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cellsens dimension 1 7 imaging software  (Olympus)


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    Structured Review

    Olympus cellsens dimension 1 7 imaging software
    Cellsens Dimension 1 7 Imaging Software, supplied by Olympus, used in various techniques. Bioz Stars score: 99/100, based on 20104 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cellsens+imaging+software+program/BX53+System+Microscope/pm32002604-108-24-31
    Average 99 stars, based on 20104 article reviews
    cellsens dimension 1 7 imaging software - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    Microscopy:

    Article Title: Adsorptive Removal of 1,2-Dichloroethane Using Novel Oleogel Adsorbents: Synthesis Strategy and Adsorption Mechanism Insight.
    Article Snippet: Macroscopic morphology was studied using a Canon PowerShot G1 X Mark III digital camera used to assess sample appearance and self-supporting ability. .. OM observations were carried out using an Olympus BX53 optical microscope (Olympus, Japan) equipped with bright-field illumination at 100× magnification to examine the surface topography and microstructure of Oleogel samples. .. PLM (Olympus GX71, Japan) was used to visualize the crystalline network structure of the oleogels.

    Article Title: Arabidopsis cyclin-dependent kinases and MAP65 phosphorylation link microtubule dynamics with salt stress adaptation.
    Article Snippet: Xiaoxiao Qu* , Junjie Zou* , Chunxia Zhang , Junling Yue , Kezhen Yang and Jie Le State Key Laboratory of Forage Breeding-by-Design and Utilization, Key Laboratory of Plant Molecular Physiology, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China; University of Chinese Academy of Sciences, Beijing, 100049, China; State Key Laboratory of Seed Innovation, Institute of Genetics and Developmental Biology, Chinese Academy of

    Article Title: Wnt10b is required for the increase in cancellous bone caused by oxidized phospholipids blockade.
    Article Snippet: Sections were counterstained with hematoxylin, dehydrated at 60°C for 20 min, and mounted using VectaMount Permanent Mounting Medium (Vector Laboratories, Newark, CA, USA). .. Histomorphometric quantification of Wnt10b in situ hybridization signal was expressed as Wnt10b-positive surface per bone Jo ur na l P re -p ro of surface (Wnt10b S/BS) and performed using an Olympus BX53 microscope in conjunction with OsteoMeasure software (OsteoMetrics, Inc., Decatur, GA, USA). ..

    Article Title: Cell wall metabolism and cellular structure synergistically regulate texture in jujube fruit: implications for quality classification and processing adaptability.
    Article Snippet: The following day, after embedding and polymerization, the samples were sectioned, stained with uranyl acetate and lead citrate, and observed using a Hitachi TEM system. .. Images of jujube pulp cell sections were acquired using a BX53 fluorescence microscopy (Olympus Corporation, Tokyo, Japan) and analyzed and measured using the OLYMPUS-cellsens 2.1 system (Build 17342). ..

    Article Title: Cell-type-specific PIN-FORMED 3-mediated polar auxin transport regulates cambial activity and tension wood formation in Populus tomentosa.
    Article Snippet: Auxin is a central regulator of tree secondary growth and forms maxima in the vascular cambium, yet how these maxima are established remains elusive.. Here, we functionally characterized two redundant PIN-FORMED 3 (PIN3) paralogs from Populus tomentosa to define their roles in secondary growth and gravity-induced tension wood (TW) formation.. We employed fluorescent reporter lines, clustered regularly interspaced short palindromic repeats-generated knockout mutants, phloem-specific RNA interference transgenic plants and isotopic auxin transport assays to dissect PIN3 functions during secondary growth of poplar stems.

    Article Title: Polyomavirus Drives Cerebellar Lesions in AIDS Monkeys With Ataxia
    Article Snippet: .. Histopathological changes were assessed using hematoxylin and eosin (H&E), Luxol fast blue (LFB), PAS, and Gram staining, followed by imaging with a brightfield microscope (BX53, Olympus, Japan). ..

