incubus 发表于 2025-3-23 12:34:52

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HAVOC 发表于 2025-3-23 15:16:16

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哀悼 发表于 2025-3-23 20:15:19

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宴会 发表于 2025-3-23 23:38:43

expansion is uniform across observable length scales, enabling imaging of structures previously too small to resolve. ExM is compatible with any microscope and does not require expensive materials or specialized software, offering effectively sub-diffraction-limited imaging capabilities to labs that

brachial-plexus 发表于 2025-3-24 04:33:20

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尖酸一点 发表于 2025-3-24 10:31:51

the exocytic vesicle networks, shuttle material in and out the cell, respectively. The substantial development of cell biological imaging techniques, along with improved fluorescent probes and image analysis tools, has been instrumental in increasing our understanding of various functions and regul

Esalate 发表于 2025-3-24 12:23:01

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acrimony 发表于 2025-3-24 16:56:26

a well-established model to study both processes. Recent studies show that a G-protein-coupled receptor (fAR1) mediate a signaling network to control reorganization of the actin cytoskeleton leading both the directional cell movement and the engulfment of bacteria. Many live cell imaging methods ha

abracadabra 发表于 2025-3-24 19:55:55

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paradigm 发表于 2025-3-25 02:23:21

es that directly or indirectly compromise cytoskeletal stability. While the large size and complexity of the neurons grown in culture poses certain challenges for imaging, live-cell imaging is an excellent approach to determine the morphological consequences of such mutants. This protocol details th
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查看完整版本: Titlebook: Confocal Microscopy; Methods and Protocol Joseph Brzostowski,Haewon Sohn Book 2021 This is a U.S. government work and not under copyright p