Explore U2OS cell structural dynamics using Structured Illumination Microscopy (SIM) for detailed analysis. This study highlights the maximum intensity projection technique to enhance visualization of cellular components labeled with fluorescent markers.
Super-Resolution Imaging of U2OS Cells with SIM
Key Takeaways
- Research focus: SIM imaging of U2OS cells using fluorescent markers.
- Model system: U2OS cell line.
- Research goal: Enhance cell structural visualization with maximum intensity projections.
- Presented by: Unspecified; assume lab researcher collaboration.
- Content type: Scientific data visualization using microscopy.
SIM² Apotome: Comparison of widefield and SIM² Apotome single plane images of U2OS cells stained for actin (phalloidin Alexa Fluor 647, red), microtubules (anti-alpha-tubulin Alexa Fluor 488, green) and nuclei (Hoechst, blue).
Objective: LD LCI Plan-Apochromat 25× / 0.8 Imm Corr
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U2Os - Actin + Microtubules | Lattice SIM
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