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QImaging qcapture suite plus software
Qcapture Suite Plus Software, supplied by QImaging, 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/product/eclipse+te2000+5+microscope/qcapture+software/pm33526718-164-22-16
Average 90 stars, based on 1 article reviews
qcapture suite plus software - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

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Article Title: Role of impulse oscillometry in chronic obstructive pulmonary disease and asthma-chronic obstructive pulmonary disease overlap.
Article Snippet: See the T erm s and C onditions (https://onlinelibrary.w iley.com /term s-and-conditions) on W iley O nline L ibrary for rules of use; O A articles are governed by the applicable C reative C om m ons L icense denoted by the mean linear intercept, was measured using a line grid in the QCapture Pro 6.0 software developed by QImaging Inc., headquartered in Surrey, British Columbia, Canada.

Article Title: Bioactive Composite Membranes: Preclinical Analysis of PBAT/BAGNb Composition to Enhance the Quality of Guided Bone Regeneration
Article Snippet: Slices were then imaged under 40× magnification (QCapture software, QImaging, British Columbia, Canada) for descriptive and quantitative analysis.

Article Title: Exposure to grassland fire ash alters the life-history traits and causes morphological deformities in the aquatic insect Chironomus xanthus.
Article Snippet: Wildfires generate large amounts of ash that can contaminate watercourses, with potentially harmful effects on aquatic biodiversity that are not fully understood.. This study experimentally evaluated the influence of environmentally relevant concentrations of grassland ash on aquatic biota, using the freshwater non-biting midge Chironomus xanthus as a model organism.. Specifically, we assessed the toxicity of ash on oviposition and emergence patterns, changes in body and head capsule sizes, and deformities in the mentum and mandible of 4th-instar larvae and the wings of adult C. xanthus.

Article Title: The STRIPAK complex is required for radial sorting and laminin receptor expression in Schwann cells
Article Snippet: Q-Capture Pro , QImaging, Inc , v7.0.4324.5.

Article Title: Bioactive Composite Membranes: Preclinical Analysis of PBAT/BAGNb Composition to Enhance the Quality of Guided Bone Regeneration.
Article Snippet: Staining with hematoxylin and eosin following washing and staining protocol.28 Slices were then imaged under 40× magnification (QCapture software, QImaging, British Columbia, Canada) for descriptive and quantitative analysis.

Article Title: Role of impulse oscillometry in chronic obstructive pulmonary disease and asthma‐chronic obstructive pulmonary disease overlap
Article Snippet: The air space size, as denoted by the mean linear intercept, was measured using a line grid in the QCapture Pro 6.0 software developed by QImaging Inc., headquartered in Surrey, British Columbia, Canada.

Software:

Article Title: A rat traumatized shoulder model for the study of post-surgical adhesions
Article Snippet: .. The individual assessment parameters included: (a) the presence and extent of the fibrous capsule adjacent to the periosteal injury site, measured by the mean of three widest measurement lines made using QCapture Pro 7 software (QImaging, Surrey, British Columbia, Canada), (b) presence and extent of necrosis, (c) tissue alterations within the cavity of implantation such as fragmentation, debris presence or foreign body granuloma formation, (d) signs of material residues (d) the extent of inflammation based on the number and types of inflammatory cells present next to the bone and (e) presence of macrophages and/or giant cells (i.e., layer of macrophages at the interface with the test material). .. Based on preliminary data from a few animals in a pilot study, assuming the shoulder range of motion of operated animals would 90 ± 12 degrees in the untreated control group and 120 ± 12 degrees in the alginate treated group, β = 0.2 (power 80 %), α = 0.05, 4 animals per group will be adequate (PROC POWER, SAS).



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(A) Representative <t>epifluorescence</t> images (20×) of L4 animals expressing Pins-3::GFP under basal conditions (20 °C on Nematode Growth Media plates seeded with OP50), under oxidative stress (1 mM FeSO 4, 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous tyramine (15 mM). Scale bar 50 µm. (B) Corresponding quantification of fluorescence levels per worm. Scatter dot plot with relative expression of Pins-3::GFP normalized to basal conditions of each independent experiment. Line at the median. n = 50−200 animals per condition (distributed across 3–4 independent experiments). One-way ANOVA and Dunn’s post hoc test vs. basal were used. * p < 0.05, **** p < 0.0001. (C) Log 2 fold-changes in ins-3 transcript levels in animals exposed to oxidative stress (1 mM FeSO 4 , 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous Tyramine (15 mM). Negative and positive values indicate down- and up-regulation of ins-3 , respectively. Fold change was calculated as ΔCt basal conditions/ΔCt test conditions. Results are shown as mean ± s.e.m. n = 4 independent experiments. The data underlying this figure can be found at https://osf.io/wfgvs/ .
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(A) Representative <t>epifluorescence</t> images (20×) of L4 animals expressing Pins-3::GFP under basal conditions (20 °C on Nematode Growth Media plates seeded with OP50), under oxidative stress (1 mM FeSO 4, 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous tyramine (15 mM). Scale bar 50 µm. (B) Corresponding quantification of fluorescence levels per worm. Scatter dot plot with relative expression of Pins-3::GFP normalized to basal conditions of each independent experiment. Line at the median. n = 50−200 animals per condition (distributed across 3–4 independent experiments). One-way ANOVA and Dunn’s post hoc test vs. basal were used. * p < 0.05, **** p < 0.0001. (C) Log 2 fold-changes in ins-3 transcript levels in animals exposed to oxidative stress (1 mM FeSO 4 , 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous Tyramine (15 mM). Negative and positive values indicate down- and up-regulation of ins-3 , respectively. Fold change was calculated as ΔCt basal conditions/ΔCt test conditions. Results are shown as mean ± s.e.m. n = 4 independent experiments. The data underlying this figure can be found at https://osf.io/wfgvs/ .
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Image Search Results


