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microarray spotter (omnigrid micro  (Digilab Inc)

 
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    Structured Review

    Digilab Inc microarray spotter (omnigrid micro
    ( A ) Correlation of fluorescence intensities of spots obtained after FUN 1 staining with the number of viable cells present in each spot. The fluorescence intensities were measured using a <t>microarray</t> scanner and the values are expressed as RFUs. ( B ) Fluorescence intensity of nano-biofilms on Ca BChip stained with FUN 1. Values represent mean and standard deviations of multiple independent biofilms formed in each of 9 different blocks of the chip.
    Microarray Spotter (Omnigrid Micro, supplied by Digilab 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/microarray spotter (omnigrid micro/product/Digilab Inc
    Average 90 stars, based on 1 article reviews
    microarray spotter (omnigrid micro - by Bioz Stars, 2026-05
    90/100 stars

    Images

    1) Product Images from "Development of a High-Throughput Candida albicans Biofilm Chip"

    Article Title: Development of a High-Throughput Candida albicans Biofilm Chip

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0019036

    ( A ) Correlation of fluorescence intensities of spots obtained after FUN 1 staining with the number of viable cells present in each spot. The fluorescence intensities were measured using a microarray scanner and the values are expressed as RFUs. ( B ) Fluorescence intensity of nano-biofilms on Ca BChip stained with FUN 1. Values represent mean and standard deviations of multiple independent biofilms formed in each of 9 different blocks of the chip.
    Figure Legend Snippet: ( A ) Correlation of fluorescence intensities of spots obtained after FUN 1 staining with the number of viable cells present in each spot. The fluorescence intensities were measured using a microarray scanner and the values are expressed as RFUs. ( B ) Fluorescence intensity of nano-biofilms on Ca BChip stained with FUN 1. Values represent mean and standard deviations of multiple independent biofilms formed in each of 9 different blocks of the chip.

    Techniques Used: Fluorescence, Staining, Microarray

    ( A ) Schematic of attachment of collagen-encapsulated C. albicans biofilms to modified glass slides. Glass slides modified with APTES were coated with PSMA and a suspension of C. albicans yeast cells in microbiological media and collagen as encapsulating material was spotted onto the glass slides. ( B ) The optimal concentrations of growth media, inocula, collagen and PSMA that supported maximum biofilm yield in spots that also attached robustly to substrate were obtained from a factorial design study. ( C ) A picture of the high-thoughput Ca BChip, printed using a robotic microarrayer and containing 768 spots on PSMA-coated slides. Each hemispherical spot is 50 nL in volume, approximately 700 µm in diameter, and with a 1.2 mm separation between spots. Also shown is a fluorescent picture of fungal biofilms formed on the chip and stained with FUN 1, taken with a microarray scanner, alongside a close-up image of nano-biofilms.
    Figure Legend Snippet: ( A ) Schematic of attachment of collagen-encapsulated C. albicans biofilms to modified glass slides. Glass slides modified with APTES were coated with PSMA and a suspension of C. albicans yeast cells in microbiological media and collagen as encapsulating material was spotted onto the glass slides. ( B ) The optimal concentrations of growth media, inocula, collagen and PSMA that supported maximum biofilm yield in spots that also attached robustly to substrate were obtained from a factorial design study. ( C ) A picture of the high-thoughput Ca BChip, printed using a robotic microarrayer and containing 768 spots on PSMA-coated slides. Each hemispherical spot is 50 nL in volume, approximately 700 µm in diameter, and with a 1.2 mm separation between spots. Also shown is a fluorescent picture of fungal biofilms formed on the chip and stained with FUN 1, taken with a microarray scanner, alongside a close-up image of nano-biofilms.

    Techniques Used: Modification, Staining, Microarray

    ( A ) Light microscopy: a series of microphotographs showing the formation of nano-biofilms over time upon incubation at 37°C after initial printing using the robotic microarrayer. Magnification is ×100 for all panels. ( B ) Growth kinetics of C. albicans biofilm formation in Ca BChip as determined using FUN 1 staining and a microarray reader. Cells were printed on the chips, incubated at 37°C and fluorescence readings were taken over a 48 hour period. Results are expressed as arbitrary Relative Fluorescence Units (RFUs).
    Figure Legend Snippet: ( A ) Light microscopy: a series of microphotographs showing the formation of nano-biofilms over time upon incubation at 37°C after initial printing using the robotic microarrayer. Magnification is ×100 for all panels. ( B ) Growth kinetics of C. albicans biofilm formation in Ca BChip as determined using FUN 1 staining and a microarray reader. Cells were printed on the chips, incubated at 37°C and fluorescence readings were taken over a 48 hour period. Results are expressed as arbitrary Relative Fluorescence Units (RFUs).

    Techniques Used: Light Microscopy, Incubation, Staining, Microarray, Fluorescence



