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image-pro plus version 6.3 software  (Roper Technologies)

 
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    Roper Technologies image-pro plus version 6.3 software
    Image Pro Plus Version 6.3 Software, supplied by Roper Technologies, 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/product/image-pro+plus+software%2C+version+6%2E3/image+pro+plus+software/pm39499308-55-20-25
    Average 90 stars, based on 1 article reviews
    image-pro plus version 6.3 software - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Incubation:

    Article Title: Fingolimod ameliorates chronic experimental autoimmune neuritis by modulating inflammatory cytokines and Akt/mTOR/NF-κB signaling.
    Article Snippet: After three washes in TBST, bound antibodies were detected by incubation with the corresponding secondary antibodies (1:50,000) for 1 h. Data were analyzed using Image-Pro Plus software, version 6.3 (Media Cybernetics, Inc., Rockville, MD, USA).

    Software:

    Article Title: Fingolimod ameliorates chronic experimental autoimmune neuritis by modulating inflammatory cytokines and Akt/mTOR/NF-κB signaling.
    Article Snippet: After three washes in TBST, bound antibodies were detected by incubation with the corresponding secondary antibodies (1:50,000) for 1 h. Data were analyzed using Image-Pro Plus software, version 6.3 (Media Cybernetics, Inc., Rockville, MD, USA).



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    Image Search Results


    Effects of Cr(VI) exposure on abnormal microtubule structure and F-actin expression. Prepubertal rats were exposed to 1 ppm or 5 ppm potassium dichromate through drinking water from PND 22 to 29 and superovulated. Immunofluorescence was performed in the MII oocytes. ( A ) The number of oocytes with dispersed chromosomes and abnormal microtubules was counted and expressed as a percentage. Each value is mean ± SEM of 100 oocytes from 10 rats. ( B ) Expression of F-actin was determined by immunofluorescence. Images were captured by confocal microscopy and quantified using Image-Pro Plus software, Version 10.0.5 (Media Cybernetics Inc.). a: control vs. Cr(VI) 1 ppm or 5 ppm; b: Cr(VI) 1 ppm vs. 5 ppm; p < 0.05.

    Journal: International Journal of Molecular Sciences

    Article Title: Hexavalent Chromium Disrupts Oocyte Development in Rats by Elevating Oxidative Stress, DNA Double-Strand Breaks, Microtubule Disruption, and Aberrant Segregation of Chromosomes

    doi: 10.3390/ijms241210003

    Figure Lengend Snippet: Effects of Cr(VI) exposure on abnormal microtubule structure and F-actin expression. Prepubertal rats were exposed to 1 ppm or 5 ppm potassium dichromate through drinking water from PND 22 to 29 and superovulated. Immunofluorescence was performed in the MII oocytes. ( A ) The number of oocytes with dispersed chromosomes and abnormal microtubules was counted and expressed as a percentage. Each value is mean ± SEM of 100 oocytes from 10 rats. ( B ) Expression of F-actin was determined by immunofluorescence. Images were captured by confocal microscopy and quantified using Image-Pro Plus software, Version 10.0.5 (Media Cybernetics Inc.). a: control vs. Cr(VI) 1 ppm or 5 ppm; b: Cr(VI) 1 ppm vs. 5 ppm; p < 0.05.

    Article Snippet: The intensity of staining for 8-OHdG, NTY, γ-H2AX, and RAD51 was quantified using Image-Pro Plus 6.3 software, Version 10.0.5 (Media Cybernetics, Inc., Bethesda, MD, USA) and expressed as Integrated Optical Density (IOD) according to the manufacturer’s instructions.

