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Sigmastat for windows 3

Manufactured by Grafiti LLC
Sourced in United States

SigmaStat for Windows 3.5 is a statistical analysis software package. It provides a range of statistical tests and data analysis tools for researchers and scientists. The software operates on the Windows 3.5 platform.

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10 protocols using sigmastat for windows 3

1

Quantitative Analysis of Iron and Hydroxyl Radicals

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The amount of nonchelated or reduced iron was calculated from the difference of absorbance between the tested sample (with ferrozine) and its corresponding blank (without ferrozine) divided by the difference of the control sample (the known amount of iron without the tested substance) and its control blank. The concentration of hydroxyl radical was calculated as the mean of the samples mixed (1) with methanol and (2) with added internal standards. Calculations in animal study were performed as previously described [6 (link)].
Grubb's test was used for detection of outlier values in animal and cell culture studies. Data were expressed as mean ± SD. For multiple comparisons, one-way ANOVA followed by Tukey's multiple comparisons test (in vivo experiments) and Bonferroni post hoc analysis (cell culture study) were used. Differences between groups were considered significant at P < 0.05 unless indicated otherwise. All statistical analyses were performed by GraphPad Prism version 6.0 for Windows (GraphPad Software, USA) except for the cell culture experiments where the statistical software SigmaStat for Windows 3.5 (Systat Software, Inc., USA) was used.
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2

Statistical Analysis of Experimental Data

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SigmaStat for Windows 3.5 (Systat Software, San Jose, CA, USA) statistical software package was utilized to analyze results. The data are expressed as the mean ± SD of a given number of experiments. Statistical significance was determined using a one-way ANOVA with a Bonferroni post-hoc test or Student’s t-test. The results were considered to be statistically significant when p < 0.05. The IC50 values were calculated using CalcuSyn 2.0 software (Biosoft, Cambridge, UK). Cell cycle analysis was evaluated using MultiCycle AV Software (Phoenix Flow Systems, San Diego, CA, USA).
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3

Catecholamine Toxicity Mitigation

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The statistical software SigmaStat for Windows 3.5 (Systat Software, CA, U.S.A.) and GraphPad Prism version 9 (GraphPad Software, San Diego USA) were used in this study. The Grubbs test was used for detection of outlier values. For comparisons of two groups, either Student’s t-test or the nonparametric Mann–Whitney rank sum test was used. For multiple comparisons, either one-way ANOVA with Bonferroni post hoc analysis or one-way ANOVA on ranks with Dunn's post hoc analysis (data without normal distribution) were used. Differences between groups were considered to be statistically significant at a significance level p ≤ 0.05. The concentrations of compounds under investigation inducing 50% protection of cellular viability from toxicity induced by catecholamines (EC50 values) were calculated with CalcuSyn 2.0 software (Biosoft, U.K.).
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4

Statistical Analysis of Experimental Groups

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For comparison of more than two groups, one-way Anova and multiple comparisons post-test according to the Holm-Sidak method was performed by using the software SigmaStat for Windows 3.5 (Systat Software, Inc., Erkrath, Germany). For the comparison of two groups, data were either analysed using paired t-test or Wilcoxon Signed Rank Test according to the distribution of the data. These statistical analyses were performed with the software GraphPad Prism version 5.0a. Asterisks in the figures indicate the p values: *p < 0.05, **p < 0.005 and ***p < 0.0005.
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5

Pharmacokinetics and Metabolic Effects of CBD

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All data, unless otherwise stated, are presented as mean and standard deviation. Statistical analyses were performed using dedicated, commercially available software (SigmaStat for Windows 3.5, Systat Software, Inc., Chicago, IL, USA). Differences in pharmacokinetic parameters between CBD formulations for CBD, and the CBD metabolites were explored using one-way analysis of variance (ANOVA) with repeated measures. Tukey’s tests were used to further examine the identified main effects. The thermic effect of food was examined using two-way ANOVA with repeated measures comparing energy expenditure across time for the two conditions (i.e., CBD and placebo); respiratory exchange ratio and circulating concentrations of glucose, insulin, and triglycerides were compared in the same way. The thermic effect of food was also examined by comparing the area under the curve (trapezoidal method) as previously described [29 (link),30 (link),36 (link)]. Circulating markers of liver and kidney function were compared across time and between CBD formulations using two-way ANOVA with repeated measures and post-hoc Tukey's tests when appropriate. Relations between circulating CBD concentrations and markers of liver and kidney function were explored using Pearson correlations. The level of statistical significance was set at p < 0.05.
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6

Calculating Molecular Properties Protocol

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The values of the molecular weights (MW) and n-octanol/water coefficients (log Pcalc; Table 2) were calculated using ChemBioOffice Ultra 11.0 software (CambridgeSoft, Cambridge, MA, USA). The log Pcalc is expressed as an average of the results of Crippen's [51] (link), Viswanadhan's [52] , and Broto's [53] method. SigmaStat for Windows 3.5 (Systat Software, San Jose, CA, USA) statistical software was used for data analyses. The data are expressed as the mean ±S.D. of at least 3 experiments. Statistical significance was determined using a one-way ANOVA with a Bonferroni post-hoc test (comparisons of multiple groups against the relevant control). The results were considered to be statistically significant when p<0.05. The EC50 (half-maximal effective concentration) and IC50 (half-maximal inhibitory concentration) values were calculated using CalcuSyn 2.0 software (Biosoft, Cambridge, UK). Raw data underlying the findings in this study are in Data S1.
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7

Quantitative Analyses of Embryonic Development

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All data are presented as mean ± SEM. Statistical analysis was performed using Sigma plot 8.0 for Windows and SigmaStat for Windows 3.0 (Systat Software, Inc., Chicago, US). N numbers refer to the number of examined animals, and all treatment regimes included in the analyses were performed at least 3 times (i.e. on at least 3 separate egg clutches).
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8

Statistical Data Analysis Protocol

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All data are presented as mean ± SEM. Statistical analysis and curve fitting were performed using Sigma plot 8.0 for Windows and SigmaStat for Windows 3.0 (Systat Software, Inc.). Statistical comparisons were made using Student’s t test or ANOVA when more than two groups were compared.
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9

Corneal Thickness and Dol Analysis

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Statistical analyses were conducted using SigmaStat for Windows 3.11
(Systat Software Inc., Point Richmond, CA). For each eye, the average
epithelial and stromal thicknesses, and Dol were calculated from the three
sections. The effect of treatment (vehicle or NM) was calculated using at
least 3 eyes. Comparisons between treatments were made using a one-way
Analysis of Variance, with P < 0.05 being considered significant.
Data are presented as mean ± SD.
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10

Epithelial and Stromal Dynamics

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Data were statistically analyzed using SigmaStat for Windows 3.11 (Systat Software Inc., Point Richmond, CA). Differences between materials based on EPA and GHS classifications for effects on epithelial and stromal DoI over time were detected using a two-way analysis of variance and the All Pairwise Multiple Comparisons test (Hom-Sidek method).
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