ti e inverted fluorescence wide field microscope (Nikon)
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Nikon
ti e inverted fluorescence wide field microscope
Ti E Inverted Fluorescence Wide Field Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 59714 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ti-e+inverted+wide-field+fluorescence+microscope/Objectives/10__1038_slash_s42005___025___02392___8-265-9-8
Average 99 stars, based on 59714 article reviews
Ti E Inverted Fluorescence Wide Field Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 59714 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ti-e+inverted+wide-field+fluorescence+microscope/Objectives/10__1038_slash_s42005___025___02392___8-265-9-8
Average 99 stars, based on 59714 article reviews
ti e inverted fluorescence wide field microscope - by Bioz Stars,
2026-09
99/100 stars
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Imaging:Article Title: Contact lens-induced corneal parainflammation involving Ly6G+ cell infiltration requires IL-17A and γδ T cells. Article Snippet: Purpose: Previously, using a murine model, we reported that contact lens (CL) wear induced corneal parainflammation involving CD11c+ cells after 24 h and Ly6G+ cells (neutrophils) after 5–6 days.. Here, we investigated the role of IL-17 and γδ T cells in the CL-induced neutrophil response.. Methods: CL-wearing C57BL/6 wild-type (WT) mice were compared to lens-wearing IL-17A/F single or double gene knock-out mice, or mice treated with UC7-13D5 monoclonal antibody to functionally deplete γδ T cells. Article Title: TRPA1 and TPRV1 Ion Channels Are Required for Contact Lens-Induced Corneal Parainflammation and Can Modulate Levels of Resident Corneal Immune Cells. Article Snippet: Imaging corneal sections to observe Ly6G+ cells were performed using a Article Title: Pseudomonas aeruginosa can diversify after host cell invasion to establish multiple intracellular niches Article Snippet: Live and time-lapse images were captured on a Article Title: A novel murine model for contact lens wear reveals clandestine IL-1R dependent corneal parainflammation and susceptibility to microbial keratitis upon inoculation with Pseudomonas aeruginosa. Article Snippet: Sections were allowed to set for a minimum of 207 30 min before imaging using a Article Title: Improved yellow-green split fluorescent proteins for protein labeling and signal amplification. Article Snippet: Then cells were imaged on a Article Title: Bright split red fluorescent proteins for the visualization of endogenous proteins and synapses. Article Snippet: For SpyTag-sfCherry211 linked to the Nterminal of H2B, Article Title: A novel murine model for contact lens wear reveals clandestine IL-1R dependent corneal parainflammation and susceptibility to microbial keratitis upon inoculation with Pseudomonas aeruginosa Article Snippet: Sections were allowed to set for a minimum of 30 min before imaging using a Article Title: Pseudomonas aeruginosa Can Diversify after Host Cell Invasion to Establish Multiple Intracellular Niches Article Snippet: Live and time-lapse images were captured on a Fluorescence:Article Title: Contact lens-induced corneal parainflammation involving Ly6G+ cell infiltration requires IL-17A and γδ T cells. Article Snippet: Purpose: Previously, using a murine model, we reported that contact lens (CL) wear induced corneal parainflammation involving CD11c+ cells after 24 h and Ly6G+ cells (neutrophils) after 5–6 days.. Here, we investigated the role of IL-17 and γδ T cells in the CL-induced neutrophil response.. Methods: CL-wearing C57BL/6 wild-type (WT) mice were compared to lens-wearing IL-17A/F single or double gene knock-out mice, or mice treated with UC7-13D5 monoclonal antibody to functionally deplete γδ T cells. Article Title: TRPA1 and TPRV1 Ion Channels Are Required for Contact Lens-Induced Corneal Parainflammation and Can Modulate Levels of Resident Corneal Immune Cells. Article Snippet: Imaging corneal sections to observe Ly6G+ cells were performed using a Article Title: Pseudomonas aeruginosa can diversify after host cell invasion to establish multiple intracellular niches Article Snippet: Live and time-lapse images were captured on a Article Title: A novel murine model for contact lens wear reveals clandestine IL-1R dependent corneal parainflammation and susceptibility to microbial keratitis upon inoculation with Pseudomonas aeruginosa. Article Snippet: Sections were allowed to set for a minimum of 207 30 min before imaging using a Article Title: Improved yellow-green split fluorescent proteins for protein labeling and signal amplification. Article Snippet: Then cells were imaged on a Article Title: Bright split red fluorescent proteins for the visualization of endogenous proteins and synapses. Article Snippet: For SpyTag-sfCherry211 linked to the Nterminal of H2B, Article Title: A novel murine model for contact lens wear reveals clandestine IL-1R dependent corneal parainflammation and susceptibility to microbial keratitis upon inoculation with Pseudomonas aeruginosa Article Snippet: Sections were allowed to set for a minimum of 30 min before imaging using a Article Title: Pseudomonas aeruginosa Can Diversify after Host Cell Invasion to Establish Multiple Intracellular Niches Article Snippet: Live and time-lapse images were captured on a Microscopy:Article Title: Contact lens-induced corneal parainflammation involving Ly6G+ cell infiltration requires IL-17A and γδ T cells. Article Snippet: Purpose: Previously, using a murine model, we reported that contact lens (CL) wear induced corneal parainflammation involving CD11c+ cells after 24 h and Ly6G+ cells (neutrophils) after 5–6 days.. Here, we investigated the role of IL-17 and γδ T cells in the CL-induced neutrophil response.. Methods: CL-wearing C57BL/6 wild-type (WT) mice were compared to lens-wearing IL-17A/F single or double gene knock-out mice, or mice treated with UC7-13D5 monoclonal antibody to functionally deplete γδ T