anova for multiple comparisons tests Search Results


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GraphPad Software Inc anova with a post hoc bonferroni multiple-comparison test or two tailed t-tests prism 3.0
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GraphPad Software Inc one and two-way anova multiple comparisons with graphpad prism 9.3.1
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GraphPad Software Inc ordinary one-way anova with holm–sidak correction for multiple comparisons
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GraphPad Software Inc repeated measures one-way anova and tukey’s multiple comparison post hoc test functions
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GraphPad Software Inc nonparametric anova with dunn multiple comparison posttest using graphpad instat software
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SAS institute anova with duncan multiple range test
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SYSTAT one way analysis of variance tests with dunnett’s post hoc test
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GraphPad Software Inc anova with sidak’s multiple comparisons graphpad prism version 9
(A) Images represent calcofluor white (CFW) staining of WT CEA10, Δ zfpA , and OE:: zfpA following overnight exposure to 1 μg/mL caspofungin (CSP) or DMSO. CFW staining is represented by cyan and cytoplasmic RFP signal is shown in magenta. Scale bar = 50 μm. (B) Experimental setup for chitin stimulation with CaCl 2 /CFW. Spores were incubated for 8 h at 37°C or until germination in liquid GMM or liquid GMM supplemented with 0.2 M CaCl 2 and 100 μg/mL CFW. After germination, media was replaced for GMM + 1 μg/mL caspofungin or DMSO and hyphae were incubated for an additional 12 h before detecting PrestoBlue viability reagent signal in a plate reader. (C) Bars represent mean±s.d. of relative fungal viability following caspofungin exposure. Relative viability was calculated by normalizing the mean signal of caspofungin-treated wells to the mean signal of DMSO-treated wells. All experiments included 5 wells/condition. Data are pooled from 3 independent experiments. p values calculated by ANOVA with <t>Sidak’s</t> multiple comparisons. ** p <0.01,*** p <0.001.
Anova With Sidak’s Multiple Comparisons Graphpad Prism Version 9, 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
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Average 90 stars, based on 1 article reviews
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SAS institute anovas followed by smm multiple comparison procedure
(A) Images represent calcofluor white (CFW) staining of WT CEA10, Δ zfpA , and OE:: zfpA following overnight exposure to 1 μg/mL caspofungin (CSP) or DMSO. CFW staining is represented by cyan and cytoplasmic RFP signal is shown in magenta. Scale bar = 50 μm. (B) Experimental setup for chitin stimulation with CaCl 2 /CFW. Spores were incubated for 8 h at 37°C or until germination in liquid GMM or liquid GMM supplemented with 0.2 M CaCl 2 and 100 μg/mL CFW. After germination, media was replaced for GMM + 1 μg/mL caspofungin or DMSO and hyphae were incubated for an additional 12 h before detecting PrestoBlue viability reagent signal in a plate reader. (C) Bars represent mean±s.d. of relative fungal viability following caspofungin exposure. Relative viability was calculated by normalizing the mean signal of caspofungin-treated wells to the mean signal of DMSO-treated wells. All experiments included 5 wells/condition. Data are pooled from 3 independent experiments. p values calculated by ANOVA with <t>Sidak’s</t> multiple comparisons. ** p <0.01,*** p <0.001.
Anovas Followed By Smm Multiple Comparison Procedure, supplied by SAS institute, 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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Image Search Results


(A) Images represent calcofluor white (CFW) staining of WT CEA10, Δ zfpA , and OE:: zfpA following overnight exposure to 1 μg/mL caspofungin (CSP) or DMSO. CFW staining is represented by cyan and cytoplasmic RFP signal is shown in magenta. Scale bar = 50 μm. (B) Experimental setup for chitin stimulation with CaCl 2 /CFW. Spores were incubated for 8 h at 37°C or until germination in liquid GMM or liquid GMM supplemented with 0.2 M CaCl 2 and 100 μg/mL CFW. After germination, media was replaced for GMM + 1 μg/mL caspofungin or DMSO and hyphae were incubated for an additional 12 h before detecting PrestoBlue viability reagent signal in a plate reader. (C) Bars represent mean±s.d. of relative fungal viability following caspofungin exposure. Relative viability was calculated by normalizing the mean signal of caspofungin-treated wells to the mean signal of DMSO-treated wells. All experiments included 5 wells/condition. Data are pooled from 3 independent experiments. p values calculated by ANOVA with Sidak’s multiple comparisons. ** p <0.01,*** p <0.001.

Journal: bioRxiv

Article Title: Aspergillus fumigatus transcription factor ZfpA regulates hyphal development and alters susceptibility to antifungals and neutrophil killing during infection

doi: 10.1101/2023.01.25.525624

Figure Lengend Snippet: (A) Images represent calcofluor white (CFW) staining of WT CEA10, Δ zfpA , and OE:: zfpA following overnight exposure to 1 μg/mL caspofungin (CSP) or DMSO. CFW staining is represented by cyan and cytoplasmic RFP signal is shown in magenta. Scale bar = 50 μm. (B) Experimental setup for chitin stimulation with CaCl 2 /CFW. Spores were incubated for 8 h at 37°C or until germination in liquid GMM or liquid GMM supplemented with 0.2 M CaCl 2 and 100 μg/mL CFW. After germination, media was replaced for GMM + 1 μg/mL caspofungin or DMSO and hyphae were incubated for an additional 12 h before detecting PrestoBlue viability reagent signal in a plate reader. (C) Bars represent mean±s.d. of relative fungal viability following caspofungin exposure. Relative viability was calculated by normalizing the mean signal of caspofungin-treated wells to the mean signal of DMSO-treated wells. All experiments included 5 wells/condition. Data are pooled from 3 independent experiments. p values calculated by ANOVA with Sidak’s multiple comparisons. ** p <0.01,*** p <0.001.

Article Snippet: Comparison of fungal viability in was done using ANOVA with Sidak’s multiple comparisons (GraphPad Prism version 9).

Techniques: Staining, Incubation