    Techniques: Expressing, Immunofluorescence, Confocal Microscopy, Software

    Effects of Cr(VI) exposure on oxidative protein damage in MII oocytes. Prepubertal rats were exposed to 1 or 5 ppm potassium dichromate through drinking water from PND 22 to 29 and superovulated. Nitrotyrosine, a biomarker of oxidative protein damage, was determined by immunofluorescence in the MII oocytes. Images were captured by confocal microscopy; all images were captured with a 40×/1.4 NA Plan-Apochromat lens and the width of each field is 70 µm. Images quantified using Image-Pro Plus software, Version 10.0.5 (Media Cybernetics Inc.). Cr(VI) increased NTY expression. Representative images of the control ( A – D ), 1 ppm Cr(VI) ( E – H ), and 5 ppm Cr(VI) ( I – L ) groups are shown. The histogram ( M ) represents the intensity of staining (expressed as Integrated Optical Density (IOD)). Each value is mean ± SEM of ~24 oocytes from six rats ( p < 0.05). a: control vs. Cr(VI) 1 ppm or 5 ppm.

    Journal: International Journal of Molecular Sciences

    Article Title: Hexavalent Chromium Disrupts Oocyte Development in Rats by Elevating Oxidative Stress, DNA Double-Strand Breaks, Microtubule Disruption, and Aberrant Segregation of Chromosomes

    doi: 10.3390/ijms241210003

    Figure Lengend Snippet: Effects of Cr(VI) exposure on oxidative protein damage in MII oocytes. Prepubertal rats were exposed to 1 or 5 ppm potassium dichromate through drinking water from PND 22 to 29 and superovulated. Nitrotyrosine, a biomarker of oxidative protein damage, was determined by immunofluorescence in the MII oocytes. Images were captured by confocal microscopy; all images were captured with a 40×/1.4 NA Plan-Apochromat lens and the width of each field is 70 µm. Images quantified using Image-Pro Plus software, Version 10.0.5 (Media Cybernetics Inc.). Cr(VI) increased NTY expression. Representative images of the control ( A – D ), 1 ppm Cr(VI) ( E – H ), and 5 ppm Cr(VI) ( I – L ) groups are shown. The histogram ( M ) represents the intensity of staining (expressed as Integrated Optical Density (IOD)). Each value is mean ± SEM of ~24 oocytes from six rats ( p < 0.05). a: control vs. Cr(VI) 1 ppm or 5 ppm.

    Article Snippet: The intensity of staining for 8-OHdG, NTY, γ-H2AX, and RAD51 was quantified using Image-Pro Plus 6.3 software, Version 10.0.5 (Media Cybernetics, Inc., Bethesda, MD, USA) and expressed as Integrated Optical Density (IOD) according to the manufacturer’s instructions.

    Techniques: Biomarker Assay, Immunofluorescence, Confocal Microscopy, Software, Expressing, Staining

    Effects of Cr(VI) exposure on DNA double-strand breaks. Prepubertal rats were exposed to 1 or 5 ppm potassium dichromate through drinking water from PND 22 to 29 and superovulated. γ-H2AX, the DNA DSB marker, was determined by immunofluorescence. All confocal images were captured with a 40×/1.4 NA Plan-Apochromat lens and the width of each field is 25 µm. Images were quantified using Image-Pro Plus software, Version 10.0.5 (Media Cybernetics Inc.). Representative images of the control ( A – E ), 1 ppm Cr(VI) ( F – J ), and 5 ppm Cr(VI) ( K – O ) groups are shown. The histogram ( P ) represents the intensity of staining (expressed as Integrated Optical Density (IOD)). Each value is mean ± SEM of ~24 oocytes from six rats ( p < 0.05). a: control vs. Cr(VI) 1 ppm or 5 ppm; b: Cr(VI) 1 ppm vs. 5 ppm.

