Temporal-Lobe
发表于 2025-3-28 18:10:32
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Mobile
发表于 2025-3-28 21:23:06
Imaging and Analysis of Drosophila Neural Stem Cell Asymmetric Division,t the mechanisms that control cytoskeleton reorganization during asymmetric division. In this chapter, we propose to describe protocols that allow accurate analysis of microtubule reorganization during cell division in this model.
突袭
发表于 2025-3-29 01:11:16
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HUMID
发表于 2025-3-29 07:09:37
D. A. Ardus,D. Clare,J. M. Squireracts using fluorescence correlation spectroscopy (FCS), which measures the motions on a distance scale of ~200 nm. The method can also be used to characterize diffusion in the cytoplasm as it progresses through different phases of the cell cycle.
奖牌
发表于 2025-3-29 10:40:43
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photophobia
发表于 2025-3-29 15:03:31
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TRUST
发表于 2025-3-29 18:07:45
M. R. Cook,J. M. Squire,A. W. Hillidentified through mass spectrometry (MS) analyses using the APEX2 system; then a list of differentially phosphorylated proteins upon RIPPOs rapid degradation (achieved via the AID system) is compiled via SILAC phospho–mass spectrometry. The “in silico” overlap between the two proteomes will be enri
MOAT
发表于 2025-3-29 22:15:47
Mathematics and Its Applicationses obtained by AFM are in agreement with the ones previously obtained by micropipette aspiration. Our protocol could help characterize the biophysical properties of oocytes or other types of large nonadherent samples in fundamental and medical research.
得意牛
发表于 2025-3-30 02:53:07
https://doi.org/10.1007/978-94-017-2480-7mes during cell division. Here, we describe a technique based on injection of purified proteins that enables the visualization of microtubules and chromosomes with a high contrast in several divergent marine embryos. We also provide analysis methods and tools to extract microtubule dynamics and moni
健谈
发表于 2025-3-30 07:51:34
,Cell Cycle–Specific Protein Phosphatase 1 (PP1) Substrates Identification Using Genetically Modifieidentified through mass spectrometry (MS) analyses using the APEX2 system; then a list of differentially phosphorylated proteins upon RIPPOs rapid degradation (achieved via the AID system) is compiled via SILAC phospho–mass spectrometry. The “in silico” overlap between the two proteomes will be enri