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nis-elements advanced research (ar) analysis software  (Nikon)

 
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    Nikon nis-elements advanced research (ar) analysis software
    Nis Elements Advanced Research (Ar) Analysis Software, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/nis-elements advanced research (ar) analysis software/product/Nikon
    Average 90 stars, based on 1 article reviews
    nis-elements advanced research (ar) analysis software - by Bioz Stars, 2026-03
    90/100 stars

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    Microglia activation in the hilus and piriform cortex of rats at 48 h after KA 11 mg/kg in saline, s. c. DMP 30 mg/kg 4 % PEG 4000, i. p. 30 min after KA and once/day until sacrificed. Microglial activation was measured by iba-1 immunostaining. Representative iba-1 immunostaining images, (A) hilus, (B) piriform <t>cortex.</t> <t>Fluorescence</t> image density quantification (C). Bars represent mean +S.D., n = 6 rats. Two-way ANOVA, *p < 0.01 KA + vehicle vs. control; #p < 0.01 KA + DMP vs. KA + vehicle. The average fluorescence intensity from vehicle group was expressed as 100 %. The fluorescence intensity was quantified with Nikon <t>NIS-Elements</t> Advanced image analysis software (version 4.6).
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    Microglia activation in the hilus and piriform cortex of rats at 48 h after KA 11 mg/kg in saline, s. c. DMP 30 mg/kg 4 % PEG 4000, i. p. 30 min after KA and once/day until sacrificed. Microglial activation was measured by iba-1 immunostaining. Representative iba-1 immunostaining images, (A) hilus, (B) piriform <t>cortex.</t> <t>Fluorescence</t> image density quantification (C). Bars represent mean +S.D., n = 6 rats. Two-way ANOVA, *p < 0.01 KA + vehicle vs. control; #p < 0.01 KA + DMP vs. KA + vehicle. The average fluorescence intensity from vehicle group was expressed as 100 %. The fluorescence intensity was quantified with Nikon <t>NIS-Elements</t> Advanced image analysis software (version 4.6).
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    Microglia activation in the hilus and piriform cortex of rats at 48 h after KA 11 mg/kg in saline, s. c. DMP 30 mg/kg 4 % PEG 4000, i. p. 30 min after KA and once/day until sacrificed. Microglial activation was measured by iba-1 immunostaining. Representative iba-1 immunostaining images, (A) hilus, (B) piriform <t>cortex.</t> <t>Fluorescence</t> image density quantification (C). Bars represent mean +S.D., n = 6 rats. Two-way ANOVA, *p < 0.01 KA + vehicle vs. control; #p < 0.01 KA + DMP vs. KA + vehicle. The average fluorescence intensity from vehicle group was expressed as 100 %. The fluorescence intensity was quantified with Nikon <t>NIS-Elements</t> Advanced image analysis software (version 4.6).
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    Image Search Results


    Microglia activation in the hilus and piriform cortex of rats at 48 h after KA 11 mg/kg in saline, s. c. DMP 30 mg/kg 4 % PEG 4000, i. p. 30 min after KA and once/day until sacrificed. Microglial activation was measured by iba-1 immunostaining. Representative iba-1 immunostaining images, (A) hilus, (B) piriform cortex. Fluorescence image density quantification (C). Bars represent mean +S.D., n = 6 rats. Two-way ANOVA, *p < 0.01 KA + vehicle vs. control; #p < 0.01 KA + DMP vs. KA + vehicle. The average fluorescence intensity from vehicle group was expressed as 100 %. The fluorescence intensity was quantified with Nikon NIS-Elements Advanced image analysis software (version 4.6).

    Journal: Redox Biology

    Article Title: Pharmacological elevation of glutathione inhibits status epilepticus-induced neuroinflammation and oxidative injury

    doi: 10.1016/j.redox.2024.103168

    Figure Lengend Snippet: Microglia activation in the hilus and piriform cortex of rats at 48 h after KA 11 mg/kg in saline, s. c. DMP 30 mg/kg 4 % PEG 4000, i. p. 30 min after KA and once/day until sacrificed. Microglial activation was measured by iba-1 immunostaining. Representative iba-1 immunostaining images, (A) hilus, (B) piriform cortex. Fluorescence image density quantification (C). Bars represent mean +S.D., n = 6 rats. Two-way ANOVA, *p < 0.01 KA + vehicle vs. control; #p < 0.01 KA + DMP vs. KA + vehicle. The average fluorescence intensity from vehicle group was expressed as 100 %. The fluorescence intensity was quantified with Nikon NIS-Elements Advanced image analysis software (version 4.6).

    Article Snippet: The fluorescence intensity was quantified with Nikon NIS-Elements Advanced image analysis software (version 4.6).

    Techniques: Activation Assay, Saline, Immunostaining, Fluorescence, Software

    Neuronal death in the hilus and piriform cortex of rats at 48 h after KA 11 mg/kg in saline s. c., DMP 30 mg/kg in 4 % PEG 4000, i. p. 30 min after KA and once/day until sacrificed. Neuronal death measured by Fluoro-Jade B staining. Representative Fluoro-Jade B staining images, (A) hilus, (B) piriform cortex. (C) Fluorescence image density quantification. Due to no significant positive staining in vehicle animals, the average FJB positive fluorescence density of KA + vehicle group were expressed as 100 %. Bars represent mean +S.D., n = 6 rats. Two-way ANOVA, *p < 0.01 KA + DMP vs. KA + vehicle. The average fluorescence intensity from KA + vehicle group was expressed as 100 %. The fluorescence intensity was quantified with Nikon NIS-Elements Advanced image analysis software (version 4.6).

    Journal: Redox Biology

    Article Title: Pharmacological elevation of glutathione inhibits status epilepticus-induced neuroinflammation and oxidative injury

    doi: 10.1016/j.redox.2024.103168

    Figure Lengend Snippet: Neuronal death in the hilus and piriform cortex of rats at 48 h after KA 11 mg/kg in saline s. c., DMP 30 mg/kg in 4 % PEG 4000, i. p. 30 min after KA and once/day until sacrificed. Neuronal death measured by Fluoro-Jade B staining. Representative Fluoro-Jade B staining images, (A) hilus, (B) piriform cortex. (C) Fluorescence image density quantification. Due to no significant positive staining in vehicle animals, the average FJB positive fluorescence density of KA + vehicle group were expressed as 100 %. Bars represent mean +S.D., n = 6 rats. Two-way ANOVA, *p < 0.01 KA + DMP vs. KA + vehicle. The average fluorescence intensity from KA + vehicle group was expressed as 100 %. The fluorescence intensity was quantified with Nikon NIS-Elements Advanced image analysis software (version 4.6).

    Article Snippet: The fluorescence intensity was quantified with Nikon NIS-Elements Advanced image analysis software (version 4.6).

    Techniques: Saline, Staining, Fluorescence, Software