olympus vs200 confocal microscope (Olympus)
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Olympus
olympus vs200 confocal microscope
Olympus Vs200 Confocal Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 99/100, based on 3317 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/olympus+vs200+confocal+microscope/VS200+Research+Slide+Scanner/pmc13011182-300-81-81
Average 99 stars, based on 3317 article reviews
Olympus Vs200 Confocal Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 99/100, based on 3317 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/olympus+vs200+confocal+microscope/VS200+Research+Slide+Scanner/pmc13011182-300-81-81
Average 99 stars, based on 3317 article reviews
olympus vs200 confocal microscope - by Bioz Stars,
2026-09
99/100 stars
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Staining:Article Title: Dual-Mode Aptamer AP1-F Achieves Molecular–Morphological Precision in Cancer Diagnostics via Membrane NCL Targeting Article Snippet: .. Images of all cells stained with AP1-F, AS1411-F, or Mut sequence-F (1 μM) were captured using an Article Title: Dual-Mode Aptamer AP1-F Achieves Molecular–Morphological Precision in Cancer Diagnostics via Membrane NCL Targeting Article Snippet: .. Images of all cells stained with AP1-F, AS1411-F, or Mut sequence-F (1 μM) were captured using an Article Title: A Unique G-Quadruplex Aptamer: A Novel Approach for Cancer Cell Recognition, Cell Membrane Visualization, and RSV Infection Detection. Article Snippet: .. Images of cancer cells and normal cells stained with Apt-3-F or AS1411-F (1 μM) were acquired using an Sequencing:Article Title: Dual-Mode Aptamer AP1-F Achieves Molecular–Morphological Precision in Cancer Diagnostics via Membrane NCL Targeting Article Snippet: .. Images of all cells stained with AP1-F, AS1411-F, or Mut sequence-F (1 μM) were captured using an Article Title: Dual-Mode Aptamer AP1-F Achieves Molecular–Morphological Precision in Cancer Diagnostics via Membrane NCL Targeting Article Snippet: .. Images of all cells stained with AP1-F, AS1411-F, or Mut sequence-F (1 μM) were captured using an Microscopy:Article Title: Dual-Mode Aptamer AP1-F Achieves Molecular–Morphological Precision in Cancer Diagnostics via Membrane NCL Targeting Article Snippet: .. Images of all cells stained with AP1-F, AS1411-F, or Mut sequence-F (1 μM) were captured using an Article Title: Customized ultra-flexible and adhesive spinal cord stimulation electrode for chronic pain management Article Snippet: For immunofluorescence, sections were blocked with 3% normal donkey serum (Jackson ImmunoResearch, Cat# 017-000-121) in PBST (0.3% Triton X-100) for 30 min at room temperature. .. Sections were incubated overnight at 4 °C with primary antibodies including rabbit anti-CD68 IgG (Proteintech, Cat# 83014-5-RR, 1:200), mouse anti-TNFα IgG (Proteintech, Cat# 60291-1-Ig, 1:100), or rabbit anti-Iba-1 IgG (FUJIFILM Wako, Cat# 019-19741, 1:500) and subsequently with donkey anti-mouse IgG secondary antibody conjugated with Alexa Fluor 488 (Jackson ImmunoResearch, Cat# 711-545-152, 1:500) or Donkey Anti-Rabbit IgG secondary antibody conjugated with Cy3 (Jackson ImmunoResearch, Cat# 711-165-152, 1:500) and DAPI (Beyotime, Cat# C1002, 1:10,000) for 2 h. Fluorescence imaging was conducted using an Article Title: Ultrasmall inorganic nanoparticles repair damaged meningeal lymphatic vessels to boost Parkinson's disease therapy. Article Snippet: .. The yellow arrows indicate the dCLNs. (C) In vivo second nearinfrared (NIR II) imaging of the neck of mice injected with neodymium- based nanoparticles to evaluate the drainage capability of their MLVs after laser ablation. (D) Quantitative subtraction of neck fluorescence intensity collected at 10, 20, and 30 min to assess the changes in drainage