cells. Article Title: TRPA1 and TPRV1 Ion Channels Are Required for Contact Lens-Induced Corneal Parainflammation and Can Modulate Levels of Resident Corneal Immune Cells. Article Snippet: Imaging corneal sections to observe Ly6G+ cells were performed using a Article Title: Pseudomonas aeruginosa can diversify after host cell invasion to establish multiple intracellular niches Article Snippet: Live and time-lapse images were captured on a Article Title: A novel murine model for contact lens wear reveals clandestine IL-1R dependent corneal parainflammation and susceptibility to microbial keratitis upon inoculation with Pseudomonas aeruginosa. Article Snippet: Sections were allowed to set for a minimum of 207 30 min before imaging using a Article Title: Improved yellow-green split fluorescent proteins for protein labeling and signal amplification. Article Snippet: Then cells were imaged on a Article Title: Bright split red fluorescent proteins for the visualization of endogenous proteins and synapses. Article Snippet: For SpyTag-sfCherry211 linked to the Nterminal of H2B, Article Title: A novel murine model for contact lens wear reveals clandestine IL-1R dependent corneal parainflammation and susceptibility to microbial keratitis upon inoculation with Pseudomonas aeruginosa Article Snippet: Sections were allowed to set for a minimum of 30 min before imaging using a Article Title: Pseudomonas aeruginosa Can Diversify after Host Cell Invasion to Establish Multiple Intracellular Niches Article Snippet: Live and time-lapse images were captured on a Incubation:Article Title: Contact lens-induced corneal parainflammation involving Ly6G+ cell infiltration requires IL-17A and γδ T cells. Article Snippet: Purpose: Previously, using a murine model, we reported that contact lens (CL) wear induced corneal parainflammation involving CD11c+ cells after 24 h and Ly6G+ cells (neutrophils) after 5–6 days.. Here, we investigated the role of IL-17 and γδ T cells in the CL-induced neutrophil response.. Methods: CL-wearing C57BL/6 wild-type (WT) mice were compared to lens-wearing IL-17A/F single or double gene knock-out mice, or mice treated with UC7-13D5 monoclonal antibody to functionally deplete γδ T cells. Article Title: TRPA1 and TPRV1 Ion Channels Are Required for Contact Lens-Induced Corneal Parainflammation and Can Modulate Levels of Resident Corneal Immune Cells. Article Snippet: Imaging corneal sections to observe Ly6G+ cells were performed using a Article Title: Pseudomonas aeruginosa can diversify after host cell invasion to establish multiple intracellular niches Article Snippet: Live and time-lapse images were captured on a Article Title: A novel murine model for contact lens wear reveals clandestine IL-1R dependent corneal parainflammation and susceptibility to microbial keratitis upon inoculation with Pseudomonas aeruginosa. Article Snippet: Sections were allowed to set for a minimum of 207 30 min before imaging using a Article Title: Improved yellow-green split fluorescent proteins for protein labeling and signal amplification. Article Snippet: Then cells were imaged on a Article Title: Bright split red fluorescent proteins for the visualization of endogenous proteins and synapses. Article Snippet: For SpyTag-sfCherry211 linked to the Nterminal of H2B, Article Title: A novel murine model for contact lens wear reveals clandestine IL-1R dependent corneal parainflammation and susceptibility to microbial keratitis upon inoculation with Pseudomonas aeruginosa Article Snippet: Sections were allowed to set for a minimum of 30 min before imaging using a Article Title: Pseudomonas aeruginosa Can Diversify after Host Cell Invasion to Establish Multiple Intracellular Niches Article Snippet: Live and time-lapse images were captured on a Transfection:Article Title: Contact lens-induced corneal parainflammation involving Ly6G+ cell infiltration requires IL-17A and γδ T cells. Article Snippet: Purpose: Previously, using a murine model, we reported that contact lens (CL) wear induced corneal parainflammation involving CD11c+ cells after 24 h and Ly6G+ cells (neutrophils) after 5–6 days.. Here, we investigated the role of IL-17 and γδ T cells in the CL-induced neutrophil response.. Methods: CL-wearing C57BL/6 wild-type (WT) mice were compared to lens-wearing IL-17A/F single or double gene knock-out mice, or mice treated with UC7-13D5 monoclonal antibody to functionally deplete γδ T cells. Article Title: TRPA1 and TPRV1 Ion Channels Are Required for Contact Lens-Induced Corneal Parainflammation and Can Modulate Levels of Resident Corneal Immune Cells. Article Snippet: Imaging corneal sections to observe Ly6G+ cells were performed using a Article Title: Pseudomonas aeruginosa can diversify after host cell invasion to establish multiple intracellular niches Article Snippet: Live and time-lapse images were captured on a Article Title: A novel murine model for contact lens wear reveals clandestine IL-1R dependent corneal parainflammation and susceptibility to microbial keratitis upon inoculation with Pseudomonas aeruginosa. Article Snippet: Sections were allowed to set for a minimum of 207 30 min before imaging using a Article Title: Improved yellow-green split fluorescent proteins for protein labeling and signal amplification. Article Snippet: Then cells were imaged on a Article Title: Bright split red fluorescent proteins for the visualization of endogenous proteins and synapses. Article Snippet: For SpyTag-sfCherry211 linked to the Nterminal of H2B, Article Title: A novel murine model for contact lens wear reveals clandestine IL-1R dependent corneal parainflammation and susceptibility to microbial keratitis upon inoculation with Pseudomonas aeruginosa Article Snippet: Sections were allowed to set for a minimum of 30 min before imaging using a Article Title: Pseudomonas aeruginosa Can Diversify after Host Cell Invasion to Establish Multiple Intracellular Niches Article Snippet: Live and time-lapse images were captured on a |