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    ( A ) Correlation of fluorescence intensities of spots obtained after FUN 1 staining with the number of viable cells present in each spot. The fluorescence intensities were measured using a <t>microarray</t> scanner and the values are expressed as RFUs. ( B ) Fluorescence intensity of nano-biofilms on Ca BChip stained with FUN 1. Values represent mean and standard deviations of multiple independent biofilms formed in each of 9 different blocks of the chip.
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    ( A ) Correlation of fluorescence intensities of spots obtained after FUN 1 staining with the number of viable cells present in each spot. The fluorescence intensities were measured using a <t>microarray</t> scanner and the values are expressed as RFUs. ( B ) Fluorescence intensity of nano-biofilms on Ca BChip stained with FUN 1. Values represent mean and standard deviations of multiple independent biofilms formed in each of 9 different blocks of the chip.
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    microarray spotter omnigrid micro  (Digilab Inc)
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    ( A ) Correlation of fluorescence intensities of spots obtained after FUN 1 staining with the number of viable cells present in each spot. The fluorescence intensities were measured using a <t>microarray</t> scanner and the values are expressed as RFUs. ( B ) Fluorescence intensity of nano-biofilms on Ca BChip stained with FUN 1. Values represent mean and standard deviations of multiple independent biofilms formed in each of 9 different blocks of the chip.
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    https://www.bioz.com/result/microarray spotter omnigrid micro/product/Digilab Inc
    Average 90 stars, based on 1 article reviews
    microarray spotter omnigrid micro - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    ( A ) Correlation of fluorescence intensities of spots obtained after FUN 1 staining with the number of viable cells present in each spot. The fluorescence intensities were measured using a microarray scanner and the values are expressed as RFUs. ( B ) Fluorescence intensity of nano-biofilms on Ca BChip stained with FUN 1. Values represent mean and standard deviations of multiple independent biofilms formed in each of 9 different blocks of the chip.

    Journal: PLoS ONE

    Article Title: Development of a High-Throughput Candida albicans Biofilm Chip

    doi: 10.1371/journal.pone.0019036

    Figure Lengend Snippet: ( A ) Correlation of fluorescence intensities of spots obtained after FUN 1 staining with the number of viable cells present in each spot. The fluorescence intensities were measured using a microarray scanner and the values are expressed as RFUs. ( B ) Fluorescence intensity of nano-biofilms on Ca BChip stained with FUN 1. Values represent mean and standard deviations of multiple independent biofilms formed in each of 9 different blocks of the chip.

    Article Snippet: The suspension containing yeast cells, collagen and media was printed (50 nL per spot) on the functionalized PSMA-coated glass slides using a microarray spotter (Omnigrid Micro, Digilab Inc., Holliston, MA).

    Techniques: Fluorescence, Staining, Microarray

    ( A ) Schematic of attachment of collagen-encapsulated C. albicans biofilms to modified glass slides. Glass slides modified with APTES were coated with PSMA and a suspension of C. albicans yeast cells in microbiological media and collagen as encapsulating material was spotted onto the glass slides. ( B ) The optimal concentrations of growth media, inocula, collagen and PSMA that supported maximum biofilm yield in spots that also attached robustly to substrate were obtained from a factorial design study. ( C ) A picture of the high-thoughput Ca BChip, printed using a robotic microarrayer and containing 768 spots on PSMA-coated slides. Each hemispherical spot is 50 nL in volume, approximately 700 µm in diameter, and with a 1.2 mm separation between spots. Also shown is a fluorescent picture of fungal biofilms formed on the chip and stained with FUN 1, taken with a microarray scanner, alongside a close-up image of nano-biofilms.

    Journal: PLoS ONE

    Article Title: Development of a High-Throughput Candida albicans Biofilm Chip

    doi: 10.1371/journal.pone.0019036

    Figure Lengend Snippet: ( A ) Schematic of attachment of collagen-encapsulated C. albicans biofilms to modified glass slides. Glass slides modified with APTES were coated with PSMA and a suspension of C. albicans yeast cells in microbiological media and collagen as encapsulating material was spotted onto the glass slides. ( B ) The optimal concentrations of growth media, inocula, collagen and PSMA that supported maximum biofilm yield in spots that also attached robustly to substrate were obtained from a factorial design study. ( C ) A picture of the high-thoughput Ca BChip, printed using a robotic microarrayer and containing 768 spots on PSMA-coated slides. Each hemispherical spot is 50 nL in volume, approximately 700 µm in diameter, and with a 1.2 mm separation between spots. Also shown is a fluorescent picture of fungal biofilms formed on the chip and stained with FUN 1, taken with a microarray scanner, alongside a close-up image of nano-biofilms.

    Article Snippet: The suspension containing yeast cells, collagen and media was printed (50 nL per spot) on the functionalized PSMA-coated glass slides using a microarray spotter (Omnigrid Micro, Digilab Inc., Holliston, MA).

    Techniques: Modification, Staining, Microarray

    ( A ) Light microscopy: a series of microphotographs showing the formation of nano-biofilms over time upon incubation at 37°C after initial printing using the robotic microarrayer. Magnification is ×100 for all panels. ( B ) Growth kinetics of C. albicans biofilm formation in Ca BChip as determined using FUN 1 staining and a microarray reader. Cells were printed on the chips, incubated at 37°C and fluorescence readings were taken over a 48 hour period. Results are expressed as arbitrary Relative Fluorescence Units (RFUs).

    Journal: PLoS ONE

    Article Title: Development of a High-Throughput Candida albicans Biofilm Chip

    doi: 10.1371/journal.pone.0019036

    Figure Lengend Snippet: ( A ) Light microscopy: a series of microphotographs showing the formation of nano-biofilms over time upon incubation at 37°C after initial printing using the robotic microarrayer. Magnification is ×100 for all panels. ( B ) Growth kinetics of C. albicans biofilm formation in Ca BChip as determined using FUN 1 staining and a microarray reader. Cells were printed on the chips, incubated at 37°C and fluorescence readings were taken over a 48 hour period. Results are expressed as arbitrary Relative Fluorescence Units (RFUs).

    Article Snippet: The suspension containing yeast cells, collagen and media was printed (50 nL per spot) on the functionalized PSMA-coated glass slides using a microarray spotter (Omnigrid Micro, Digilab Inc., Holliston, MA).

    Techniques: Light Microscopy, Incubation, Staining, Microarray, Fluorescence