of dye from cervical lymph nodes. n = 3 (control group), 7 (laser ablation group), Mean ± SEM, Multiple t tests with Bonferroni Correction. (E) Representative immunofluorescence images of the transverse sinus of MLVs after 30 min injection of OVA- FITC. (Scale bar, 400 μm.) (F) OVA- FITC fluorescence areas on the meningeal lymphatic vessels (MLVs). n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (G) LYVE1 fluorescence areas on the MLVs. n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (H) Representative maximum- intensity projection images of MLVs acquired using an Article Title: Dual-Mode Aptamer AP1-F Achieves Molecular–Morphological Precision in Cancer Diagnostics via Membrane NCL Targeting Article Snippet: .. Images of all cells stained with AP1-F, AS1411-F, or Mut sequence-F (1 μM) were captured using an Article Title: A Unique G-Quadruplex Aptamer: A Novel Approach for Cancer Cell Recognition, Cell Membrane Visualization, and RSV Infection Detection. Article Snippet: .. Images of cancer cells and normal cells stained with Apt-3-F or AS1411-F (1 μM) were acquired using an Incubation:Article Title: Customized ultra-flexible and adhesive spinal cord stimulation electrode for chronic pain management Article Snippet: For immunofluorescence, sections were blocked with 3% normal donkey serum (Jackson ImmunoResearch, Cat# 017-000-121) in PBST (0.3% Triton X-100) for 30 min at room temperature. .. Sections were incubated overnight at 4 °C with primary antibodies including rabbit anti-CD68 IgG (Proteintech, Cat# 83014-5-RR, 1:200), mouse anti-TNFα IgG (Proteintech, Cat# 60291-1-Ig, 1:100), or rabbit anti-Iba-1 IgG (FUJIFILM Wako, Cat# 019-19741, 1:500) and subsequently with donkey anti-mouse IgG secondary antibody conjugated with Alexa Fluor 488 (Jackson ImmunoResearch, Cat# 711-545-152, 1:500) or Donkey Anti-Rabbit IgG secondary antibody conjugated with Cy3 (Jackson ImmunoResearch, Cat# 711-165-152, 1:500) and DAPI (Beyotime, Cat# C1002, 1:10,000) for 2 h. Fluorescence imaging was conducted using an Fluorescence:Article Title: Customized ultra-flexible and adhesive spinal cord stimulation electrode for chronic pain management Article Snippet: For immunofluorescence, sections were blocked with 3% normal donkey serum (Jackson ImmunoResearch, Cat# 017-000-121) in PBST (0.3% Triton X-100) for 30 min at room temperature. .. Sections were incubated overnight at 4 °C with primary antibodies including rabbit anti-CD68 IgG (Proteintech, Cat# 83014-5-RR, 1:200), mouse anti-TNFα IgG (Proteintech, Cat# 60291-1-Ig, 1:100), or rabbit anti-Iba-1 IgG (FUJIFILM Wako, Cat# 019-19741, 1:500) and subsequently with donkey anti-mouse IgG secondary antibody conjugated with Alexa Fluor 488 (Jackson ImmunoResearch, Cat# 711-545-152, 1:500) or Donkey Anti-Rabbit IgG secondary antibody conjugated with Cy3 (Jackson ImmunoResearch, Cat# 711-165-152, 1:500) and DAPI (Beyotime, Cat# C1002, 1:10,000) for 2 h. Fluorescence imaging was conducted using an Article Title: Ultrasmall inorganic nanoparticles repair damaged meningeal lymphatic vessels to boost Parkinson's disease therapy. Article Snippet: .. The yellow arrows indicate the dCLNs. (C) In vivo second nearinfrared (NIR II) imaging of the neck of mice injected with neodymium- based nanoparticles to evaluate the drainage capability of their MLVs after laser ablation. (D) Quantitative subtraction of neck fluorescence intensity collected at 10, 20, and 30 min to assess the changes in drainage of dye from cervical lymph nodes. n = 3 (control group), 7 (laser ablation group), Mean ± SEM, Multiple t tests with Bonferroni Correction. (E) Representative immunofluorescence images of the transverse sinus of MLVs after 30 min injection of OVA- FITC. (Scale bar, 400 μm.) (F) OVA- FITC fluorescence areas on the meningeal