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graphpad prism 8  (GraphPad Software Inc)


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  • 90

    Structured Review

    GraphPad Software Inc graphpad prism 8
    KEY RESOURCES TABLE
    Graphpad Prism 8, supplied by GraphPad Software Inc, 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/matlab+gui+program/graphpad+prism+software/pmc10154129-1148-221-226
    Average 90 stars, based on 1 article reviews
    graphpad prism 8 - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "D1 and D2 neurons in the nucleus accumbens enable positive and negative control over sugar intake in mice"

    Article Title: D1 and D2 neurons in the nucleus accumbens enable positive and negative control over sugar intake in mice

    Journal: Cell reports

    doi: 10.1016/j.celrep.2023.112190

    KEY RESOURCES TABLE
    Figure Legend Snippet: KEY RESOURCES TABLE

    Techniques Used: Plasmid Preparation, Recombinant, Injection, Software

    Related Articles

    Software:

    Article Title: Fibrotic scar formation after cerebral ischemic stroke: Targeting the Sonic hedgehog signaling pathway for scar reduction
    Article Snippet: .. GraphPad Prism software (version 9.0.0; GraphPad Software, Boston, MA, USA; www.graphpad.com ) was used for conducting statistical analyses. ..

    other:

    Article Title: TWEAK/Fn14 axis may promote vascular smooth muscle cell senescence via p38 signaling pathway: preliminary evidence.
    Article Snippet: Graphs of statistical analyses and calculations were plotted using GraphPad Prism 8.0 (GraphPad software, inc., la Jolla, ca, Usa).

    Article Title: Mesenchymal stem cell–derived small extracellular vesicles enhance the therapeutic effect of retinal progenitor cells in retinal degenerative disease rats
    Article Snippet: Graphical representations of the data were created using GraphPad Prism 8.0.1 for Windows (GraphPad Software, Boston, MA, USA, www.graphpad.com ).

    Article Title: In vitro digestion, cellular uptake and absorption of walnut protein-based nanoparticles mediated coenzyme Q10 nanosuspensions
    Article Snippet: Oral administration of Coenzyme Q10 (CoQ10) is hindered by its low bioaccessibility, and protein-based nanoparticles, commonly used to improve this, are vulnerable to degradation by pH, salts, and enzymes.. This study examined the in vitro digestion behavior and the subsequent cellular uptake and absorption of walnut protein-based nanoparticle-stabilized CoQ10 nanosuspensions (CQ@WPNP) to investigate their potential utility in addressing these challenges.. Cryo-electron microscopy (Cryo-EM), revealed structural rearrangements of CQ@WPNP during digestion, with both WPNP and CoQ10 nanoparticles remaining stable in the gastric phase, thereby preventing premature release.

    Article Title: Non-linear oral bioavailability and clinical pharmacokinetics of high-dose Andrographis paniculata ethanolic extract: relevant dosage implications for COVID-19 treatment.
    Article Snippet: Plasma concentration-time profiles in single and repeated doses were generated using GraphPad Prism 9.3.0 (GraphPad Software, USA).

    Article Title: Patients with idiopathic pulmonary fibrosis have fatty lungs impacting respiratory physiology.
    Article Snippet: The statistical analysis was completed using GraphPad Prism V10.2.3 (GraphPad Software Inc. La Jolla, CA, USA), with a p-value ≤0.05 considered statistically significant.

    Article Title: Epigenetic regulation of thrombo-inflammation in Behçet and antiphospholipid syndrome
    Article Snippet: Statistical analyses were performed using the Graph Pad Prism V.6.0 (GraphPad Software, San Diego, California, USA) and the software STATA version 14. p-values and adjusted p-values <0.05 (in overall analysis) were considered for statistical significance.

    Article Title: Long noncoding RNA GAS5 acts as a competitive endogenous RNA to regulate GSK-3β and PTEN expression by sponging miR-23b-3p in Alzheimer’s disease
    Article Snippet: One-way analysis of variance followed by Tukey’s post hoc test was performed to analyze statistical differences between multiple groups using GraphPad Prism software, version 8.0 (GraphPad Software, San Diego, CA, USA, www.graphpad.com ).



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    MathWorks Inc matlab-gui based program celltracker
    Study of migration of 2D cultured A549 cells in absence and presence of epidermal growth factor (EGF) and V-AgNPs at LD50-2D. (A) The schematic shows creation of cell-free area using cell inserts and addition of cell culture medium (control group), EGF (positive control group), and EGF + V-AgNPs (treatment group). Upon these treatments, the time lapse imaging was done to understand A549 cell migration in cell-free area using IncuCyte S3 live cell imaging platform. (B) The schematic shows the image analysis pipeline for time lapse images obtained from IncuCyte S3 instrument. The image analysis was done using our previously developed macro script for understanding % cell-free are over time as well as using a Matlab-GUI based <t>CellTracker</t> program for understanding cell migration pattern and migration velocities under various treatments. (C) The binary time lapse images obtained after image analysis show percent reduction of cell-free area (white area in the images) due to migration of A549 cells (black area in the images) in presence of only cell culture medium (black, upper row), EGF (blue, middle row), and EGF + V-AgNPs (red, lower row). The % cell-free areas were calculated by considering the cell-free area of 0 th h images as 100%. (D) The line graph shows the cell migration kinetics under the influence of various treatments, where each line represents mean ± std. error of 3 replicates ( n = 3). The yellow box indicates the time frame within which significant differences (two-way ANOVA, p-value <0.05) were observed in each treatment. The bar graph showing these differences is given in supporting information, . (E) The bar graph represents average cell migration velocities obtained from CellTracker program and each bar represents mean velocity ± std. error of randomly selected cells ( n = 10). The cell migration patterns and directionalities in presence of aforementioned treatments are given in the supporting information, . The asterisks in the bar graph represent significantly different observations (One-way ANOVA test: **** p-value<0.0001). (Abbreviations – V-AgNPs: Viridibacilli derived silver nanoparticles, EGF: Epidermal growth factor, t 0 : initial time or start time, t’: time point other that t 0 , h: hours, ns: not significant) (Schematics were created with BioRender.com ). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    Image Search Results


