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nikon nis elements software  (Nikon)


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    Nikon nikon nis elements software
    A. brasilense AR mutant exhibits elevated levels of intracellular c-di-GMP. Colony morphology of wild-type A. brasilense Sp7 ( A ) and the AR mutant ( B ) expressing a c-di-GMP biosensor (pFY4535). Cultures were grown for five days at 30 °C on Nfb∗ agar supplemented with KNO 3 . The intracellular c-di-GMP concentration is proportional to the expression of TurboRFP (red), resulting in a red colony color. The AR mutant's more intense coloration indicates higher c-di-GMP accumulation than in the WT. Representative fluorescence microscopy of individual WT and AR mutant cells. Images were captured on a Nikon Eclipse TE2000-U microscope using the following excitation/emission wavelengths: 489/519 nm for AmCyan (green) and 553/574 nm for TurboRFP (red). Gray images are intensity surface plots corresponding to the fluorescence emitted by TurboRFP. Images were processed using Nikon <t>NIS</t> <t>Elements</t> <t>software.</t> All images shown are representative of three independent experiments. Scale bars, 10 mm (colonies); 10 μm (individual cells). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Nikon Nis Elements Software, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 39515 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nikon+nis+elements+software/NIS-Elements/pmc12811640-111-7-7
    Average 99 stars, based on 39515 article reviews
    nikon nis elements software - by Bioz Stars, 2026-09
    99/100 stars

    Images

    1) Product Images from "Inactivation of Cysteine Synthase CysK-A enhances flocculation, biofilm formation, and sensitivity to oxidative stress in Azospirillum brasilense Sp7"

    Article Title: Inactivation of Cysteine Synthase CysK-A enhances flocculation, biofilm formation, and sensitivity to oxidative stress in Azospirillum brasilense Sp7

    Journal: Biofilm

    doi: 10.1016/j.bioflm.2025.100335

    A. brasilense AR mutant exhibits elevated levels of intracellular c-di-GMP. Colony morphology of wild-type A. brasilense Sp7 ( A ) and the AR mutant ( B ) expressing a c-di-GMP biosensor (pFY4535). Cultures were grown for five days at 30 °C on Nfb∗ agar supplemented with KNO 3 . The intracellular c-di-GMP concentration is proportional to the expression of TurboRFP (red), resulting in a red colony color. The AR mutant's more intense coloration indicates higher c-di-GMP accumulation than in the WT. Representative fluorescence microscopy of individual WT and AR mutant cells. Images were captured on a Nikon Eclipse TE2000-U microscope using the following excitation/emission wavelengths: 489/519 nm for AmCyan (green) and 553/574 nm for TurboRFP (red). Gray images are intensity surface plots corresponding to the fluorescence emitted by TurboRFP. Images were processed using Nikon NIS Elements software. All images shown are representative of three independent experiments. Scale bars, 10 mm (colonies); 10 μm (individual cells). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Figure Legend Snippet: A. brasilense AR mutant exhibits elevated levels of intracellular c-di-GMP. Colony morphology of wild-type A. brasilense Sp7 ( A ) and the AR mutant ( B ) expressing a c-di-GMP biosensor (pFY4535). Cultures were grown for five days at 30 °C on Nfb∗ agar supplemented with KNO 3 . The intracellular c-di-GMP concentration is proportional to the expression of TurboRFP (red), resulting in a red colony color. The AR mutant's more intense coloration indicates higher c-di-GMP accumulation than in the WT. Representative fluorescence microscopy of individual WT and AR mutant cells. Images were captured on a Nikon Eclipse TE2000-U microscope using the following excitation/emission wavelengths: 489/519 nm for AmCyan (green) and 553/574 nm for TurboRFP (red). Gray images are intensity surface plots corresponding to the fluorescence emitted by TurboRFP. Images were processed using Nikon NIS Elements software. All images shown are representative of three independent experiments. Scale bars, 10 mm (colonies); 10 μm (individual cells). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Techniques Used: Mutagenesis, Expressing, Concentration Assay, Fluorescence, Microscopy, Software

    Related Articles

    Software:

    Article Title: Inactivation of Cysteine Synthase CysK-A enhances flocculation, biofilm formation, and sensitivity to oxidative stress in Azospirillum brasilense Sp7
    Article Snippet: .. Obtained images were processed and analyzed using Nikon NIS Elements software. ..

