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tukey test in minitab  (Minitab Inc)

 
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    Minitab Inc tukey test in minitab
    Tukey Test In Minitab, supplied by Minitab Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tukey+tests/test+tukey/pm42070601-124-18-21
    Average 86 stars, based on 1 article reviews
    tukey test in minitab - by Bioz Stars, 2026-09
    86/100 stars

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    Article Title: Quantification of Reducing Sugars Based on the Qualitative Technique of Benedict
    Article Snippet: Tukey tests were performed to determine the significant differences between the corresponding absorbances of each of the copper concentrations using MINITAB (USA).

    Article Title: Particle size of Cymbopogon Nardus powder affect Geraniol extracted by Novel Extraction Method using hard cap Espresso Machine
    Article Snippet: Espresso machine is proven to be effective to extract compound from herbal plants in small scale.. Particle size is one of critical parameters affecting amount of bioactive compound extracted from the plants.. Therefore, in this study, a novel and economical pressurized liquid extraction method based on a hard caps espresso machine has been developed.

    Article Title: Trueness and stability of additively manufactured removable dies: An in vitro study on plant-based resins and alcohol-free cleaning solutions.
    Article Snippet: Fixed effects were tested using the Kenward-Roger approximation, and post hoc pairwise comparisons were performed with Tukey tests (Minitab v19; Minitab, LLC) (α=.05).

    Article Title: Well-Defined Morphology Enables Tuning of the Antimicrobial Activity of ZnO Nanoparticles
    Article Snippet: The results are presented as averages with standard deviations; statistical analysis was performed using ANOVA and Tukey tests at the 95% confidence level, with Minitab v 20 (Minitab LLC, State College, PA, USA).

    Article Title: Transmission-enhancing effects of a plant virus depend on host association with beneficial bacteria
    Article Snippet: Vector-borne viruses can alter host-plant chemistry and thereby influence interactions between plants and vectors, frequently in ways that enhance their own transmission.. However, these interactions may also be influenced by the presence of other symbiotic microorganisms, including co-evolved plant mutualists.. Here, we explore how rhizobia colonization influences plant virus effects on host chemistry, vector behavior, and virus transmission using a system consisting of Medicago truncatula, Alfalfa mosaic virus (AMV), its aphid vector Acyrthosiphon pisum, and the rhizobial symbiont Sinorhizobium.



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    Deletion of the gh18-10 ENGase increases Neurospora crassa tolerance to variable stress conditions. ( A ) Representative colony morphology of Neurospora crassa wild type (WT), Δ gh18-10 , and Δ pngA strain grown on solid VM medium under control conditions or supplemented with caffeine (cell wall stress), CoCl₂ (hypoxia), DTT (ER stress), H₂O₂ (oxidative stress), or tunicamycin (ER stress). ( B ) Mycelia growth was quantified as mycelial diameter (cm) under each condition (right) 24 hours post inoculation at 30°C. Bars represent the mean ± error. Asterisks indicate statistically significant differences relative to WT ( p < 0.05) according to <t>Tukey</t> <t>test.</t>
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    Deletion of the gh18-10 ENGase increases Neurospora crassa tolerance to variable stress conditions. ( A ) Representative colony morphology of Neurospora crassa wild type (WT), Δ gh18-10 , and Δ pngA strain grown on solid VM medium under control conditions or supplemented with caffeine (cell wall stress), CoCl₂ (hypoxia), DTT (ER stress), H₂O₂ (oxidative stress), or tunicamycin (ER stress). ( B ) Mycelia growth was quantified as mycelial diameter (cm) under each condition (right) 24 hours post inoculation at 30°C. Bars represent the mean ± error. Asterisks indicate statistically significant differences relative to WT ( p < 0.05) according to <t>Tukey</t> <t>test.</t>
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    Deletion of the gh18-10 ENGase increases Neurospora crassa tolerance to variable stress conditions. ( A ) Representative colony morphology of Neurospora crassa wild type (WT), Δ gh18-10 , and Δ pngA strain grown on solid VM medium under control conditions or supplemented with caffeine (cell wall stress), CoCl₂ (hypoxia), DTT (ER stress), H₂O₂ (oxidative stress), or tunicamycin (ER stress). ( B ) Mycelia growth was quantified as mycelial diameter (cm) under each condition (right) 24 hours post inoculation at 30°C. Bars represent the mean ± error. Asterisks indicate statistically significant differences relative to WT ( p < 0.05) according to <t>Tukey</t> <t>test.</t>
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    Deletion of the gh18-10 ENGase increases Neurospora crassa tolerance to variable stress conditions. ( A ) Representative colony morphology of Neurospora crassa wild type (WT), Δ gh18-10 , and Δ pngA strain grown on solid VM medium under control conditions or supplemented with caffeine (cell wall stress), CoCl₂ (hypoxia), DTT (ER stress), H₂O₂ (oxidative stress), or tunicamycin (ER stress). ( B ) Mycelia growth was quantified as mycelial diameter (cm) under each condition (right) 24 hours post inoculation at 30°C. Bars represent the mean ± error. Asterisks indicate statistically significant differences relative to WT ( p < 0.05) according to <t>Tukey</t> <t>test.</t>
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    Deletion of the gh18-10 ENGase increases Neurospora crassa tolerance to variable stress conditions. ( A ) Representative colony morphology of Neurospora crassa wild type (WT), Δ gh18-10 , and Δ pngA strain grown on solid VM medium under control conditions or supplemented with caffeine (cell wall stress), CoCl₂ (hypoxia), DTT (ER stress), H₂O₂ (oxidative stress), or tunicamycin (ER stress). ( B ) Mycelia growth was quantified as mycelial diameter (cm) under each condition (right) 24 hours post inoculation at 30°C. Bars represent the mean ± error. Asterisks indicate statistically significant differences relative to WT ( p < 0.05) according to Tukey test.

