Review



celltracker software  (Carl Zeiss)


Bioz Verified Symbol Carl Zeiss is a verified supplier
Bioz Manufacturer Symbol Carl Zeiss manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 90
      Buy from Supplier

    Structured Review

    Carl Zeiss celltracker software
    Time-lapse Confocal imaging of NF-κB nuclear translocation in Lipid A-stimulated human PBMDMs. (A) PBMC-derived macrophages from human subjects were transduced with a fluorescent lentiviral p65AmCyan construct and were used to image NF-κB p65 subunit cellular dynamics in real-time. (B) <t>CellTracker</t> was used to generate profiles of nuclear translocation of transduced cells post stimulation with 200ng/mL Lipid A, over 3h: Asterisks (*) indicate nuclear localization of p65 at 66 and 93 min (‘). (C-E) Graphs of individual nuclear translocation profiles of responding cells in the healthy controls, Crohn’s disease (CD) and ulcerative colitis (UC) groups; mean ± SD for all responsive cells shown in blue, red and green colour lines for each group, respectively. (F) The proportion of responding cells was calculated by pooling all tracked cells from each disease group; *p<0.05; two-sided Fisher’s exact test (by summation). Peak identification and analysis revealed in each population the peak time (G), peak amplitude (H) and peak width (I): *p<0.05, ***p<0.001; statistical differences assessed by Kruskal Wallis test with pairwise comparison of all three groups.
    Celltracker Software, supplied by Carl Zeiss, 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/celltracker software/product/Carl Zeiss
    Average 90 stars, based on 1 article reviews
    celltracker software - by Bioz Stars, 2026-05
    90/100 stars

    Images

    1) Product Images from "Macrophage-specific NF-κB activation dynamics can segregate inflammatory bowel disease patients"

    Article Title: Macrophage-specific NF-κB activation dynamics can segregate inflammatory bowel disease patients

    Journal: bioRxiv

    doi: 10.1101/535096

    Time-lapse Confocal imaging of NF-κB nuclear translocation in Lipid A-stimulated human PBMDMs. (A) PBMC-derived macrophages from human subjects were transduced with a fluorescent lentiviral p65AmCyan construct and were used to image NF-κB p65 subunit cellular dynamics in real-time. (B) CellTracker was used to generate profiles of nuclear translocation of transduced cells post stimulation with 200ng/mL Lipid A, over 3h: Asterisks (*) indicate nuclear localization of p65 at 66 and 93 min (‘). (C-E) Graphs of individual nuclear translocation profiles of responding cells in the healthy controls, Crohn’s disease (CD) and ulcerative colitis (UC) groups; mean ± SD for all responsive cells shown in blue, red and green colour lines for each group, respectively. (F) The proportion of responding cells was calculated by pooling all tracked cells from each disease group; *p<0.05; two-sided Fisher’s exact test (by summation). Peak identification and analysis revealed in each population the peak time (G), peak amplitude (H) and peak width (I): *p<0.05, ***p<0.001; statistical differences assessed by Kruskal Wallis test with pairwise comparison of all three groups.
    Figure Legend Snippet: Time-lapse Confocal imaging of NF-κB nuclear translocation in Lipid A-stimulated human PBMDMs. (A) PBMC-derived macrophages from human subjects were transduced with a fluorescent lentiviral p65AmCyan construct and were used to image NF-κB p65 subunit cellular dynamics in real-time. (B) CellTracker was used to generate profiles of nuclear translocation of transduced cells post stimulation with 200ng/mL Lipid A, over 3h: Asterisks (*) indicate nuclear localization of p65 at 66 and 93 min (‘). (C-E) Graphs of individual nuclear translocation profiles of responding cells in the healthy controls, Crohn’s disease (CD) and ulcerative colitis (UC) groups; mean ± SD for all responsive cells shown in blue, red and green colour lines for each group, respectively. (F) The proportion of responding cells was calculated by pooling all tracked cells from each disease group; *p<0.05; two-sided Fisher’s exact test (by summation). Peak identification and analysis revealed in each population the peak time (G), peak amplitude (H) and peak width (I): *p<0.05, ***p<0.001; statistical differences assessed by Kruskal Wallis test with pairwise comparison of all three groups.

    Techniques Used: Imaging, Translocation Assay, Derivative Assay, Transduction, Construct, Comparison