    Article Title: Effect of Microcurrent Stimulation on Cartilage Regeneration in Engineered Chondrocyte Spheroids.
    Article Snippet: Immunoreactivity was visualized using 3,3′- diaminobenzidine (DAB) substrate (Vector Laboratories, Burlingame, CA, USA), and nuclei were counterstained with hematoxylin. .. All stained sections were imaged using a bright-field microscope (BX53, Olympus, Tokyo, Japan) equipped with a digital camera. .. For quantitative analysis, the positive staining area or staining intensity of COL 2026 II and the histological appearance of TB and Safranin O staining were analyzed using ImageJ software under identical imaging settings

    Surface Topography:

    Article Title: Adsorptive Removal of 1,2-Dichloroethane Using Novel Oleogel Adsorbents: Synthesis Strategy and Adsorption Mechanism Insight.
    Article Snippet: Macroscopic morphology was studied using a Canon PowerShot G1 X Mark III digital camera used to assess sample appearance and self-supporting ability. .. OM observations were carried out using an Olympus BX53 optical microscope (Olympus, Japan) equipped with bright-field illumination at 100× magnification to examine the surface topography and microstructure of Oleogel samples. .. PLM (Olympus GX71, Japan) was used to visualize the crystalline network structure of the oleogels.

    Incubation:

    Article Title: Arabidopsis cyclin-dependent kinases and MAP65 phosphorylation link microtubule dynamics with salt stress adaptation.
    Article Snippet: Xiaoxiao Qu* , Junjie Zou* , Chunxia Zhang , Junling Yue , Kezhen Yang and Jie Le State Key Laboratory of Forage Breeding-by-Design and Utilization, Key Laboratory of Plant Molecular Physiology, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China; University of Chinese Academy of Sciences, Beijing, 100049, China; State Key Laboratory of Seed Innovation, Institute of Genetics and Developmental Biology, Chinese Academy of

    In Situ Hybridization:

    Article Title: Wnt10b is required for the increase in cancellous bone caused by oxidized phospholipids blockade.
    Article Snippet: Sections were counterstained with hematoxylin, dehydrated at 60°C for 20 min, and mounted using VectaMount Permanent Mounting Medium (Vector Laboratories, Newark, CA, USA). .. Histomorphometric quantification of Wnt10b in situ hybridization signal was expressed as Wnt10b-positive surface per bone Jo ur na l P re -p ro of surface (Wnt10b S/BS) and performed using an Olympus BX53 microscope in conjunction with OsteoMeasure software (OsteoMetrics, Inc., Decatur, GA, USA). ..

    Software:

    Article Title: Wnt10b is required for the increase in cancellous bone caused by oxidized phospholipids blockade.
    Article Snippet: Sections were counterstained with hematoxylin, dehydrated at 60°C for 20 min, and mounted using VectaMount Permanent Mounting Medium (Vector Laboratories, Newark, CA, USA). .. Histomorphometric quantification of Wnt10b in situ hybridization signal was expressed as Wnt10b-positive surface per bone Jo ur na l P re -p ro of surface (Wnt10b S/BS) and performed using an Olympus BX53 microscope in conjunction with OsteoMeasure software (OsteoMetrics, Inc., Decatur, GA, USA). ..

    other:

    Article Title: KRIT1 Inhibits TGF-β/Smad-Mediated Endothelial-To-Mesenchymal Transition in Pulmonary Arterial Hypertension.
    Article Snippet: Staining was conducted with eosin solution (A600190, Sangon, China) for 3 min. After dehydration in a graded ethanol series and clearing in xylene, the sections were mounted with neutral balsam and imaged under a microscope (BX53, Olympus, Japan).

    Fluorescence:

    Article Title: Cell wall metabolism and cellular structure synergistically regulate texture in jujube fruit: implications for quality classification and processing adaptability.
    Article Snippet: The following day, after embedding and polymerization, the samples were sectioned, stained with uranyl acetate and lead citrate, and observed using a Hitachi TEM system. .. Images of jujube pulp cell sections were acquired using a BX53 fluorescence microscopy (Olympus Corporation, Tokyo, Japan) and analyzed and measured using the OLYMPUS-cellsens 2.1 system (Build 17342). ..