    Article Title: Optimal male fertility and fecundity in Caenorhabditis elegans requires Microprocessor and Argonaute gene function.
    Article Snippet: Images were acquired using an 2 ORCA-Fusion BT camera (HAMAMATSU) with Z-stacking to capture the entire 3 germline. .. Image analysis was performed using Nikon NIS-Elements software. .. The analysis between control and mutants was conducted with unpaired T-test or 6 ANOVA followed by Dunnett, Dunnett’s T3, or Tukey’ test using GraphPad Prism 7 software.

    Article Title: DYN-1 regulates SPD-2 and PLK-1 localization and mitotic spindle pole organization
    Article Snippet: .. To analyze PLK-1::sfGFP persistence at centrosomes at different cell cycle stages, maximum intensity Z-projections of each timelapse sequence were quantified for centrosome-localized PLK-1::sfGFP using the Nikon NIS-Elements software (Nikon Instruments). ..

    Article Title: DYN-1 regulates SPD-2 and PLK-1 localization and mitotic spindle pole organization
    Article Snippet: .. To quantify PLK-1::sfGFP fluorescence at the centrosomes, maximum intensity Z-projections of metaphase embryos were generated and analyzed using Nikon NIS-Elements software (Nikon Instruments). ..

    Article Title: DYN-1 regulates SPD-2 and PLK-1 localization and mitotic spindle pole organization
    Article Snippet: .. PLK-1 localization at the midbody was quantified using a blinded, randomized analysis using maximum intensity Z-projections that were generated with the Nikon NIS-Elements software (Nikon Instruments). ..



    Article Title: DYN-1 regulates SPD-2 and PLK-1 localization and mitotic spindle pole organization
    Article Snippet: To measure spindle pole area, the CellSens software (Olympus America) was used to obtain maximum intensity Z-projections of the original .vsi files. .. These Z-projections were saved in a .png format with the fixed scaling (left:80 and right:400) for all images and further analyzed using the Nikon NIS-Elements software (Nikon Instruments). ..

    Sequencing:

    Article Title: DYN-1 regulates SPD-2 and PLK-1 localization and mitotic spindle pole organization
    Article Snippet: .. To analyze PLK-1::sfGFP persistence at centrosomes at different cell cycle stages, maximum intensity Z-projections of each timelapse sequence were quantified for centrosome-localized PLK-1::sfGFP using the Nikon NIS-Elements software (Nikon Instruments). ..

    Fluorescence:

    Article Title: DYN-1 regulates SPD-2 and PLK-1 localization and mitotic spindle pole organization
    Article Snippet: .. To quantify PLK-1::sfGFP fluorescence at the centrosomes, maximum intensity Z-projections of metaphase embryos were generated and analyzed using Nikon NIS-Elements software (Nikon Instruments). ..

    Generated:

    Article Title: DYN-1 regulates SPD-2 and PLK-1 localization and mitotic spindle pole organization
    Article Snippet: .. To quantify PLK-1::sfGFP fluorescence at the centrosomes, maximum intensity Z-projections of metaphase embryos were generated and analyzed using Nikon NIS-Elements software (Nikon Instruments). ..

    Article Title: DYN-1 regulates SPD-2 and PLK-1 localization and mitotic spindle pole organization
    Article Snippet: .. PLK-1 localization at the midbody was quantified using a blinded, randomized analysis using maximum intensity Z-projections that were generated with the Nikon NIS-Elements software (Nikon Instruments). ..