    Similar Products

    image processing software celltracker  (MathWorks Inc)
    90
    MathWorks Inc image processing software celltracker
    Image Processing Software Celltracker, supplied by MathWorks 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/image processing software celltracker/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    image processing software celltracker - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier
    celltracker software matlab r2020a  (MathWorks Inc)
    90
    MathWorks Inc celltracker software matlab r2020a
    ( A ) The top view and side view of REF 2c labeled with <t>CellTracker-Green</t> dye at 24 hr and 48 hr. Scale bar, 100 μm. ( B ) Zoomed side view of REF 2c labeled with CellTracker-Green dye at 24 hr and 48 hr. Scale bar, 10 μm. ( C ) Bar plot showing the tissue thickness at 24 hr ( n = 12) and 48 hr ( n = 12). **, p < 0.01. ( D ) Plot showing the mean thickness across the REF colony at 24 hr ( n = 12) and 48 hr ( n = 12).
    Celltracker Software Matlab R2020a, supplied by MathWorks 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/celltracker software matlab r2020a/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    celltracker software matlab r2020a - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier
    celltracker software implemented in matlab r2020a  (MathWorks Inc)
    90
    MathWorks Inc celltracker software implemented in matlab r2020a
    ( A ) The top view and side view of REF 2c labeled with <t>CellTracker-Green</t> dye at 24 hr and 48 hr. Scale bar, 100 μm. ( B ) Zoomed side view of REF 2c labeled with CellTracker-Green dye at 24 hr and 48 hr. Scale bar, 10 μm. ( C ) Bar plot showing the tissue thickness at 24 hr ( n = 12) and 48 hr ( n = 12). **, p < 0.01. ( D ) Plot showing the mean thickness across the REF colony at 24 hr ( n = 12) and 48 hr ( n = 12).
    Celltracker Software Implemented In Matlab R2020a, supplied by MathWorks 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/celltracker software implemented in matlab r2020a/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    celltracker software implemented in matlab r2020a - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier
    celltracks system imaging software  (CellSearch inc)
    90
    CellSearch inc celltracks system imaging software
    ( A ) The top view and side view of REF 2c labeled with <t>CellTracker-Green</t> dye at 24 hr and 48 hr. Scale bar, 100 μm. ( B ) Zoomed side view of REF 2c labeled with CellTracker-Green dye at 24 hr and 48 hr. Scale bar, 10 μm. ( C ) Bar plot showing the tissue thickness at 24 hr ( n = 12) and 48 hr ( n = 12). **, p < 0.01. ( D ) Plot showing the mean thickness across the REF colony at 24 hr ( n = 12) and 48 hr ( n = 12).
    Celltracks System Imaging Software, supplied by CellSearch 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/celltracks system imaging software/product/CellSearch inc
    Average 90 stars, based on 1 article reviews
    celltracks system imaging software - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier
    celltracker software  (Carl Zeiss)
    90
    Carl Zeiss celltracker software
    Time-lapse Confocal imaging of NF-κB nuclear translocation in Lipid A-stimulated human PBMDMs. (A) PBMC-derived macrophages from human subjects were transduced with a fluorescent lentiviral p65AmCyan construct and were used to image NF-κB p65 subunit cellular dynamics in real-time. (B) <t>CellTracker</t> was used to generate profiles of nuclear translocation of transduced cells post stimulation with 200ng/mL Lipid A, over 3h: Asterisks (*) indicate nuclear localization of p65 at 66 and 93 min (‘). (C-E) Graphs of individual nuclear translocation profiles of responding cells in the healthy controls, Crohn’s disease (CD) and ulcerative colitis (UC) groups; mean ± SD for all responsive cells shown in blue, red and green colour lines for each group, respectively. (F) The proportion of responding cells was calculated by pooling all tracked cells from each disease group; *p<0.05; two-sided Fisher’s exact test (by summation). Peak identification and analysis revealed in each population the peak time (G), peak amplitude (H) and peak width (I): *p<0.05, ***p<0.001; statistical differences assessed by Kruskal Wallis test with pairwise comparison of all three groups.
    Celltracker Software, supplied by Carl Zeiss, 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/celltracker software/product/Carl Zeiss
    Average 90 stars, based on 1 article reviews
    celltracker software - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier
    celltracker software  (Scherf GmbH)
    90
    Scherf GmbH celltracker software
    Time-lapse Confocal imaging of NF-κB nuclear translocation in Lipid A-stimulated human PBMDMs. (A) PBMC-derived macrophages from human subjects were transduced with a fluorescent lentiviral p65AmCyan construct and were used to image NF-κB p65 subunit cellular dynamics in real-time. (B) <t>CellTracker</t> was used to generate profiles of nuclear translocation of transduced cells post stimulation with 200ng/mL Lipid A, over 3h: Asterisks (*) indicate nuclear localization of p65 at 66 and 93 min (‘). (C-E) Graphs of individual nuclear translocation profiles of responding cells in the healthy controls, Crohn’s disease (CD) and ulcerative colitis (UC) groups; mean ± SD for all responsive cells shown in blue, red and green colour lines for each group, respectively. (F) The proportion of responding cells was calculated by pooling all tracked cells from each disease group; *p<0.05; two-sided Fisher’s exact test (by summation). Peak identification and analysis revealed in each population the peak time (G), peak amplitude (H) and peak width (I): *p<0.05, ***p<0.001; statistical differences assessed by Kruskal Wallis test with pairwise comparison of all three groups.
    Celltracker Software, supplied by Scherf GmbH, 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/celltracker software/product/Scherf GmbH
    Average 90 stars, based on 1 article reviews
    celltracker software - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier
    celltracker software  (Kinetic Imaging Ltd)
    90
    Kinetic Imaging Ltd celltracker software
    Time-lapse Confocal imaging of NF-κB nuclear translocation in Lipid A-stimulated human PBMDMs. (A) PBMC-derived macrophages from human subjects were transduced with a fluorescent lentiviral p65AmCyan construct and were used to image NF-κB p65 subunit cellular dynamics in real-time. (B) <t>CellTracker</t> was used to generate profiles of nuclear translocation of transduced cells post stimulation with 200ng/mL Lipid A, over 3h: Asterisks (*) indicate nuclear localization of p65 at 66 and 93 min (‘). (C-E) Graphs of individual nuclear translocation profiles of responding cells in the healthy controls, Crohn’s disease (CD) and ulcerative colitis (UC) groups; mean ± SD for all responsive cells shown in blue, red and green colour lines for each group, respectively. (F) The proportion of responding cells was calculated by pooling all tracked cells from each disease group; *p<0.05; two-sided Fisher’s exact test (by summation). Peak identification and analysis revealed in each population the peak time (G), peak amplitude (H) and peak width (I): *p<0.05, ***p<0.001; statistical differences assessed by Kruskal Wallis test with pairwise comparison of all three groups.
    Celltracker Software, supplied by Kinetic Imaging Ltd, 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/celltracker software/product/Kinetic Imaging Ltd
    Average 90 stars, based on 1 article reviews
    celltracker software - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier
    based software celltracker  (MathWorks Inc)
    90
    MathWorks Inc based software celltracker
    Time-lapse Confocal imaging of NF-κB nuclear translocation in Lipid A-stimulated human PBMDMs. (A) PBMC-derived macrophages from human subjects were transduced with a fluorescent lentiviral p65AmCyan construct and were used to image NF-κB p65 subunit cellular dynamics in real-time. (B) <t>CellTracker</t> was used to generate profiles of nuclear translocation of transduced cells post stimulation with 200ng/mL Lipid A, over 3h: Asterisks (*) indicate nuclear localization of p65 at 66 and 93 min (‘). (C-E) Graphs of individual nuclear translocation profiles of responding cells in the healthy controls, Crohn’s disease (CD) and ulcerative colitis (UC) groups; mean ± SD for all responsive cells shown in blue, red and green colour lines for each group, respectively. (F) The proportion of responding cells was calculated by pooling all tracked cells from each disease group; *p<0.05; two-sided Fisher’s exact test (by summation). Peak identification and analysis revealed in each population the peak time (G), peak amplitude (H) and peak width (I): *p<0.05, ***p<0.001; statistical differences assessed by Kruskal Wallis test with pairwise comparison of all three groups.
    Based Software Celltracker, supplied by MathWorks 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/based software celltracker/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    based software celltracker - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    ( A ) The top view and side view of REF 2c labeled with CellTracker-Green dye at 24 hr and 48 hr. Scale bar, 100 μm. ( B ) Zoomed side view of REF 2c labeled with CellTracker-Green dye at 24 hr and 48 hr. Scale bar, 10 μm. ( C ) Bar plot showing the tissue thickness at 24 hr ( n = 12) and 48 hr ( n = 12). **, p < 0.01. ( D ) Plot showing the mean thickness across the REF colony at 24 hr ( n = 12) and 48 hr ( n = 12).

    Journal: eLife

    Article Title: Condensation tendency and planar isotropic actin gradient induce radial alignment in confined monolayers

    doi: 10.7554/eLife.60381

    Figure Lengend Snippet: ( A ) The top view and side view of REF 2c labeled with CellTracker-Green dye at 24 hr and 48 hr. Scale bar, 100 μm. ( B ) Zoomed side view of REF 2c labeled with CellTracker-Green dye at 24 hr and 48 hr. Scale bar, 10 μm. ( C ) Bar plot showing the tissue thickness at 24 hr ( n = 12) and 48 hr ( n = 12). **, p < 0.01. ( D ) Plot showing the mean thickness across the REF colony at 24 hr ( n = 12) and 48 hr ( n = 12).

    Article Snippet: To analyze cell migration, individual cell positions were manually tracked using CellTracker software ( ) implemented in MATLAB (MATLAB R2020a, MathWorks).

    Techniques: Labeling

    Time-lapse Confocal imaging of NF-κB nuclear translocation in Lipid A-stimulated human PBMDMs. (A) PBMC-derived macrophages from human subjects were transduced with a fluorescent lentiviral p65AmCyan construct and were used to image NF-κB p65 subunit cellular dynamics in real-time. (B) CellTracker was used to generate profiles of nuclear translocation of transduced cells post stimulation with 200ng/mL Lipid A, over 3h: Asterisks (*) indicate nuclear localization of p65 at 66 and 93 min (‘). (C-E) Graphs of individual nuclear translocation profiles of responding cells in the healthy controls, Crohn’s disease (CD) and ulcerative colitis (UC) groups; mean ± SD for all responsive cells shown in blue, red and green colour lines for each group, respectively. (F) The proportion of responding cells was calculated by pooling all tracked cells from each disease group; *p<0.05; two-sided Fisher’s exact test (by summation). