虚度
发表于 2025-3-26 21:48:31
https://doi.org/10.1007/978-3-031-02613-3utilizing fluorescence microscopy to monitor the localization, and therefore the movement, of membrane-associated Atg proteins. We describe here a method that allows visualization of Atg membrane proteins in order to observe their potential source membranes and also to determine the temporal order o
gratify
发表于 2025-3-27 04:57:46
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提名
发表于 2025-3-27 07:44:49
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含糊
发表于 2025-3-27 11:02:35
1064-3745 hagosomal organelles. Comprehensive and forward-thinking, Autophagosome and Phagosome offers a valuable guide to both cellular processes while inciting researchers to explore the potentially important connections between the two..978-1-61737-806-5978-1-59745-157-4Series ISSN 1064-3745 Series E-ISSN 1940-6029
易弯曲
发表于 2025-3-27 17:02:48
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gerontocracy
发表于 2025-3-27 19:00:10
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SAGE
发表于 2025-3-28 01:43:00
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占线
发表于 2025-3-28 05:17:23
Microautophagy in the Yeast Saccharomyces cerevisiae, microautophagy only could be characterized microscopically. Recent studies provided the possibility to study the process in vitro and have identified the first molecules that are involved in microautophagy
一骂死割除
发表于 2025-3-28 08:32:52
Analysis of Phosphoinositide Dynamics During Phagocytosis Using Genetically Encoded Fluorescent Biogged probes (biosensors) into cultured macrophages. These biosensors are based on the fusion of phosphoinositide-binding protein domains with fluorescent proteins. Some specifications for live cell imaging of such phosphoinositide-specific probes are also provided.
HEW
发表于 2025-3-28 11:20:57
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