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Figure 4. Dose-dependent depletion of KSP from monopolar spindles in 1 and 5-treated cells. HeLa cells were incubated in either 1 (A–I) or 5 (J–R) for 4 h and the fixed and processed for KSP (green), the microtubule-binding protein <t>EB1</t> (red) and DNA (blue) localization, and images were acquired using equivalent exposure times for the green channel.
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Figure 4. Dose-dependent depletion of KSP from monopolar spindles in 1 and 5-treated cells. HeLa cells were incubated in either 1 (A–I) or 5 (J–R) for 4 h and the fixed and processed for KSP (green), the microtubule-binding protein <t>EB1</t> (red) and DNA (blue) localization, and images were acquired using equivalent exposure times for the green channel.
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Figure 4. Dose-dependent depletion of KSP from monopolar spindles in 1 and 5-treated cells. HeLa cells were incubated in either 1 (A–I) or 5 (J–R) for 4 h and the fixed and processed for KSP (green), the microtubule-binding protein <t>EB1</t> (red) and DNA (blue) localization, and images were acquired using equivalent exposure times for the green channel.
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Figure 4. Dose-dependent depletion of KSP from monopolar spindles in 1 and 5-treated cells. HeLa cells were incubated in either 1 (A–I) or 5 (J–R) for 4 h and the fixed and processed for KSP (green), the microtubule-binding protein <t>EB1</t> (red) and DNA (blue) localization, and images were acquired using equivalent exposure times for the green channel.
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Figure 4. Dose-dependent depletion of KSP from monopolar spindles in 1 and 5-treated cells. HeLa cells were incubated in either 1 (A–I) or 5 (J–R) for 4 h and the fixed and processed for KSP (green), the microtubule-binding protein <t>EB1</t> (red) and DNA (blue) localization, and images were acquired using equivalent exposure times for the green channel.
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Figure 4. Dose-dependent depletion of KSP from monopolar spindles in 1 and 5-treated cells. HeLa cells were incubated in either 1 (A–I) or 5 (J–R) for 4 h and the fixed and processed for KSP (green), the microtubule-binding protein <t>EB1</t> (red) and DNA (blue) localization, and images were acquired using equivalent exposure times for the green channel.
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Figure 4. Dose-dependent depletion of KSP from monopolar spindles in 1 and 5-treated cells. HeLa cells were incubated in either 1 (A–I) or 5 (J–R) for 4 h and the fixed and processed for KSP (green), the microtubule-binding protein <t>EB1</t> (red) and DNA (blue) localization, and images were acquired using equivalent exposure times for the green channel.
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Figure 4. Dose-dependent depletion of KSP from monopolar spindles in 1 and 5-treated cells. HeLa cells were incubated in either 1 (A–I) or 5 (J–R) for 4 h and the fixed and processed for KSP (green), the microtubule-binding protein <t>EB1</t> (red) and DNA (blue) localization, and images were acquired using equivalent exposure times for the green channel.
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Figure 4. Dose-dependent depletion of KSP from monopolar spindles in 1 and 5-treated cells. HeLa cells were incubated in either 1 (A–I) or 5 (J–R) for 4 h and the fixed and processed for KSP (green), the microtubule-binding protein <t>EB1</t> (red) and DNA (blue) localization, and images were acquired using equivalent exposure times for the green channel.
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Image Search Results


Figure 4. Dose-dependent depletion of KSP from monopolar spindles in 1 and 5-treated cells. HeLa cells were incubated in either 1 (A–I) or 5 (J–R) for 4 h and the fixed and processed for KSP (green), the microtubule-binding protein EB1 (red) and DNA (blue) localization, and images were acquired using equivalent exposure times for the green channel.

Journal: Bioorganic & Medicinal Chemistry

Article Title: Synthesis and characterization of tritylthioethanamine derivatives with potent KSP inhibitory activity

doi: 10.1016/j.bmc.2011.07.054

Figure Lengend Snippet: Figure 4. Dose-dependent depletion of KSP from monopolar spindles in 1 and 5-treated cells. HeLa cells were incubated in either 1 (A–I) or 5 (J–R) for 4 h and the fixed and processed for KSP (green), the microtubule-binding protein EB1 (red) and DNA (blue) localization, and images were acquired using equivalent exposure times for the green channel.

Article Snippet: Cells were then probed with either mouse anti-tubulin (Sigma, Co, St. Louis, MO), or mouse anti-KSP (Abcam, Cambridge, MA) in blocking buffer overnight at 4 C. To counterstain the microtubule cytoskeleton in KSP localization experiments, cells were also probed for the presence of the microtubule end-binding protein EB1 using a custom rabbit polyclonal antibody against whole recombinant human EB1 (Pro-Sci, Poway, CA).

Techniques: Incubation, Binding Assay