    Study of migration of 2D cultured A549 cells in absence and presence of epidermal growth factor (EGF) and V-AgNPs at LD50-2D. (A) The schematic shows creation of cell-free area using cell inserts and addition of cell culture medium (control group), EGF (positive control group), and EGF + V-AgNPs (treatment group). Upon these treatments, the time lapse imaging was done to understand A549 cell migration in cell-free area using IncuCyte S3 live cell imaging platform. (B) The schematic shows the image analysis pipeline for time lapse images obtained from IncuCyte S3 instrument. The image analysis was done using our previously developed macro script for understanding % cell-free are over time as well as using a Matlab-GUI based CellTracker program for understanding cell migration pattern and migration velocities under various treatments. (C) The binary time lapse images obtained after image analysis show percent reduction of cell-free area (white area in the images) due to migration of A549 cells (black area in the images) in presence of only cell culture medium (black, upper row), EGF (blue, middle row), and EGF + V-AgNPs (red, lower row). The % cell-free areas were calculated by considering the cell-free area of 0 th h images as 100%. (D) The line graph shows the cell migration kinetics under the influence of various treatments, where each line represents mean ± std. error of 3 replicates ( n = 3). The yellow box indicates the time frame within which significant differences (two-way ANOVA, p-value <0.05) were observed in each treatment. The bar graph showing these differences is given in supporting information, . (E) The bar graph represents average cell migration velocities obtained from CellTracker program and each bar represents mean velocity ± std. error of randomly selected cells ( n = 10). The cell migration patterns and directionalities in presence of aforementioned treatments are given in the supporting information, . The asterisks in the bar graph represent significantly different observations (One-way ANOVA test: **** p-value<0.0001). (Abbreviations – V-AgNPs: Viridibacilli derived silver nanoparticles, EGF: Epidermal growth factor, t 0 : initial time or start time, t’: time point other that t 0 , h: hours, ns: not significant) (Schematics were created with BioRender.com ). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Materials Today Bio

    Article Title: Viridibacillus culture derived silver nanoparticles exert potent anticancer action in 2D and 3D models of lung cancer via mitochondrial depolarization-mediated apoptosis

    doi: 10.1016/j.mtbio.2024.100997

    Figure Lengend Snippet: Study of migration of 2D cultured A549 cells in absence and presence of epidermal growth factor (EGF) and V-AgNPs at LD50-2D. (A) The schematic shows creation of cell-free area using cell inserts and addition of cell culture medium (control group), EGF (positive control group), and EGF + V-AgNPs (treatment group). Upon these treatments, the time lapse imaging was done to understand A549 cell migration in cell-free area using IncuCyte S3 live cell imaging platform. (B) The schematic shows the image analysis pipeline for time lapse images obtained from IncuCyte S3 instrument. The image analysis was done using our previously developed macro script for understanding % cell-free are over time as well as using a Matlab-GUI based CellTracker program for understanding cell migration pattern and migration velocities under various treatments. (C) The binary time lapse images obtained after image analysis show percent reduction of cell-free area (white area in the images) due to migration of A549 cells (black area in the images) in presence of only cell culture medium (black, upper row), EGF (blue, middle row), and EGF + V-AgNPs (red, lower row). The % cell-free areas were calculated by considering the cell-free area of 0 th h images as 100%. (D) The line graph shows the cell migration kinetics under the influence of various treatments, where each line represents mean ± std. error of 3 replicates ( n = 3). The yellow box indicates the time frame within which significant differences (two-way ANOVA, p-value <0.05) were observed in each treatment. The bar graph showing these differences is given in supporting information, . (E) The bar graph represents average cell migration velocities obtained from CellTracker program and each bar represents mean velocity ± std. error of randomly selected cells ( n = 10). The cell migration patterns and directionalities in presence of aforementioned treatments are given in the supporting information, . The asterisks in the bar graph represent significantly different observations (One-way ANOVA test: **** p-value<0.0001). (Abbreviations – V-AgNPs: Viridibacilli derived silver nanoparticles, EGF: Epidermal growth factor, t 0 : initial time or start time, t’: time point other that t 0 , h: hours, ns: not significant) (Schematics were created with BioRender.com ). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: Additionally, a Matlab-GUI based program called ‘CellTracker’ was also used to determine the directionality and average cell speed as per the instruction of developer [ ].

    Techniques: Migration, Cell Culture, Control, Positive Control, Imaging, Live Cell Imaging, Derivative Assay