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Prism v 4

Manufactured by IBM

Prism v.4 is a high-performance spectroscopy instrument designed for laboratory use. It features a compact and durable design, advanced optics, and precise measurement capabilities. The core function of Prism v.4 is to analyze the spectral properties of various materials and substances, providing accurate and reliable data for research and analysis purposes.

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Lab products found in correlation

3 protocols using prism v 4

1

Plasma Corticosterone, Thermoregulation, and c-Fos

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All data are reported as means±standard error of the mean (SEM). Data were analyzed using GraphPad Prism v.4 and SPSS v.16.0 software (Chicago, IL). For plasma corticosterone, body temperature, and c-Fos analyses, 2-way ANOVAs were utilized with drug treatment (MA, saline) and treatment period as between-subject factors. Bonferroni corrected post hoc comparisons were performed when statistically appropriate.
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2

Functional Connectivity Analyses in Neuroimaging

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All data are reported as means ± standard error of the mean (SEM). Data were analyzed using GraphPad Prism v.4 and SPSS v.16.0 software (Chicago, IL). Immunohistochemical data were analyzed using Two-Way ANOVA with time and treatment as factors. For the functional connectivity analyses, R software was used. Bonferroni corrected post hoc comparisons were performed when statistically appropriate. Using a bootstrapping procedure, we derived statistical significance for changes in the patterns of connectivity.
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3

Methamphetamine Effects on Stress Axes

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All data are reported as means ± standard error of the mean (SEM). Data were analyzed using GraphPad Prism v.4 and SPSS v.16.0 software (Chicago, IL). For the immunohistochemical analyses, data are presented as the number and percentage of c-Fos positive cells expressing GR or AVP. For corticosterone and body temperature analysis, 3-way ANOVA was utilized with treatment (MA, saline), sex (male, female), and time as between subject factors (0, 30, 70, 120 minutes). Immunohistochemical data (c-Fos, c-Fos/AVP, and c-Fos/GR) were analyzed using two-way ANOVA with sex and treatment as factors as well as separated by sex and analyzed as fold change compared to saline injection. Correlations between corticosterone and body temperature were performed using Spearman’s Rank Correlation Coefficient. Bonferroni corrected post hoc comparisons were performed when statistically appropriate. Student’s T-tests were utilized for comparison of fold increases in c-Fos and c-Fos/GR dual-labeled cells in MA compared to Saline treated mice.
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