image integration software nis-elements br Search Results


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Nikon nis elements imaging software v4 30
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Nikon digital sight camera nis-elements microscope imaging software
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Nikon imaging software nis element d ver.3
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Nikon eclipse ti e inverted microscope system
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Nikon digital analysis software nis-elements
Digital Analysis Software Nis Elements, 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
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Nikon nis-elements br imaging software
BSR-T7 cells were infected at an moi of 0.01 with the respective viruses. At 24 h p.i. cells were fixed and syncytia of the recombinant viruses were visualized by immunostaining using a hyperimmune serum against NDV. The syncytia sizes were determined by measuring the areas of 20 syncytia per virus in triplicate assays with <t>NIS-Elements</t> BR <t>imaging</t> <t>software.</t> All values are expressed relative to R75/98 which had been set as 100%. Error bars represent standard deviations. Significant differences (P<0.05, Bonferroni correction) between R75/98 and recombinant viruses are indicated (*).
Nis Elements Br Imaging 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
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Nikon imaging system (nis elements f 2.20 imaging software)
BSR-T7 cells were infected at an moi of 0.01 with the respective viruses. At 24 h p.i. cells were fixed and syncytia of the recombinant viruses were visualized by immunostaining using a hyperimmune serum against NDV. The syncytia sizes were determined by measuring the areas of 20 syncytia per virus in triplicate assays with <t>NIS-Elements</t> BR <t>imaging</t> <t>software.</t> All values are expressed relative to R75/98 which had been set as 100%. Error bars represent standard deviations. Significant differences (P<0.05, Bonferroni correction) between R75/98 and recombinant viruses are indicated (*).
Imaging System (Nis Elements F 2.20 Imaging 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
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Nikon nis elements software
BSR-T7 cells were infected at an moi of 0.01 with the respective viruses. At 24 h p.i. cells were fixed and syncytia of the recombinant viruses were visualized by immunostaining using a hyperimmune serum against NDV. The syncytia sizes were determined by measuring the areas of 20 syncytia per virus in triplicate assays with <t>NIS-Elements</t> BR <t>imaging</t> <t>software.</t> All values are expressed relative to R75/98 which had been set as 100%. Error bars represent standard deviations. Significant differences (P<0.05, Bonferroni correction) between R75/98 and recombinant viruses are indicated (*).
Nis Elements 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
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Average 90 stars, based on 1 article reviews
nis elements software - by Bioz Stars, 2026-04
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Nikon c1 fluorescent microscope
BSR-T7 cells were infected at an moi of 0.01 with the respective viruses. At 24 h p.i. cells were fixed and syncytia of the recombinant viruses were visualized by immunostaining using a hyperimmune serum against NDV. The syncytia sizes were determined by measuring the areas of 20 syncytia per virus in triplicate assays with <t>NIS-Elements</t> BR <t>imaging</t> <t>software.</t> All values are expressed relative to R75/98 which had been set as 100%. Error bars represent standard deviations. Significant differences (P<0.05, Bonferroni correction) between R75/98 and recombinant viruses are indicated (*).
C1 Fluorescent Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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c1 fluorescent microscope - by Bioz Stars, 2026-04
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Image Search Results


BSR-T7 cells were infected at an moi of 0.01 with the respective viruses. At 24 h p.i. cells were fixed and syncytia of the recombinant viruses were visualized by immunostaining using a hyperimmune serum against NDV. The syncytia sizes were determined by measuring the areas of 20 syncytia per virus in triplicate assays with NIS-Elements BR imaging software. All values are expressed relative to R75/98 which had been set as 100%. Error bars represent standard deviations. Significant differences (P<0.05, Bonferroni correction) between R75/98 and recombinant viruses are indicated (*).

Journal: PLoS ONE

Article Title: Different Regions of the Newcastle Disease Virus Fusion Protein Modulate Pathogenicity

doi: 10.1371/journal.pone.0113344

Figure Lengend Snippet: BSR-T7 cells were infected at an moi of 0.01 with the respective viruses. At 24 h p.i. cells were fixed and syncytia of the recombinant viruses were visualized by immunostaining using a hyperimmune serum against NDV. The syncytia sizes were determined by measuring the areas of 20 syncytia per virus in triplicate assays with NIS-Elements BR imaging software. All values are expressed relative to R75/98 which had been set as 100%. Error bars represent standard deviations. Significant differences (P<0.05, Bonferroni correction) between R75/98 and recombinant viruses are indicated (*).

Article Snippet: Photos were taken with a Nikon ECLIPSE Ti-S camera and evaluated with NIS-Elements BR imaging software, measuring the area of 20 syncytia per virus, with two repetitions.

Techniques: Infection, Recombinant, Immunostaining, Imaging, Software