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hyperion imaging system  (fluidigm)


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    Structured Review

    fluidigm hyperion imaging system
    Hyperion Imaging System, supplied by fluidigm, used in various techniques. Bioz Stars score: 93/100, based on 1523 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/hyperion imaging system/product/fluidigm
    Average 93 stars, based on 1523 article reviews
    hyperion imaging system - by Bioz Stars, 2026-05
    93/100 stars

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    fluidigm hyperion imaging mass cytometry system
    A. Dot plot of Gene set enrichment analyses (GSEA) from differentially expressed genes in basal cells of E14.5 versus E15.5/E16.5 embryos from scRNAseq data. B, C. Representative images (B) and quantification (C) of tissue sections from E14.5-16.5 embryos analyzed by mass <t>cytometry.</t> Note increased expression of basement membrane Collagen IV (counterstained with K10) and integrins α6 and β1 (mean ±SD; scale bars 50 µm; n=3 embryos/stage; Two-way ANOVA/Tukey’s (Left and middle panel), Kruskal-Wallis/Dunn’s (right panel)). D. Basement membrane Young’s moduli extracted from AFM force indentation experiments (Tukey’s box and whiskers; n>200 force curves pooled across 3embryos/stage; Kolmogorov-Smirnov). E. Representative images and quantification of skin wholemounts from E14.5 and E15.5 embryos stained for pMLC2 and phalloidin. Note increased pMLC2 intensity at cell junctions and interface between basal and suprabasal layers (arrows) (min-max box and whiskers; scale bars 10 µm; n=5 embryos/stage; Mann-Whitney) . F. Representative snapshots from live imaging movies and subsequent PIV analyses of velocity magnitudes of E14.5 and E15.5 epidermis from membrane-Tomato (mTomato) reporter mice. Red masks mark excluded hair follicle areas (scale bars 50 µm). G. Quantification of 2D cell perimeter, area and circularity from data in (A) (Tukey’s box and whiskers; n>2300 cells pooled across 3 embryos/stage; Mann-Whitney). H. Quantification of cell densities from data in (A) (mean ±SD; n=4 embryos/stage; Mann-Whitney). I. Quantification of velocity magnitudes from data in (A). Note attenuated velocity at E15.5 (mean ±SD; n=4 embryos/stage; Linear Mixed-Effects model.
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    A. Dot plot of Gene set enrichment analyses (GSEA) from differentially expressed genes in basal cells of E14.5 versus E15.5/E16.5 embryos from scRNAseq data. B, C. Representative images (B) and quantification (C) of tissue sections from E14.5-16.5 embryos analyzed by mass <t>cytometry.</t> Note increased expression of basement membrane Collagen IV (counterstained with K10) and integrins α6 and β1 (mean ±SD; scale bars 50 µm; n=3 embryos/stage; Two-way ANOVA/Tukey’s (Left and middle panel), Kruskal-Wallis/Dunn’s (right panel)). D. Basement membrane Young’s moduli extracted from AFM force indentation experiments (Tukey’s box and whiskers; n>200 force curves pooled across 3embryos/stage; Kolmogorov-Smirnov). E. Representative images and quantification of skin wholemounts from E14.5 and E15.5 embryos stained for pMLC2 and phalloidin. Note increased pMLC2 intensity at cell junctions and interface between basal and suprabasal layers (arrows) (min-max box and whiskers; scale bars 10 µm; n=5 embryos/stage; Mann-Whitney) . F. Representative snapshots from live imaging movies and subsequent PIV analyses of velocity magnitudes of E14.5 and E15.5 epidermis from membrane-Tomato (mTomato) reporter mice. Red masks mark excluded hair follicle areas (scale bars 50 µm). G. Quantification of 2D cell perimeter, area and circularity from data in (A) (Tukey’s box and whiskers; n>2300 cells pooled across 3 embryos/stage; Mann-Whitney). H. Quantification of cell densities from data in (A) (mean ±SD; n=4 embryos/stage; Mann-Whitney). I. Quantification of velocity magnitudes from data in (A). Note attenuated velocity at E15.5 (mean ±SD; n=4 embryos/stage; Linear Mixed-Effects model.
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    fluidigm hyperiontm imaging system
    A. Dot plot of Gene set enrichment analyses (GSEA) from differentially expressed genes in basal cells of E14.5 versus E15.5/E16.5 embryos from scRNAseq data. B, C. Representative images (B) and quantification (C) of tissue sections from E14.5-16.5 embryos analyzed by mass <t>cytometry.</t> Note increased expression of basement membrane Collagen IV (counterstained with K10) and integrins α6 and β1 (mean ±SD; scale bars 50 µm; n=3 embryos/stage; Two-way ANOVA/Tukey’s (Left and middle panel), Kruskal-Wallis/Dunn’s (right panel)). D. Basement membrane Young’s moduli extracted from AFM force indentation experiments (Tukey’s box and whiskers; n>200 force curves pooled across 3embryos/stage; Kolmogorov-Smirnov). E. Representative images and quantification of skin wholemounts from E14.5 and E15.5 embryos stained for pMLC2 and phalloidin. Note increased pMLC2 intensity at cell junctions and interface between basal and suprabasal layers (arrows) (min-max box and whiskers; scale bars 10 µm; n=5 embryos/stage; Mann-Whitney) . F. Representative snapshots from live imaging movies and subsequent PIV analyses of velocity magnitudes of E14.5 and E15.5 epidermis from membrane-Tomato (mTomato) reporter mice. Red masks mark excluded hair follicle areas (scale bars 50 µm). G. Quantification of 2D cell perimeter, area and circularity from data in (A) (Tukey’s box and whiskers; n>2300 cells pooled across 3 embryos/stage; Mann-Whitney). H. Quantification of cell densities from data in (A) (mean ±SD; n=4 embryos/stage; Mann-Whitney). I. Quantification of velocity magnitudes from data in (A). Note attenuated velocity at E15.5 (mean ±SD; n=4 embryos/stage; Linear Mixed-Effects model.
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    Bruker Corporation hyperion 3000 infrared microscope
    A. Dot plot of Gene set enrichment analyses (GSEA) from differentially expressed genes in basal cells of E14.5 versus E15.5/E16.5 embryos from scRNAseq data. B, C. Representative images (B) and quantification (C) of tissue sections from E14.5-16.5 embryos analyzed by mass <t>cytometry.</t> Note increased expression of basement membrane Collagen IV (counterstained with K10) and integrins α6 and β1 (mean ±SD; scale bars 50 µm; n=3 embryos/stage; Two-way ANOVA/Tukey’s (Left and middle panel), Kruskal-Wallis/Dunn’s (right panel)). D. Basement membrane Young’s moduli extracted from AFM force indentation experiments (Tukey’s box and whiskers; n>200 force curves pooled across 3embryos/stage; Kolmogorov-Smirnov). E. Representative images and quantification of skin wholemounts from E14.5 and E15.5 embryos stained for pMLC2 and phalloidin. Note increased pMLC2 intensity at cell junctions and interface between basal and suprabasal layers (arrows) (min-max box and whiskers; scale bars 10 µm; n=5 embryos/stage; Mann-Whitney) . F. Representative snapshots from live imaging movies and subsequent PIV analyses of velocity magnitudes of E14.5 and E15.5 epidermis from membrane-Tomato (mTomato) reporter mice. Red masks mark excluded hair follicle areas (scale bars 50 µm). G. Quantification of 2D cell perimeter, area and circularity from data in (A) (Tukey’s box and whiskers; n>2300 cells pooled across 3 embryos/stage; Mann-Whitney). H. Quantification of cell densities from data in (A) (mean ±SD; n=4 embryos/stage; Mann-Whitney). I. Quantification of velocity magnitudes from data in (A). Note attenuated velocity at E15.5 (mean ±SD; n=4 embryos/stage; Linear Mixed-Effects model.
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    Image Search Results