    Journal: bioRxiv

    Article Title: Functional and transcriptomic analyses in Neurospora crassa reveal the crucial role of N-glycoprotein deglycosylation process in fungal homeostasis

    doi: 10.64898/2026.03.25.714127

    Figure Lengend Snippet: Deletion of the gh18-10 ENGase increases Neurospora crassa tolerance to variable stress conditions. ( A ) Representative colony morphology of Neurospora crassa wild type (WT), Δ gh18-10 , and Δ pngA strain grown on solid VM medium under control conditions or supplemented with caffeine (cell wall stress), CoCl₂ (hypoxia), DTT (ER stress), H₂O₂ (oxidative stress), or tunicamycin (ER stress). ( B ) Mycelia growth was quantified as mycelial diameter (cm) under each condition (right) 24 hours post inoculation at 30°C. Bars represent the mean ± error. Asterisks indicate statistically significant differences relative to WT ( p < 0.05) according to Tukey test.

    Article Snippet: Statistical analysis was performed using one-way ANOVA using the Tukey test (p < 0.05) (Minitab, LLC, 2021).

    Techniques: Control

    The Neurospora crassa nag-1 gene coding for a putative GH20 N-acetyl hexosaminidase is uniquely induced on gh18-10 deletion strain upon ER stress. (A ) Venn diagram of differentially expressed genes (DEGs) of Δ pngA , Δ gh18-10 and WT strain grown under tunicamycin ER stress conditions. ( B ) Predicted schematic overview and structural comparison highlighting similarities between the nag-1 and gh18-10 enzymes. PDB structures were generated using AlphaFold 3, and structural alignments were performed with TM-align using default parameters. ( C ) Phenotypic analysis of nag-1 deletion strain under tunicamycin stress conditions. Mycelial radial growth was measured 24 h of incubation at 30 °C. Different letters (a, b, c) indicate statistically significant differences, and bars represent the mean ± error. Asterisks indicate statistically significant differences ( p < 0.05) according to Tukey test.

    Journal: bioRxiv

    Article Title: Functional and transcriptomic analyses in Neurospora crassa reveal the crucial role of N-glycoprotein deglycosylation process in fungal homeostasis

    doi: 10.64898/2026.03.25.714127

    Figure Lengend Snippet: The Neurospora crassa nag-1 gene coding for a putative GH20 N-acetyl hexosaminidase is uniquely induced on gh18-10 deletion strain upon ER stress. (A ) Venn diagram of differentially expressed genes (DEGs) of Δ pngA , Δ gh18-10 and WT strain grown under tunicamycin ER stress conditions. ( B ) Predicted schematic overview and structural comparison highlighting similarities between the nag-1 and gh18-10 enzymes. PDB structures were generated using AlphaFold 3, and structural alignments were performed with TM-align using default parameters. ( C ) Phenotypic analysis of nag-1 deletion strain under tunicamycin stress conditions. Mycelial radial growth was measured 24 h of incubation at 30 °C. Different letters (a, b, c) indicate statistically significant differences, and bars represent the mean ± error. Asterisks indicate statistically significant differences ( p < 0.05) according to Tukey test.

    Article Snippet: Statistical analysis was performed using one-way ANOVA using the Tukey test (p < 0.05) (Minitab, LLC, 2021).

    Techniques: Comparison, Generated, Incubation