(A) Representative epifluorescence images (20×) of L4 animals expressing Pins-3::GFP under basal conditions (20 °C on Nematode Growth Media plates seeded with OP50), under oxidative stress (1 mM FeSO 4, 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous tyramine (15 mM). Scale bar 50 µm. (B) Corresponding quantification of fluorescence levels per worm. Scatter dot plot with relative expression of Pins-3::GFP normalized to basal conditions of each independent experiment. Line at the median. n = 50−200 animals per condition (distributed across 3–4 independent experiments). One-way ANOVA and Dunn’s post hoc test vs. basal were used. * p < 0.05, **** p < 0.0001. (C) Log 2 fold-changes in ins-3 transcript levels in animals exposed to oxidative stress (1 mM FeSO 4 , 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous Tyramine (15 mM). Negative and positive values indicate down- and up-regulation of ins-3 , respectively. Fold change was calculated as ΔCt basal conditions/ΔCt test conditions. Results are shown as mean ± s.e.m. n = 4 independent experiments. The data underlying this figure can be found at https://osf.io/wfgvs/ .

Journal: PLOS Biology

Article Title: The neurohormone tyramine stimulates the secretion of an insulin-like peptide from the Caenorhabditis elegans intestine to modulate the systemic stress response

doi: 10.1371/journal.pbio.3002997

Figure Lengend Snippet: (A) Representative epifluorescence images (20×) of L4 animals expressing Pins-3::GFP under basal conditions (20 °C on Nematode Growth Media plates seeded with OP50), under oxidative stress (1 mM FeSO 4, 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous tyramine (15 mM). Scale bar 50 µm. (B) Corresponding quantification of fluorescence levels per worm. Scatter dot plot with relative expression of Pins-3::GFP normalized to basal conditions of each independent experiment. Line at the median. n = 50−200 animals per condition (distributed across 3–4 independent experiments). One-way ANOVA and Dunn’s post hoc test vs. basal were used. * p < 0.05, **** p < 0.0001. (C) Log 2 fold-changes in ins-3 transcript levels in animals exposed to oxidative stress (1 mM FeSO 4 , 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous Tyramine (15 mM). Negative and positive values indicate down- and up-regulation of ins-3 , respectively. Fold change was calculated as ΔCt basal conditions/ΔCt test conditions. Results are shown as mean ± s.e.m. n = 4 independent experiments. The data underlying this figure can be found at https://osf.io/wfgvs/ .

Article Snippet: For ins-3 and ins-4 expression levels analysis, animals containing the corresponding transcriptional GFP reporter ( Pins-3::GFP and Pins-4:GFP , respectively) were imaged using an epifluorescence microscope (Nikon Eclipse TE2000-5) coupled to a CCD camera (Nikon DS-Qi2) with 20× objective.

Techniques: Expressing, Fluorescence

Representative epifluorescence images (40×) of young not gravid adults expressing Pges-1::INS-3::VENUS in wild-type and tyra-3 null mutant background, in the absence or presence of exogenous tyramine (15 mM). Scale bar 25 µm. Fluorescence is observed in the two posterior coelomocytes of worms (inset). Right. Corresponding quantification of fluorescence intensity on the coelomocytes (normalized to wild-type animals without tyramine exposure). Line at the median. n = 35–40 animals per condition distributed across three independent experiments. For conditions with tyramine, a two-tailed Student’s t test vs. the same strain without tyramine was used. * p < 0.05. The data underlying this figure can be found at https://osf.io/wfgvs/ .

Journal: PLOS Biology

Article Title: The neurohormone tyramine stimulates the secretion of an insulin-like peptide from the Caenorhabditis elegans intestine to modulate the systemic stress response

doi: 10.1371/journal.pbio.3002997

Figure Lengend Snippet: Representative epifluorescence images (40×) of young not gravid adults expressing Pges-1::INS-3::VENUS in wild-type and tyra-3 null mutant background, in the absence or presence of exogenous tyramine (15 mM). Scale bar 25 µm. Fluorescence is observed in the two posterior coelomocytes of worms (inset). Right. Corresponding quantification of fluorescence intensity on the coelomocytes (normalized to wild-type animals without tyramine exposure). Line at the median. n = 35–40 animals per condition distributed across three independent experiments. For conditions with tyramine, a two-tailed Student’s t test vs. the same strain without tyramine was used. * p < 0.05. The data underlying this figure can be found at https://osf.io/wfgvs/ .

Article Snippet: For ins-3 and ins-4 expression levels analysis, animals containing the corresponding transcriptional GFP reporter ( Pins-3::GFP and Pins-4:GFP , respectively) were imaged using an epifluorescence microscope (Nikon Eclipse TE2000-5) coupled to a CCD camera (Nikon DS-Qi2) with 20× objective.

Techniques: Expressing, Mutagenesis, Fluorescence, Two Tailed Test