety of different contexts and model organisms, as well as advanced image analysis and quantitative assessment of a diverse array of parameters related to cell migration. The book focuses on the cell biology of cell migration, developmental model systems to assess cell migration during morphogenesis, cell migration in cancers and the tumor micro-environment, as well as blood vessel formation and interactions. 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 Migration in Three Dimensions. provides a solid foundation for scientists of different disciplines to investigate cell migration in biological processes. .Chapters 7, 12, 16, 17, 19, 22, and 24 are available open access under a Creative Commons Attribution 4.0 International License via link.springer.
出版日期Book 2023
关键词Model organisms; Morphogenesis; Tumor microenvironment; Blood vessel formation; Integrins; Filopodia
版次1
doihttps://doi.org/10.1007/978-1-0716-2887-4
isbn_softcover978-1-0716-2889-8
isbn_ebook978-1-0716-2887-4Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Busines
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Visualizing and Quantifying mRNA Localization at the Invasive Front of 3D Cancer Spheroidsade, and processed to image mRNAs with single-molecule sensitivity. An analysis algorithm is used to quantify and compare mRNA distributions at the front of invasive leader cells. The approach can be easily adapted and applied to analyze RNA distributions in additional settings where cells polarize along a linear axis.
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Obesity Management in Family Practiceating filopodia maps to compare the localization of multiple proteins within filopodia. Notably, while FiloMap was written to analyze filopodia, the analysis pipeline described here can also analyze and compile any line intensity profiles.
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Childhood and Adolescent Obesity,tact guidance studies. Then, we describe a method to perform the confinement on cells embedded inside a μm-thin 3D collagen gel. Finally, we describe an alternative method to confine cells based on agarose, so that cells can be fixed or drug perfused while being confined, which is currently not possible in the 2D confinement silicone-based device.
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Mapping the Localization of Proteins Within Filopodia Using FiloMapating filopodia maps to compare the localization of multiple proteins within filopodia. Notably, while FiloMap was written to analyze filopodia, the analysis pipeline described here can also analyze and compile any line intensity profiles.
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1064-3745 expertsThis detailed collection serves as a unique and excellent collection of state-of-the-art methods and protocols to interrogate cell migration in a wide variety of different contexts and model organisms, as well as advanced image analysis and quantitative assessment of a diverse array of param
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Visualization of Exosome Release and Uptake During Cell Migration Using the Live Imaging Reporter pHy encoded reporters of exosome secretion, pHluorin_M153R-CD63 and pHluorin_M153R-CD63-mScarlet. Here, we describe how to visualize secretion and uptake of exosomes labeled with these pH-sensitive and pH-insensitive fluorescent protein-tagged exosomal markers during cell migration using time-lapse fluorescent microscopy.
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