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Tracking yeast pheromone receptor Ste2 endocytosis using fluorogen-activating protein tagging
To observe internalization of the yeast pheromone receptor Ste2 by fluorescence microscopy in live cells in real time, we visualized only those molecules present at the cell surface at the time of agonist engagement (rather than the total cellular pool) by tagging this receptor at its N-terminus wit...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Mol Biol Cell |
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| Κύριοι συγγραφείς: | , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
The American Society for Cell Biology
2018
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6249837/ https://ncbi.nlm.nih.gov/pubmed/30207829 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E18-07-0424 |
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