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Titlebook: Autophagy; Methods and Protocol Nicholas Ktistakis,Oliver Florey Book 2019 Springer Science+Business Media, LLC, part of Springer Nature 20

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51#
發(fā)表于 2025-3-30 11:08:00 | 只看該作者
52#
發(fā)表于 2025-3-30 14:59:47 | 只看該作者
53#
發(fā)表于 2025-3-30 18:42:52 | 只看該作者
An Ocean Bottom Absolute Gravity Meter identifying putative LIR motifs in a whole protein sequence using peptide arrays generated by SPOT synthesis on nitrocellulose membranes. The use of two-dimensional peptide arrays allows for further identification of specific residues critical for LIR binding.
54#
發(fā)表于 2025-3-30 21:28:05 | 只看該作者
Curvilinear Coordinates and General Tensors,and isolation membrane-associated tubules (IMATs). These methods can be easily applied to cultured mammalian cells for conventional and cutting-edge EM analyses, leading to a better understanding of ultrastructural details in autophagosome formation.
55#
發(fā)表于 2025-3-31 02:41:44 | 只看該作者
56#
發(fā)表于 2025-3-31 05:06:31 | 只看該作者
Recombinant Expression, Purification, and Assembly of p62 Filaments, as well as the preparation of negative stain EM grids to visualize the filaments. In vitro formed p62 filaments can be used to study receptor cargo interactions in minimal reconstituted autophagy model systems.
57#
發(fā)表于 2025-3-31 12:49:27 | 只看該作者
Biophysical Studies of LC3 Family Proteinsvesicles, (b) ultracentrifugation and fluorescence methods for assaying protein binding to membranes, and (c) procedures for assessing vesicle–vesicle aggregation and fusion. The latter include methods for intervesicular total lipid mixing, mixing of lipids in the vesicle inner monolayers, and aqueous contents mixing.
58#
發(fā)表于 2025-3-31 13:30:45 | 只看該作者
59#
發(fā)表于 2025-3-31 18:11:21 | 只看該作者
Improved Electron Microscopy Fixation Methods for Tracking Autophagy-Associated Membranes in Cultureand isolation membrane-associated tubules (IMATs). These methods can be easily applied to cultured mammalian cells for conventional and cutting-edge EM analyses, leading to a better understanding of ultrastructural details in autophagosome formation.
60#
發(fā)表于 2025-3-31 22:18:33 | 只看該作者
Methods for Imaging Autophagosome Dynamics in Primary Neuronsority of autophagosomes in dendrites are stationary, while some exhibit bidirectional movement. These studies establish an initial road map for autophagosome dynamics in each compartment of the neuron and set the stage for a more detailed understanding of neuronal autophagy in stress and disease.
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