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    Nikon nikon nis elements software
    A. brasilense AR mutant exhibits elevated levels of intracellular c-di-GMP. Colony morphology of wild-type A. brasilense Sp7 ( A ) and the AR mutant ( B ) expressing a c-di-GMP biosensor (pFY4535). Cultures were grown for five days at 30 °C on Nfb∗ agar supplemented with KNO 3 . The intracellular c-di-GMP concentration is proportional to the expression of TurboRFP (red), resulting in a red colony color. The AR mutant's more intense coloration indicates higher c-di-GMP accumulation than in the WT. Representative fluorescence microscopy of individual WT and AR mutant cells. Images were captured on a Nikon Eclipse TE2000-U microscope using the following excitation/emission wavelengths: 489/519 nm for AmCyan (green) and 553/574 nm for TurboRFP (red). Gray images are intensity surface plots corresponding to the fluorescence emitted by TurboRFP. Images were processed using Nikon <t>NIS</t> <t>Elements</t> <t>software.</t> All images shown are representative of three independent experiments. Scale bars, 10 mm (colonies); 10 μm (individual cells). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Nikon Nis Elements Software, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nikon+nis+elements+software/NIS-Elements/pmc12811640-111-7-7
    Average 99 stars, based on 1 article reviews
    nikon nis elements software - by Bioz Stars, 2026-09
    99/100 stars
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    nikon imaging software nis element  (Nikon)
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    Nikon nikon imaging software nis element
    A. brasilense AR mutant exhibits elevated levels of intracellular c-di-GMP. Colony morphology of wild-type A. brasilense Sp7 ( A ) and the AR mutant ( B ) expressing a c-di-GMP biosensor (pFY4535). Cultures were grown for five days at 30 °C on Nfb∗ agar supplemented with KNO 3 . The intracellular c-di-GMP concentration is proportional to the expression of TurboRFP (red), resulting in a red colony color. The AR mutant's more intense coloration indicates higher c-di-GMP accumulation than in the WT. Representative fluorescence microscopy of individual WT and AR mutant cells. Images were captured on a Nikon Eclipse TE2000-U microscope using the following excitation/emission wavelengths: 489/519 nm for AmCyan (green) and 553/574 nm for TurboRFP (red). Gray images are intensity surface plots corresponding to the fluorescence emitted by TurboRFP. Images were processed using Nikon <t>NIS</t> <t>Elements</t> <t>software.</t> All images shown are representative of three independent experiments. Scale bars, 10 mm (colonies); 10 μm (individual cells). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Nikon Imaging Software Nis Element, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nikon+nis+elements+software/NIS-Elements/pmc13044566-129-2-2
    Average 99 stars, based on 1 article reviews
    nikon imaging software nis element - by Bioz Stars, 2026-09
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    Image Search Results


    A. brasilense AR mutant exhibits elevated levels of intracellular c-di-GMP. Colony morphology of wild-type A. brasilense Sp7 ( A ) and the AR mutant ( B ) expressing a c-di-GMP biosensor (pFY4535). Cultures were grown for five days at 30 °C on Nfb∗ agar supplemented with KNO 3 . The intracellular c-di-GMP concentration is proportional to the expression of TurboRFP (red), resulting in a red colony color. The AR mutant's more intense coloration indicates higher c-di-GMP accumulation than in the WT. Representative fluorescence microscopy of individual WT and AR mutant cells. Images were captured on a Nikon Eclipse TE2000-U microscope using the following excitation/emission wavelengths: 489/519 nm for AmCyan (green) and 553/574 nm for TurboRFP (red). Gray images are intensity surface plots corresponding to the fluorescence emitted by TurboRFP. Images were processed using Nikon NIS Elements software. All images shown are representative of three independent experiments. Scale bars, 10 mm (colonies); 10 μm (individual cells). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Biofilm

    Article Title: Inactivation of Cysteine Synthase CysK-A enhances flocculation, biofilm formation, and sensitivity to oxidative stress in Azospirillum brasilense Sp7

    doi: 10.1016/j.bioflm.2025.100335

    Figure Lengend Snippet: A. brasilense AR mutant exhibits elevated levels of intracellular c-di-GMP. Colony morphology of wild-type A. brasilense Sp7 ( A ) and the AR mutant ( B ) expressing a c-di-GMP biosensor (pFY4535). Cultures were grown for five days at 30 °C on Nfb∗ agar supplemented with KNO 3 . The intracellular c-di-GMP concentration is proportional to the expression of TurboRFP (red), resulting in a red colony color. The AR mutant's more intense coloration indicates higher c-di-GMP accumulation than in the WT. Representative fluorescence microscopy of individual WT and AR mutant cells. Images were captured on a Nikon Eclipse TE2000-U microscope using the following excitation/emission wavelengths: 489/519 nm for AmCyan (green) and 553/574 nm for TurboRFP (red). Gray images are intensity surface plots corresponding to the fluorescence emitted by TurboRFP. Images were processed using Nikon NIS Elements software. All images shown are representative of three independent experiments. Scale bars, 10 mm (colonies); 10 μm (individual cells). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: Obtained images were processed and analyzed using Nikon NIS Elements software.

    Techniques: Mutagenesis, Expressing, Concentration Assay, Fluorescence, Microscopy, Software