Kinetic Assay for Quantification of Endocytosis of Cargos that Undergo Regulated Endocytosis
3:17
Post-acquisition Analysis
5:15
Population Analysis of Mup1-pHluorin Endocytosis by Flow Cytometry
7:37
Results: Quantitative, Kinetic, and High-throughput Analysis of Endocytosis of pHluorin-tagged Proteins
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Conclusion
副本
The overall goal of this procedure is to quantify vesicular trafficking events in the endocytic pathway of living cells. This method can help answer key questions in the vesicular trafficking field such as how mutation or changes in protein expres
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Accurate quantification of vesicular trafficking events often provides key insights into roles for specific proteins and the effects of mutations. This paper presents methods for using superecliptic pHluorin, a pH-sensitive GFP variant, as a tool for quantification of endocytic events in living cells using quantitative fluorescence microscopy and flow cytometry.