parametric unpaired multiple t tests Search Results


multiple t-test or unpaired t-test or one-way anova or two-way anova  (GraphPad Software Inc)
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GraphPad Software Inc multiple t-test or unpaired t-test or one-way anova or two-way anova
SNI activates the morphological transformation of microglia into amoeba-like cells. ( A ) Representative immunofluorescence staining image of Iba1-IR (microglial marker, magenta) in the bilateral ACC of sham and SNI groups. Scale bar = 50 μm. ( B ) Comparison of the process lengths and cell body areas of microglia in the bilateral ACC of sham and SNI groups. * p -value < 0.05, ** p -value < 0.01, *** p -value < 0.001 versus the sham <t>group</t> <t>(unpaired</t> t test). ( C ) Left: representative immunofluorescence staining image showing CD68-IR in the bilateral ACC in both sham and SNI rats. Scale bar = 50 μm. Right: quantification of the CD68 fluorescence signals in both groups. ** p -value < 0.01 versus the sham group (two-way <t>ANOVA).</t> ( D ) White arrow heads indicate the co-localization of CD68-IR (red) with that of vGAT (green, top) and PV (green, below) 7d post SNI by double staining. Scale bar = 25 μm in the top line; 50 μm in the bottom line. Blue fluorescence in (A, C and D) is from DAPI, a nuclear counterstain.
Multiple T Test Or Unpaired T Test Or One Way Anova Or Two Way Anova, 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
multiple t-test or unpaired t-test or one-way anova or two-way anova - by Bioz Stars, 2026-03
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parametric unpaired multiple t tests  (GraphPad Software Inc)
90
GraphPad Software Inc parametric unpaired multiple t tests
SNI activates the morphological transformation of microglia into amoeba-like cells. ( A ) Representative immunofluorescence staining image of Iba1-IR (microglial marker, magenta) in the bilateral ACC of sham and SNI groups. Scale bar = 50 μm. ( B ) Comparison of the process lengths and cell body areas of microglia in the bilateral ACC of sham and SNI groups. * p -value < 0.05, ** p -value < 0.01, *** p -value < 0.001 versus the sham <t>group</t> <t>(unpaired</t> t test). ( C ) Left: representative immunofluorescence staining image showing CD68-IR in the bilateral ACC in both sham and SNI rats. Scale bar = 50 μm. Right: quantification of the CD68 fluorescence signals in both groups. ** p -value < 0.01 versus the sham group (two-way <t>ANOVA).</t> ( D ) White arrow heads indicate the co-localization of CD68-IR (red) with that of vGAT (green, top) and PV (green, below) 7d post SNI by double staining. Scale bar = 25 μm in the top line; 50 μm in the bottom line. Blue fluorescence in (A, C and D) is from DAPI, a nuclear counterstain.
Parametric Unpaired Multiple T Tests, 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/result/parametric unpaired multiple t tests/product/GraphPad Software Inc
Average 90 stars, based on 1 article reviews
parametric unpaired multiple t tests - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
unpaired multiple t test analysis of timepoints 12 h and 48 h using graphpad prism 8.4.3  (GraphPad Software Inc)
90
GraphPad Software Inc unpaired multiple t test analysis of timepoints 12 h and 48 h using graphpad prism 8.4.3
SNI activates the morphological transformation of microglia into amoeba-like cells. ( A ) Representative immunofluorescence staining image of Iba1-IR (microglial marker, magenta) in the bilateral ACC of sham and SNI groups. Scale bar = 50 μm. ( B ) Comparison of the process lengths and cell body areas of microglia in the bilateral ACC of sham and SNI groups. * p -value < 0.05, ** p -value < 0.01, *** p -value < 0.001 versus the sham <t>group</t> <t>(unpaired</t> t test). ( C ) Left: representative immunofluorescence staining image showing CD68-IR in the bilateral ACC in both sham and SNI rats. Scale bar = 50 μm. Right: quantification of the CD68 fluorescence signals in both groups. ** p -value < 0.01 versus the sham group (two-way <t>ANOVA).</t> ( D ) White arrow heads indicate the co-localization of CD68-IR (red) with that of vGAT (green, top) and PV (green, below) 7d post SNI by double staining. Scale bar = 25 μm in the top line; 50 μm in the bottom line. Blue fluorescence in (A, C and D) is from DAPI, a nuclear counterstain.
Unpaired Multiple T Test Analysis Of Timepoints 12 H And 48 H Using Graphpad Prism 8.4.3, 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/result/unpaired multiple t test analysis of timepoints 12 h and 48 h using graphpad prism 8.4.3/product/GraphPad Software Inc
Average 90 stars, based on 1 article reviews
unpaired multiple t test analysis of timepoints 12 h and 48 h using graphpad prism 8.4.3 - by Bioz Stars, 2026-03
90/100 stars
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Image Search Results


SNI activates the morphological transformation of microglia into amoeba-like cells. ( A ) Representative immunofluorescence staining image of Iba1-IR (microglial marker, magenta) in the bilateral ACC of sham and SNI groups. Scale bar = 50 μm. ( B ) Comparison of the process lengths and cell body areas of microglia in the bilateral ACC of sham and SNI groups. * p -value < 0.05, ** p -value < 0.01, *** p -value < 0.001 versus the sham group (unpaired t test). ( C ) Left: representative immunofluorescence staining image showing CD68-IR in the bilateral ACC in both sham and SNI rats. Scale bar = 50 μm. Right: quantification of the CD68 fluorescence signals in both groups. ** p -value < 0.01 versus the sham group (two-way ANOVA). ( D ) White arrow heads indicate the co-localization of CD68-IR (red) with that of vGAT (green, top) and PV (green, below) 7d post SNI by double staining. Scale bar = 25 μm in the top line; 50 μm in the bottom line. Blue fluorescence in (A, C and D) is from DAPI, a nuclear counterstain.

Journal: International Journal of Molecular Sciences

Article Title: NLRP3-Mediated Piezo1 Upregulation in ACC Inhibitory Parvalbumin-Expressing Interneurons Is Involved in Pain Processing after Peripheral Nerve Injury

doi: 10.3390/ijms232113035

Figure Lengend Snippet: SNI activates the morphological transformation of microglia into amoeba-like cells. ( A ) Representative immunofluorescence staining image of Iba1-IR (microglial marker, magenta) in the bilateral ACC of sham and SNI groups. Scale bar = 50 μm. ( B ) Comparison of the process lengths and cell body areas of microglia in the bilateral ACC of sham and SNI groups. * p -value < 0.05, ** p -value < 0.01, *** p -value < 0.001 versus the sham group (unpaired t test). ( C ) Left: representative immunofluorescence staining image showing CD68-IR in the bilateral ACC in both sham and SNI rats. Scale bar = 50 μm. Right: quantification of the CD68 fluorescence signals in both groups. ** p -value < 0.01 versus the sham group (two-way ANOVA). ( D ) White arrow heads indicate the co-localization of CD68-IR (red) with that of vGAT (green, top) and PV (green, below) 7d post SNI by double staining. Scale bar = 25 μm in the top line; 50 μm in the bottom line. Blue fluorescence in (A, C and D) is from DAPI, a nuclear counterstain.

Article Snippet: GraphPad Software was used for multiple t -test or unpaired t -test or one-way ANOVA or two-way ANOVA to determine the differences over different groups where appropriate.

Techniques: Transformation Assay, Immunofluorescence, Staining, Marker, Comparison, Fluorescence, Double Staining