    A. Dot plot of Gene set enrichment analyses (GSEA) from differentially expressed genes in basal cells of E14.5 versus E15.5/E16.5 embryos from scRNAseq data. B, C. Representative images (B) and quantification (C) of tissue sections from E14.5-16.5 embryos analyzed by mass cytometry. Note increased expression of basement membrane Collagen IV (counterstained with K10) and integrins α6 and β1 (mean ±SD; scale bars 50 µm; n=3 embryos/stage; Two-way ANOVA/Tukey’s (Left and middle panel), Kruskal-Wallis/Dunn’s (right panel)). D. Basement membrane Young’s moduli extracted from AFM force indentation experiments (Tukey’s box and whiskers; n>200 force curves pooled across 3embryos/stage; Kolmogorov-Smirnov). E. Representative images and quantification of skin wholemounts from E14.5 and E15.5 embryos stained for pMLC2 and phalloidin. Note increased pMLC2 intensity at cell junctions and interface between basal and suprabasal layers (arrows) (min-max box and whiskers; scale bars 10 µm; n=5 embryos/stage; Mann-Whitney) . F. Representative snapshots from live imaging movies and subsequent PIV analyses of velocity magnitudes of E14.5 and E15.5 epidermis from membrane-Tomato (mTomato) reporter mice. Red masks mark excluded hair follicle areas (scale bars 50 µm). G. Quantification of 2D cell perimeter, area and circularity from data in (A) (Tukey’s box and whiskers; n>2300 cells pooled across 3 embryos/stage; Mann-Whitney). H. Quantification of cell densities from data in (A) (mean ±SD; n=4 embryos/stage; Mann-Whitney). I. Quantification of velocity magnitudes from data in (A). Note attenuated velocity at E15.5 (mean ±SD; n=4 embryos/stage; Linear Mixed-Effects model.

