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Direct real-time observation of actin filament branching mediated by Arp2/3 complex using total internal reflection fluorescence microscopy

Existing methods for studying actin filament dynamics have allowed analysis only of bulk samples or individual filaments after treatment with the drug phalloidin, which perturbs filament dynamics. Total internal reflection fluorescence microscopy with rhodamine-labeled actin allowed us to observe po...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Amann, Kurt J., Pollard, Thomas D.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: The National Academy of Sciences 2001
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC64974/
https://ncbi.nlm.nih.gov/pubmed/11742068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.211556398
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