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2d maximum intensity projection images  (Softworx Inc)

 
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    Softworx Inc 2d maximum intensity projection images
    2d Maximum Intensity Projection Images, supplied by Softworx 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/intensity+projection/bio_rxiv__64898__2026__01__30__702603-390-0-7?v=Softworx+Inc
    Average 86 stars, based on 1 article reviews
    2d maximum intensity projection images - by Bioz Stars, 2026-08
    86/100 stars

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    IPNs can be formed and dynamically softened in a cytocompatible manner. (a) Experimental set-up for viability measurements. Static controls of thiol-ene, IPN, and SPAAC gels were compared against dynamic IPN gels treated with 4S9 on day 3 of culture. (b) Maximum Image Projection <t>(MIP)</t> of representative images (z = 250 μm). Live/Dead staining <t>of</t> <t>encapsulated</t> 10T1/2 fibroblasts shows excellent cytocompatibility of all possible network types on day 7 of culture. Scale bar = 100 μm. (c) Quantification of viability.
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    Each Z -stack in the time-series is converted to a single image by a <t>MIP</t> 2D projection <t>in</t> <t>Imaris.</t> Then the time-series is imported into Matlab and the projected area of each cell is found by an edge detection algorithm. The time series shows a single cell with the edge marked in red at different time points, t 1, t 2, and t 3. Note that, for simplicity, only one cell is shown; however, there are more cells within the FOV.
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    Each Z -stack in the time-series is converted to a single image by a <t>MIP</t> 2D projection <t>in</t> <t>Imaris.</t> Then the time-series is imported into Matlab and the projected area of each cell is found by an edge detection algorithm. The time series shows a single cell with the edge marked in red at different time points, t 1, t 2, and t 3. Note that, for simplicity, only one cell is shown; however, there are more cells within the FOV.
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    Image Search Results


    IPNs can be formed and dynamically softened in a cytocompatible manner. (a) Experimental set-up for viability measurements. Static controls of thiol-ene, IPN, and SPAAC gels were compared against dynamic IPN gels treated with 4S9 on day 3 of culture. (b) Maximum Image Projection (MIP) of representative images (z = 250 μm). Live/Dead staining of encapsulated 10T1/2 fibroblasts shows excellent cytocompatibility of all possible network types on day 7 of culture. Scale bar = 100 μm. (c) Quantification of viability.

    Journal: Advanced materials (Deerfield Beach, Fla.)

    Article Title: Stepwise Stiffening/Softening of and Cell Recovery from Reversibly Formulated Hydrogel Interpenetrating Networks

    doi: 10.1002/adma.202404880

    Figure Lengend Snippet: IPNs can be formed and dynamically softened in a cytocompatible manner. (a) Experimental set-up for viability measurements. Static controls of thiol-ene, IPN, and SPAAC gels were compared against dynamic IPN gels treated with 4S9 on day 3 of culture. (b) Maximum Image Projection (MIP) of representative images (z = 250 μm). Live/Dead staining of encapsulated 10T1/2 fibroblasts shows excellent cytocompatibility of all possible network types on day 7 of culture. Scale bar = 100 μm. (c) Quantification of viability.

    Article Snippet: Live/dead count was quantified from 250 μm max intensity projections (MIP) using IMARIS. hMSCs were encapsulated in gels at a concentration of 2 × 10 6 cells mL −1 and cultured for 7 days in either bulk or patterned gels.

    Techniques: Staining

    Each Z -stack in the time-series is converted to a single image by a MIP 2D projection in Imaris. Then the time-series is imported into Matlab and the projected area of each cell is found by an edge detection algorithm. The time series shows a single cell with the edge marked in red at different time points, t 1, t 2, and t 3. Note that, for simplicity, only one cell is shown; however, there are more cells within the FOV.

    Journal: Measurement Science & Technology

    Article Title: Viscoelastic recovery times of chondrocytes measured using a novel 3D-printed microfluidic device

    doi: 10.1088/1361-6501/adf65a

    Figure Lengend Snippet: Each Z -stack in the time-series is converted to a single image by a MIP 2D projection in Imaris. Then the time-series is imported into Matlab and the projected area of each cell is found by an edge detection algorithm. The time series shows a single cell with the edge marked in red at different time points, t 1, t 2, and t 3. Note that, for simplicity, only one cell is shown; however, there are more cells within the FOV.

    Article Snippet: To calculate the total projected area (shadow) of the cells before, during, and after compression, each Z -stack of the time series was reduced to a single image using the maximum intensity projection (MIP) operation in Imaris (Oxford Instruments).

    Techniques: