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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 39798 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nikon+nis+software/NIS-Elements/pmc12811640-111-7-7
    Average 99 stars, based on 39798 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: Comparison of 5 BMPs for their chondrogenic potentials and microfracture-mediated cartilage repair using heparin/PEAD coacervate sustained release polymer.
    Article Snippet: Histology and immunohistochemistry images were captured using a NIKON-Ti microscope. .. The positive Alcian blue, Safranin O, and COL2 and COL10 matrix were quantified using Nikon NIS software, by defining views of the interest of the pellets and then picking up blue, orange-red, or brown pixels and expressing these as percentages of total pellet area, respectively. ..

    Article Title: Enzymatic Bimetallic Cu-Ni Micromotor Sensor for Xanthine Detection
    Article Snippet: Enzymatic bimetallic Cu-Ni micromotors modified screen-printed electrodes were designed for the determination of xanthine.. The bimetallic Cu-Ni micromotors were prepared by electrochemical template deposition.. Morphological and structural characterization revealed that the smaller size and active mobility of the particles contribute to a larger specific surface area.

    Article Title: Senescence of endothelial cells increases susceptibility to Kaposi’s sarcoma–associated herpesvirus infection via CD109-mediated viral entry
    Article Snippet: Stained coverslips were mounted onto glass slides and analyzed using a ZEISS LSM 880 confocal microscope (ZEISS), with subsequent analysis by ZEISS Zen Blue Edition software. .. Particles were quantified using Nikon NIS software (Nikon). ..

    Article Title: Senescence of endothelial cells increases susceptibility to Kaposi’s sarcoma–associated herpesvirus infection via CD109-mediated viral entry
    Article Snippet: Stained cells were visualized by an E300 fluorescence microscope (Nikon). .. Images and particle counts were analyzed by Nikon NIS software (Nikon). .. Mouse anti-KSHV K8.1 antibody (1:100 dilution; SC-65446; 4A4; Santa Cruz Biotechnology), rabbit anti-caveolin-1 (1:100 dilution; A1555; Abclonal), rabbit anti-CD109 (1:100 dilution; 486955; E8L2W; Cell Signaling Technology), rat anti-LANA (1:100 dilution; Ab4103; LN53; Abcam), and mouse anti-KSHV ORF 65 (1:100 dilution) ( ) were used as primary antibodies.

    Article Title: Elevated nonhomologous end-joining by AATF enables efficient DNA damage repair and therapeutic resistance in glioblastoma.
    Article Snippet: Immunoprecipitation and mass spectrometric analysis Cells were collected and lysed in NP-40 lysis buffer (Boster biological technology, AR0107) supplemented with protease inhibitors and phosphatase inhibitors, incubated on ice for 30min, and followed by centrifugation at 15,000×g for 15min at 4 °C. .. Cells were then imaged using the Nikon TIE microscope and the Nikon NIS software at indicated time. ..

    Article Title: Non-canonical Wnt signaling promotes epithelial fluidization in the repairing airway
    Article Snippet: .. Data Policy information about availability of data All manuscripts must include a data availability statement This statement should provide the following information, where applicable: - Accession codes, unique identifiers, or web links for publicly available datasets - A description of any restrictions on data availability - For clinical datasets or third party data, please ensure that the statement adheres to our policy Jasper, Heinrich Hu, Daniel JK Apr 10, 2025 Intelligent Imaging 3i Slidebook and Nikon NIS software were used for microscopy. .. Data Policy information about availability of data All manuscripts must include a data availability statement This statement should provide the following information, where applicable: - Accession codes, unique identifiers, or web links for publicly available datasets - A description of any restrictions on data availability - For clinical datasets or third party data, please ensure that the statement adheres to our policy Jasper, Heinrich Hu, Daniel JK Apr 10, 2025 Intelligent Imaging 3i Slidebook and Nikon NIS software were used for microscopy.

    Article Title: Intergenerational control of ribosomes under dietary restriction
    Article Snippet: All time lapse imaging was conducted on a Nikon Ti2 epifluorescence microscope equipped with a Hamamatsu Flash 4 sCMOS camera using a 10x air objective (NA =0.45). .. Software-based autofocus was performed at each time point using the default parameters in Nikon NIS software. .. GFP excitation was at 470 nm, and mCherry excitation was at 575 nm, with 10 ms exposure times using a SpectraX light source (Lumencor).

