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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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41#
發(fā)表于 2025-3-28 15:57:42 | 只看該作者
42#
發(fā)表于 2025-3-28 20:08:35 | 只看該作者
43#
發(fā)表于 2025-3-29 02:05:21 | 只看該作者
The Developmental Psychopathology of Anxietyellular function and integrity. However, their small size poses a challenge to study them. Here, we describe protocols that allow the identification and assessment of true centrioles and that provide straightforward strategies to study the role of new candidate proteins in centriole duplication and elongation.
44#
發(fā)表于 2025-3-29 05:39:44 | 只看該作者
Clinical Child Psychology Librarygregation in mammalian oocytes. To understand the function of spindle actin in oocyte meiosis, we have developed high-resolution and super-resolution live and immunofluorescence microscopy assays that are described in this chapter.
45#
發(fā)表于 2025-3-29 08:05:21 | 只看該作者
46#
發(fā)表于 2025-3-29 13:15:50 | 只看該作者
Processing TIRF Microscopy Images to Characterize the Dynamics and Morphology of Bacterial Actin-Liorphological properties of MreB assemblies. These include how to (1) segment bacterial cells, (2) perform single-particle tracking (SPT) of MreB filamentous structures, (3) classify their dynamic modes using mean squared displacement (MSD) analysis, and (4) measure their dimensions and orientation.
47#
發(fā)表于 2025-3-29 18:15:40 | 只看該作者
Studying Centriole Duplication and Elongation in Human Cells,ellular function and integrity. However, their small size poses a challenge to study them. Here, we describe protocols that allow the identification and assessment of true centrioles and that provide straightforward strategies to study the role of new candidate proteins in centriole duplication and elongation.
48#
發(fā)表于 2025-3-29 20:03:43 | 只看該作者
Visualization and Functional Analysis of Spindle Actin and Chromosome Segregation in Mammalian Oocygregation in mammalian oocytes. To understand the function of spindle actin in oocyte meiosis, we have developed high-resolution and super-resolution live and immunofluorescence microscopy assays that are described in this chapter.
49#
發(fā)表于 2025-3-30 02:00:53 | 只看該作者
Kwan Woo Choi,Yong-Ku Kim,Hong Jin Jeon, and the isolation of co-purifying tubulin-associated proteins (TAPs) in mammalian cells. This approach is currently used in our laboratory to study tubulin function and to identify and characterize TAPs.
50#
發(fā)表于 2025-3-30 07:23:15 | 只看該作者
Overview of Anxiety Management Trainingay enabling the characterization of Tau interaction with dynamic microtubules at the single-molecule level. We describe protein sample preparation in flow cells, single-molecule acquisitions by TIRF microscopy, and quantitative analysis of Tau oligomerization states and dwell time on microtubules.
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