Titlebook: Cytoskeleton Dynamics; Methods and Protocol Helder Maiato Book 2020 Springer Science+Business Media, LLC, part of Springer Nature 2020 micr

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Wendy K. Silverman,William M. Kurtinesgh-resolution live-cell microscopy in combination with π-EB1 photodissociation. However, these techniques are broadly applicable to other LOV2-based and likely other blue light-sensitive optogenetics. In addition to being a tool to investigate +TIP functions acutely and with subcellular resolution,

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Book 2020e an invaluable resource for present and future generations of cytoskeleton researchers. .The chapter “Visualization and Functional Analysis of Spindle Actin and Chromosome Segregation in Mammalian Oocytes” is available open access under a Creative Commons Attribution 4.0 International License via l

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https://doi.org/10.1007/978-1-4899-3567-0k-field microscopy. The ability to image microtubules label-free allows the investigation of the dynamic properties of non-abundant tubulin species where fluorescent labeling is not feasible, free from the confounding effects arising from the addition of fluorescent labels.

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重力

In Vitro Microtubule Dynamics Assays Using Dark-Field Microscopy,k-field microscopy. The ability to image microtubules label-free allows the investigation of the dynamic properties of non-abundant tubulin species where fluorescent labeling is not feasible, free from the confounding effects arising from the addition of fluorescent labels.

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