    Analysis:

    Article Title: Cell-type-specific PIN-FORMED 3-mediated polar auxin transport regulates cambial activity and tension wood formation in Populus tomentosa.
    Article Snippet: Auxin is a central regulator of tree secondary growth and forms maxima in the vascular cambium, yet how these maxima are established remains elusive.. Here, we functionally characterized two redundant PIN-FORMED 3 (PIN3) paralogs from Populus tomentosa to define their roles in secondary growth and gravity-induced tension wood (TW) formation.. We employed fluorescent reporter lines, clustered regularly interspaced short palindromic repeats-generated knockout mutants, phloem-specific RNA interference transgenic plants and isotopic auxin transport assays to dissect PIN3 functions during secondary growth of poplar stems.

    Staining:

    Article Title: Cell-type-specific PIN-FORMED 3-mediated polar auxin transport regulates cambial activity and tension wood formation in Populus tomentosa.
    Article Snippet: Auxin is a central regulator of tree secondary growth and forms maxima in the vascular cambium, yet how these maxima are established remains elusive.. Here, we functionally characterized two redundant PIN-FORMED 3 (PIN3) paralogs from Populus tomentosa to define their roles in secondary growth and gravity-induced tension wood (TW) formation.. We employed fluorescent reporter lines, clustered regularly interspaced short palindromic repeats-generated knockout mutants, phloem-specific RNA interference transgenic plants and isotopic auxin transport assays to dissect PIN3 functions during secondary growth of poplar stems.

    Article Title: Polyomavirus Drives Cerebellar Lesions in AIDS Monkeys With Ataxia
    Article Snippet: .. Histopathological changes were assessed using hematoxylin and eosin (H&E), Luxol fast blue (LFB), PAS, and Gram staining, followed by imaging with a brightfield microscope (BX53, Olympus, Japan). ..

    Article Title: Effect of Microcurrent Stimulation on Cartilage Regeneration in Engineered Chondrocyte Spheroids.
    Article Snippet: Immunoreactivity was visualized using 3,3′- diaminobenzidine (DAB) substrate (Vector Laboratories, Burlingame, CA, USA), and nuclei were counterstained with hematoxylin. .. All stained sections were imaged using a bright-field microscope (BX53, Olympus, Tokyo, Japan) equipped with a digital camera. .. For quantitative analysis, the positive staining area or staining intensity of COL 2026 II and the histological appearance of TB and Safranin O staining were analyzed using ImageJ software under identical imaging settings

    Imaging:

    Article Title: Polyomavirus Drives Cerebellar Lesions in AIDS Monkeys With Ataxia
    Article Snippet: .. Histopathological changes were assessed using hematoxylin and eosin (H&E), Luxol fast blue (LFB), PAS, and Gram staining, followed by imaging with a brightfield microscope (BX53, Olympus, Japan). ..

    Brightfield:

    Article Title: Polyomavirus Drives Cerebellar Lesions in AIDS Monkeys With Ataxia
    Article Snippet: .. Histopathological changes were assessed using hematoxylin and eosin (H&E), Luxol fast blue (LFB), PAS, and Gram staining, followed by imaging with a brightfield microscope (BX53, Olympus, Japan). ..



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    TaWAKL8-2B positively regulates wheat resistance to Pst. A Disease phenotype of TaWAKL8 - 2B -KO plants inoculated with Pst CYR23. Representative images of disease phenotype were taken at 14 dpi. B Relative fungal biomass in TaWAKL8-2B -KO plants. The relative biomass ratio ( Pst /wheat) was assayed with DNA isolated from the leaves at 14 dpi. TaEF-1α and PstEF were used to normalize the DNA level of wheat and Pst , respectively. C Relative transcription levels of TaPR1 , TaPR2 and TaPR5 in TaWAKL8 - 2B -KO plants inoculated with CYR23. D H 2 O 2 accumulation at the infection sites in TaWAKL8 - 2B -KO plants stained with DAB at 24 and 48 hpi. E Quantification of tissue areas containing H 2 O 2 from D . F Histological observation of Pst growth and development in TaWAKL8 - 2B -KO and Fielder plants. Pst infection structures were stained with wheat germ agglutinin conjugated to Alexa-488 and observed with an Olympus BX-53 microscope. SV, substomatal vesicle; IH, infection hypha; HMC, haustorial mother cell; H, haustorium; (g) Hyphal length was measured by <t>Cellsens</t> software. Values in ( E and G ) represent the mean ± SEM from three independent samples with 90 infection sites. Error bars in ( B and C ) indicate SD from three technical replicates. Experiments were independently repeated three times with similar results. Asterisks indicate significant differences (Student’s t test, * p < 0.05, ** p < 0.01, **** p < 0.0001)
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    Image Search Results