    Article Title: Inactive ryanodine receptors sustain lysosomal availability for autophagy by promoting ER-lysosomal contact site formation
    Article Snippet: Reconstructing the images was performed using the Nikon NIS software. .. Reconstructing the images was performed using the Nikon NIS software. .. For MAP2 and SATB2 imaging, confocal images were captured using a 63×1.4 NA oil immersion objective on a Zeiss LSM510 confocal microscope with laser excitation at 543 nm and emission detection with a LP560 filter and with laser excitation at 488 nm and emission detection at 530 nm using a BP505-530 filter.

    Expressing:

    Article Title: Comparison of 5 BMPs for their chondrogenic potentials and microfracture-mediated cartilage repair using heparin/PEAD coacervate sustained release polymer.
    Article Snippet: Histology and immunohistochemistry images were captured using a NIKON-Ti microscope. .. The positive Alcian blue, Safranin O, and COL2 and COL10 matrix were quantified using Nikon NIS software, by defining views of the interest of the pellets and then picking up blue, orange-red, or brown pixels and expressing these as percentages of total pellet area, respectively. ..

    Microscopy:

    Article Title: Enzymatic Bimetallic Cu-Ni Micromotor Sensor for Xanthine Detection
    Article Snippet: Enzymatic bimetallic Cu-Ni micromotors modified screen-printed electrodes were designed for the determination of xanthine.. The bimetallic Cu-Ni micromotors were prepared by electrochemical template deposition.. Morphological and structural characterization revealed that the smaller size and active mobility of the particles contribute to a larger specific surface area.

    Article Title: Elevated nonhomologous end-joining by AATF enables efficient DNA damage repair and therapeutic resistance in glioblastoma.
    Article Snippet: Immunoprecipitation and mass spectrometric analysis Cells were collected and lysed in NP-40 lysis buffer (Boster biological technology, AR0107) supplemented with protease inhibitors and phosphatase inhibitors, incubated on ice for 30min, and followed by centrifugation at 15,000×g for 15min at 4 °C. .. Cells were then imaged using the Nikon TIE microscope and the Nikon NIS software at indicated time. ..

    Article Title: Non-canonical Wnt signaling promotes epithelial fluidization in the repairing airway
    Article Snippet: .. Data Policy information about availability of data All manuscripts must include a data availability statement This statement should provide the following information, where applicable: - Accession codes, unique identifiers, or web links for publicly available datasets - A description of any restrictions on data availability - For clinical datasets or third party data, please ensure that the statement adheres to our policy Jasper, Heinrich Hu, Daniel JK Apr 10, 2025 Intelligent Imaging 3i Slidebook and Nikon NIS software were used for microscopy. .. Data Policy information about availability of data All manuscripts must include a data availability statement This statement should provide the following information, where applicable: - Accession codes, unique identifiers, or web links for publicly available datasets - A description of any restrictions on data availability - For clinical datasets or third party data, please ensure that the statement adheres to our policy Jasper, Heinrich Hu, Daniel JK Apr 10, 2025 Intelligent Imaging 3i Slidebook and Nikon NIS software were used for microscopy.

    Imaging:

    Article Title: Non-canonical Wnt signaling promotes epithelial fluidization in the repairing airway
    Article Snippet: .. Data Policy information about availability of data All manuscripts must include a data availability statement This statement should provide the following information, where applicable: - Accession codes, unique identifiers, or web links for publicly available datasets - A description of any restrictions on data availability - For clinical datasets or third party data, please ensure that the statement adheres to our policy Jasper, Heinrich Hu, Daniel JK Apr 10, 2025 Intelligent Imaging 3i Slidebook and Nikon NIS software were used for microscopy. .. Data Policy information about availability of data All manuscripts must include a data availability statement This statement should provide the following information, where applicable: - Accession codes, unique identifiers, or web links for publicly available datasets - A description of any restrictions on data availability - For clinical datasets or third party data, please ensure that the statement adheres to our policy Jasper, Heinrich Hu, Daniel JK Apr 10, 2025 Intelligent Imaging 3i Slidebook and Nikon NIS software were used for microscopy.



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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+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
      Buy from Supplier

    99
    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+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
    99/100 stars
      Buy from Supplier

    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