omnigrid micro automated microspotter Search Results


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Digilab Inc omnigrid micro automated microspotter
A) Single- and two-way combinations of 10 liver-inspired recombinant ECM proteins. Each circle represents a single protein (collagens 1 [C1], 3 [C3], 4 [C4], 5 [C5] decorin [DC], fibronectin [FN], hyaluronic acid [HA], laminin [LN], lumican [LC], and tenascin [TC]) and each grey line represents a two-way protein combination; a total of 55 compositions of ECM proteins were utilized in this study. B) Schematic of the experimental workflow, including: fabrication of microarrays using an automated <t>microspotter</t> to transfer pre-made ECM protein solutions to a polyacrylamide (PA) hydrogel of a tunable stiffness conjugated to a glass slide; seeding of PHHs that attach only to the ECM protein ‘islands’ and not to the PA gel; differential attachment of PHHs and expression of PHH markers on ECM islands as assessed via high-content imaging; plotting and statistical analysis of single cell imaging data across the various ECM conditions. C) Representative section of an ECM microarray demonstrating the differential attachment of PHHs to ECM islands of 450 µm diameter; nuclei are counterstained with DAPI and rhodamine-labeled dextran spots on microarrays are utilized for alignment. Scale bar = 500 µm. D) Representative islands of 4-color-stained PHHs on the microarrays of two different PA stiffnesses, 1 kPa and 25 kPa (Young’s moduli). Scale bars = 50 µm. E) Box plots showing the median number of cells per ECM island (center bar) along with the interquartile range on both microarray stiffnesses over 14 days of culture (each dot represents the mean cell number measured across islands of a specific ECM composition); mean distributions were compared across the stiffnesses using the Wilcoxon Test. **p<0.01 and ****p<0.0001. F) Heatmap of mean cell number across islands of single- (dashed line) and two-way combinations of the ECM proteins on the two stiffnesses after 14 days of culture. Similar heatmaps after 1 and 7 days of culture are shown in Figure S1A , Supporting Information . For panels E and F, data displayed represents summarized single-cell measurements across three PHH donors per condition (n = 22–24 ECM islands across representative microarrays).
Omnigrid Micro Automated Microspotter, supplied by Digilab Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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A) Single- and two-way combinations of 10 liver-inspired recombinant ECM proteins. Each circle represents a single protein (collagens 1 [C1], 3 [C3], 4 [C4], 5 [C5] decorin [DC], fibronectin [FN], hyaluronic acid [HA], laminin [LN], lumican [LC], and tenascin [TC]) and each grey line represents a two-way protein combination; a total of 55 compositions of ECM proteins were utilized in this study. B) Schematic of the experimental workflow, including: fabrication of microarrays using an automated microspotter to transfer pre-made ECM protein solutions to a polyacrylamide (PA) hydrogel of a tunable stiffness conjugated to a glass slide; seeding of PHHs that attach only to the ECM protein ‘islands’ and not to the PA gel; differential attachment of PHHs and expression of PHH markers on ECM islands as assessed via high-content imaging; plotting and statistical analysis of single cell imaging data across the various ECM conditions. C) Representative section of an ECM microarray demonstrating the differential attachment of PHHs to ECM islands of 450 µm diameter; nuclei are counterstained with DAPI and rhodamine-labeled dextran spots on microarrays are utilized for alignment. Scale bar = 500 µm. D) Representative islands of 4-color-stained PHHs on the microarrays of two different PA stiffnesses, 1 kPa and 25 kPa (Young’s moduli). Scale bars = 50 µm. E) Box plots showing the median number of cells per ECM island (center bar) along with the interquartile range on both microarray stiffnesses over 14 days of culture (each dot represents the mean cell number measured across islands of a specific ECM composition); mean distributions were compared across the stiffnesses using the Wilcoxon Test. **p<0.01 and ****p<0.0001. F) Heatmap of mean cell number across islands of single- (dashed line) and two-way combinations of the ECM proteins on the two stiffnesses after 14 days of culture. Similar heatmaps after 1 and 7 days of culture are shown in Figure S1A , Supporting Information . For panels E and F, data displayed represents summarized single-cell measurements across three PHH donors per condition (n = 22–24 ECM islands across representative microarrays).

Journal: Advanced materials interfaces

Article Title: Elucidating Extracellular Matrix and Stiffness Control of Primary Human Hepatocyte Phenotype Via Cell Microarrays

doi: 10.1002/admi.202101284

Figure Lengend Snippet: A) Single- and two-way combinations of 10 liver-inspired recombinant ECM proteins. Each circle represents a single protein (collagens 1 [C1], 3 [C3], 4 [C4], 5 [C5] decorin [DC], fibronectin [FN], hyaluronic acid [HA], laminin [LN], lumican [LC], and tenascin [TC]) and each grey line represents a two-way protein combination; a total of 55 compositions of ECM proteins were utilized in this study. B) Schematic of the experimental workflow, including: fabrication of microarrays using an automated microspotter to transfer pre-made ECM protein solutions to a polyacrylamide (PA) hydrogel of a tunable stiffness conjugated to a glass slide; seeding of PHHs that attach only to the ECM protein ‘islands’ and not to the PA gel; differential attachment of PHHs and expression of PHH markers on ECM islands as assessed via high-content imaging; plotting and statistical analysis of single cell imaging data across the various ECM conditions. C) Representative section of an ECM microarray demonstrating the differential attachment of PHHs to ECM islands of 450 µm diameter; nuclei are counterstained with DAPI and rhodamine-labeled dextran spots on microarrays are utilized for alignment. Scale bar = 500 µm. D) Representative islands of 4-color-stained PHHs on the microarrays of two different PA stiffnesses, 1 kPa and 25 kPa (Young’s moduli). Scale bars = 50 µm. E) Box plots showing the median number of cells per ECM island (center bar) along with the interquartile range on both microarray stiffnesses over 14 days of culture (each dot represents the mean cell number measured across islands of a specific ECM composition); mean distributions were compared across the stiffnesses using the Wilcoxon Test. **p<0.01 and ****p<0.0001. F) Heatmap of mean cell number across islands of single- (dashed line) and two-way combinations of the ECM proteins on the two stiffnesses after 14 days of culture. Similar heatmaps after 1 and 7 days of culture are shown in Figure S1A , Supporting Information . For panels E and F, data displayed represents summarized single-cell measurements across three PHH donors per condition (n = 22–24 ECM islands across representative microarrays).

Article Snippet: Furthermore, an OmniGrid Micro automated microspotter (Digilab, MA) created array grids of 10 ECM proteins in one- and two-way combinations, for a total of 55 combinations ( Figure 1A ).

Techniques: High Throughput Screening Assay, Recombinant, Expressing, Imaging, Single Cell, Microarray, Labeling, Staining