lymphatic vessels (MLVs). n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (G) LYVE1 fluorescence areas on the MLVs. n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (H) Representative maximum- intensity projection images of MLVs acquired using an Imaging:Article Title: Customized ultra-flexible and adhesive spinal cord stimulation electrode for chronic pain management Article Snippet: For immunofluorescence, sections were blocked with 3% normal donkey serum (Jackson ImmunoResearch, Cat# 017-000-121) in PBST (0.3% Triton X-100) for 30 min at room temperature. .. Sections were incubated overnight at 4 °C with primary antibodies including rabbit anti-CD68 IgG (Proteintech, Cat# 83014-5-RR, 1:200), mouse anti-TNFα IgG (Proteintech, Cat# 60291-1-Ig, 1:100), or rabbit anti-Iba-1 IgG (FUJIFILM Wako, Cat# 019-19741, 1:500) and subsequently with donkey anti-mouse IgG secondary antibody conjugated with Alexa Fluor 488 (Jackson ImmunoResearch, Cat# 711-545-152, 1:500) or Donkey Anti-Rabbit IgG secondary antibody conjugated with Cy3 (Jackson ImmunoResearch, Cat# 711-165-152, 1:500) and DAPI (Beyotime, Cat# C1002, 1:10,000) for 2 h. Fluorescence imaging was conducted using an Article Title: Ultrasmall inorganic nanoparticles repair damaged meningeal lymphatic vessels to boost Parkinson's disease therapy. Article Snippet: .. The yellow arrows indicate the dCLNs. (C) In vivo second nearinfrared (NIR II) imaging of the neck of mice injected with neodymium- based nanoparticles to evaluate the drainage capability of their MLVs after laser ablation. (D) Quantitative subtraction of neck fluorescence intensity collected at 10, 20, and 30 min to assess the changes in drainage of dye from cervical lymph nodes. n = 3 (control group), 7 (laser ablation group), Mean ± SEM, Multiple t tests with Bonferroni Correction. (E) Representative immunofluorescence images of the transverse sinus of MLVs after 30 min injection of OVA- FITC. (Scale bar, 400 μm.) (F) OVA- FITC fluorescence areas on the meningeal lymphatic vessels (MLVs). n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (G) LYVE1 fluorescence areas on the MLVs. n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (H) Representative maximum- intensity projection images of MLVs acquired using an Activation Assay:Article Title: Customized ultra-flexible and adhesive spinal cord stimulation electrode for chronic pain management Article Snippet: For immunofluorescence, sections were blocked with 3% normal donkey serum (Jackson ImmunoResearch, Cat# 017-000-121) in PBST (0.3% Triton X-100) for 30 min at room temperature. .. Sections were incubated overnight at 4 °C with primary antibodies including rabbit anti-CD68 IgG (Proteintech, Cat# 83014-5-RR, 1:200), mouse anti-TNFα IgG (Proteintech, Cat# 60291-1-Ig, 1:100), or rabbit anti-Iba-1 IgG (FUJIFILM Wako, Cat# 019-19741, 1:500) and subsequently with donkey anti-mouse IgG secondary antibody conjugated with Alexa Fluor 488 (Jackson ImmunoResearch, Cat# 711-545-152, 1:500) or Donkey Anti-Rabbit IgG secondary antibody conjugated with Cy3 (Jackson ImmunoResearch, Cat# 711-165-152, 1:500) and DAPI (Beyotime, Cat# C1002, 1:10,000) for 2 h. Fluorescence imaging was conducted using an In Vivo:Article Title: Ultrasmall inorganic nanoparticles repair damaged meningeal lymphatic vessels to boost Parkinson's disease therapy. Article Snippet: .. The yellow arrows indicate the dCLNs. (C) In vivo second nearinfrared (NIR II) imaging of the neck of mice injected with neodymium- based nanoparticles to evaluate the drainage capability of their MLVs after laser ablation. (D) Quantitative subtraction of neck fluorescence intensity collected at 10, 20, and 30 min to assess the changes in drainage of dye from cervical lymph nodes. n = 3 (control group), 7 (laser ablation group), Mean ± SEM, Multiple t tests with Bonferroni Correction. (E) Representative immunofluorescence images of the transverse sinus of MLVs after 30 min injection of OVA- FITC. (Scale bar, 400 μm.) (F) OVA- FITC fluorescence areas on the meningeal lymphatic vessels (MLVs). n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (G) LYVE1 fluorescence areas on the MLVs. n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (H) Representative maximum- intensity projection images of MLVs acquired using an Injection:Article Title: Ultrasmall inorganic nanoparticles repair damaged meningeal lymphatic vessels to boost Parkinson's disease therapy. Article Snippet: .. The yellow arrows indicate the dCLNs. (C) In vivo second nearinfrared (NIR II) imaging of the neck of mice injected with neodymium- based nanoparticles to evaluate the drainage capability of their MLVs after laser ablation. (D) Quantitative subtraction of neck fluorescence intensity collected at 10, 20, and 30 min to assess the changes in drainage of dye from cervical lymph nodes. n = 3 (control group), 7 (laser ablation group), Mean ± SEM, Multiple t tests with Bonferroni Correction. (E) Representative immunofluorescence images of the transverse sinus of MLVs after 30 min injection of OVA- FITC. (Scale bar, 400 μm.) (F) OVA- FITC fluorescence areas on the meningeal lymphatic vessels (MLVs). n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (G) LYVE1 fluorescence areas on the MLVs. n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (H) Representative maximum- intensity projection images of MLVs acquired using an Control:Article Title: Ultrasmall inorganic nanoparticles repair damaged meningeal lymphatic vessels to boost Parkinson's disease therapy. Article Snippet: .. The yellow arrows indicate the dCLNs. (C) In vivo second nearinfrared (NIR II) imaging of the neck of mice injected with neodymium- based nanoparticles to evaluate the drainage capability of their MLVs after laser ablation. (D) Quantitative subtraction of neck fluorescence intensity collected at 10, 20, and 30 min to assess the changes in drainage of dye from cervical lymph nodes. n = 3 (control group), 7 (laser ablation group), Mean ± SEM, Multiple t tests with Bonferroni Correction. (E) Representative immunofluorescence images of the transverse sinus of MLVs after 30 min injection of OVA- FITC. (Scale bar, 400 μm.) (F) OVA- FITC fluorescence areas on the meningeal lymphatic vessels (MLVs). n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (G) LYVE1 fluorescence areas on the MLVs. n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (H) Representative maximum- intensity projection images of MLVs acquired using an Immunofluorescence:Article Title: Ultrasmall inorganic nanoparticles repair damaged meningeal lymphatic vessels to boost Parkinson's disease therapy. Article Snippet: .. The yellow arrows indicate the dCLNs. (C) In vivo second nearinfrared (NIR II) imaging of the neck of mice injected with neodymium- based nanoparticles to evaluate the drainage capability of their MLVs after laser ablation. (D) Quantitative subtraction of neck fluorescence intensity collected at 10, 20, and 30 min to assess the changes in drainage of dye from cervical lymph nodes. n = 3 (control group), 7 (laser ablation group), Mean ± SEM, Multiple t tests with Bonferroni Correction. (E) Representative immunofluorescence images of the transverse sinus of MLVs after 30 min injection of OVA- FITC. (Scale bar, 400 μm.) (F) OVA- FITC fluorescence areas on the meningeal lymphatic vessels (MLVs). n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (G) LYVE1 fluorescence areas on the MLVs. n = 5 to 7, Mean ± SEM, one- way ANOVA with Dunnett’s multiple comparisons test. (H) Representative maximum- intensity projection images of MLVs acquired using an |