    Journal: bioRxiv

    Article Title: Tissue-scale mechanics controls differentiation strategy and dynamics of epithelial multilayering

    doi: 10.64898/2026.02.08.704529

    Figure Lengend Snippet: A. Dot plot of Gene set enrichment analyses (GSEA) from differentially expressed genes in basal cells of E14.5 versus E15.5/E16.5 embryos from scRNAseq data. B, C. Representative images (B) and quantification (C) of tissue sections from E14.5-16.5 embryos analyzed by mass cytometry. Note increased expression of basement membrane Collagen IV (counterstained with K10) and integrins α6 and β1 (mean ±SD; scale bars 50 µm; n=3 embryos/stage; Two-way ANOVA/Tukey’s (Left and middle panel), Kruskal-Wallis/Dunn’s (right panel)). D. Basement membrane Young’s moduli extracted from AFM force indentation experiments (Tukey’s box and whiskers; n>200 force curves pooled across 3embryos/stage; Kolmogorov-Smirnov). E. Representative images and quantification of skin wholemounts from E14.5 and E15.5 embryos stained for pMLC2 and phalloidin. Note increased pMLC2 intensity at cell junctions and interface between basal and suprabasal layers (arrows) (min-max box and whiskers; scale bars 10 µm; n=5 embryos/stage; Mann-Whitney) . F. Representative snapshots from live imaging movies and subsequent PIV analyses of velocity magnitudes of E14.5 and E15.5 epidermis from membrane-Tomato (mTomato) reporter mice. Red masks mark excluded hair follicle areas (scale bars 50 µm). G. Quantification of 2D cell perimeter, area and circularity from data in (A) (Tukey’s box and whiskers; n>2300 cells pooled across 3 embryos/stage; Mann-Whitney). H. Quantification of cell densities from data in (A) (mean ±SD; n=4 embryos/stage; Mann-Whitney). I. Quantification of velocity magnitudes from data in (A). Note attenuated velocity at E15.5 (mean ±SD; n=4 embryos/stage; Linear Mixed-Effects model.

    Article Snippet: The samples were laser-ablated at 200 Hz using a Hyperion imaging mass cytometry system (Fluidigm) coupled to a Helios time-of-flight mass cytometer with a resolution of 1 μm.

    Techniques: Mass Cytometry, Expressing, Membrane, Staining, MANN-WHITNEY, Imaging

    A. Representative images and quantifications of tissue sections from E14.5-16.5 embryos analyzed by mass cytometry. Note increased expression of integrin β4 (mean ±SD; scale bars 50 µm; n=3 embryos/stage; Two-way ANOVA/Tukey’s.

    Journal: bioRxiv

    Article Title: Tissue-scale mechanics controls differentiation strategy and dynamics of epithelial multilayering

    doi: 10.64898/2026.02.08.704529

    Figure Lengend Snippet: A. Representative images and quantifications of tissue sections from E14.5-16.5 embryos analyzed by mass cytometry. Note increased expression of integrin β4 (mean ±SD; scale bars 50 µm; n=3 embryos/stage; Two-way ANOVA/Tukey’s.

    Article Snippet: The samples were laser-ablated at 200 Hz using a Hyperion imaging mass cytometry system (Fluidigm) coupled to a Helios time-of-flight mass cytometer with a resolution of 1 μm.

    Techniques: Mass Cytometry, Expressing