    Journal: International Journal of Molecular Sciences

    Article Title: Hexavalent Chromium Disrupts Oocyte Development in Rats by Elevating Oxidative Stress, DNA Double-Strand Breaks, Microtubule Disruption, and Aberrant Segregation of Chromosomes

    doi: 10.3390/ijms241210003

    Figure Lengend Snippet: Effects of Cr(VI) exposure on DNA double-strand breaks. Prepubertal rats were exposed to 1 or 5 ppm potassium dichromate through drinking water from PND 22 to 29 and superovulated. γ-H2AX, the DNA DSB marker, was determined by immunofluorescence. All confocal images were captured with a 40×/1.4 NA Plan-Apochromat lens and the width of each field is 25 µm. Images were quantified using Image-Pro Plus software, Version 10.0.5 (Media Cybernetics Inc.). Representative images of the control ( A – E ), 1 ppm Cr(VI) ( F – J ), and 5 ppm Cr(VI) ( K – O ) groups are shown. The histogram ( P ) represents the intensity of staining (expressed as Integrated Optical Density (IOD)). Each value is mean ± SEM of ~24 oocytes from six rats ( p < 0.05). a: control vs. Cr(VI) 1 ppm or 5 ppm; b: Cr(VI) 1 ppm vs. 5 ppm.

    Article Snippet: The intensity of staining for 8-OHdG, NTY, γ-H2AX, and RAD51 was quantified using Image-Pro Plus 6.3 software, Version 10.0.5 (Media Cybernetics, Inc., Bethesda, MD, USA) and expressed as Integrated Optical Density (IOD) according to the manufacturer’s instructions.

    Techniques: Marker, Immunofluorescence, Software, Staining

    Effects of Cr(VI) exposure on DNA damage repair protein RAD51. Prepubertal rats were exposed to 1 or 5 ppm potassium dichromate through drinking water from PND 22 to 29 and superovulated. RAD51, a DNA damage repair protein, was determined by immunofluorescence. All confocal images were captured with a 40×/1.4 NA Plan-Apochromat lens and the width of each field is 35 µm. Images were quantified using Image-Pro Plus software, Version 10.0.5 (Media Cybernetics Inc.). Representative images of the control ( A – E ), 1 ppm Cr(VI) ( F – J ), and 5 ppm Cr(VI) ( K – O ) groups are shown. The histogram ( P ) represents the intensity of staining (expressed as Integrated Optical Density (IOD)). Each value is mean ± SEM of ~24 oocytes from six rats ( p < 0.05). a: control vs. Cr(VI) 1 ppm or 5 ppm; b: Cr(VI) 1 ppm vs. 5 ppm.

    Journal: International Journal of Molecular Sciences

    Article Title: Hexavalent Chromium Disrupts Oocyte Development in Rats by Elevating Oxidative Stress, DNA Double-Strand Breaks, Microtubule Disruption, and Aberrant Segregation of Chromosomes

    doi: 10.3390/ijms241210003

    Figure Lengend Snippet: Effects of Cr(VI) exposure on DNA damage repair protein RAD51. Prepubertal rats were exposed to 1 or 5 ppm potassium dichromate through drinking water from PND 22 to 29 and superovulated. RAD51, a DNA damage repair protein, was determined by immunofluorescence. All confocal images were captured with a 40×/1.4 NA Plan-Apochromat lens and the width of each field is 35 µm. Images were quantified using Image-Pro Plus software, Version 10.0.5 (Media Cybernetics Inc.). Representative images of the control ( A – E ), 1 ppm Cr(VI) ( F – J ), and 5 ppm Cr(VI) ( K – O ) groups are shown. The histogram ( P ) represents the intensity of staining (expressed as Integrated Optical Density (IOD)). Each value is mean ± SEM of ~24 oocytes from six rats ( p < 0.05). a: control vs. Cr(VI) 1 ppm or 5 ppm; b: Cr(VI) 1 ppm vs. 5 ppm.

    Article Snippet: The intensity of staining for 8-OHdG, NTY, γ-H2AX, and RAD51 was quantified using Image-Pro Plus 6.3 software, Version 10.0.5 (Media Cybernetics, Inc., Bethesda, MD, USA) and expressed as Integrated Optical Density (IOD) according to the manufacturer’s instructions.

    Techniques: Immunofluorescence, Software, Staining