    TaWAKL8-2B positively regulates wheat resistance to Pst. A Disease phenotype of TaWAKL8 - 2B -KO plants inoculated with Pst CYR23. Representative images of disease phenotype were taken at 14 dpi. B Relative fungal biomass in TaWAKL8-2B -KO plants. The relative biomass ratio ( Pst /wheat) was assayed with DNA isolated from the leaves at 14 dpi. TaEF-1α and PstEF were used to normalize the DNA level of wheat and Pst , respectively. C Relative transcription levels of TaPR1 , TaPR2 and TaPR5 in TaWAKL8 - 2B -KO plants inoculated with CYR23. D H 2 O 2 accumulation at the infection sites in TaWAKL8 - 2B -KO plants stained with DAB at 24 and 48 hpi. E Quantification of tissue areas containing H 2 O 2 from D . F Histological observation of Pst growth and development in TaWAKL8 - 2B -KO and Fielder plants. Pst infection structures were stained with wheat germ agglutinin conjugated to Alexa-488 and observed with an Olympus BX-53 microscope. SV, substomatal vesicle; IH, infection hypha; HMC, haustorial mother cell; H, haustorium; (g) Hyphal length was measured by Cellsens software. Values in ( E and G ) represent the mean ± SEM from three independent samples with 90 infection sites. Error bars in ( B and C ) indicate SD from three technical replicates. Experiments were independently repeated three times with similar results. Asterisks indicate significant differences (Student’s t test, * p < 0.05, ** p < 0.01, **** p < 0.0001)

    Journal: Stress Biology

    Article Title: TaWAKL8-2B, a wall-associated receptor-like kinase, mediates wheat rust resistance by linalool and ROS accumulation

    doi: 10.1007/s44154-025-00248-3

    Figure Lengend Snippet: TaWAKL8-2B positively regulates wheat resistance to Pst. A Disease phenotype of TaWAKL8 - 2B -KO plants inoculated with Pst CYR23. Representative images of disease phenotype were taken at 14 dpi. B Relative fungal biomass in TaWAKL8-2B -KO plants. The relative biomass ratio ( Pst /wheat) was assayed with DNA isolated from the leaves at 14 dpi. TaEF-1α and PstEF were used to normalize the DNA level of wheat and Pst , respectively. C Relative transcription levels of TaPR1 , TaPR2 and TaPR5 in TaWAKL8 - 2B -KO plants inoculated with CYR23. D H 2 O 2 accumulation at the infection sites in TaWAKL8 - 2B -KO plants stained with DAB at 24 and 48 hpi. E Quantification of tissue areas containing H 2 O 2 from D . F Histological observation of Pst growth and development in TaWAKL8 - 2B -KO and Fielder plants. Pst infection structures were stained with wheat germ agglutinin conjugated to Alexa-488 and observed with an Olympus BX-53 microscope. SV, substomatal vesicle; IH, infection hypha; HMC, haustorial mother cell; H, haustorium; (g) Hyphal length was measured by Cellsens software. Values in ( E and G ) represent the mean ± SEM from three independent samples with 90 infection sites. Error bars in ( B and C ) indicate SD from three technical replicates. Experiments were independently repeated three times with similar results. Asterisks indicate significant differences (Student’s t test, * p < 0.05, ** p < 0.01, **** p < 0.0001)

    Article Snippet: Quantification of H 2 O 2 -containing areas and Pst growth were performed with the cellSens Entry software program (Olympus, Tokyo, Japan).

    Techniques: Isolation, Infection, Staining, Microscopy, Software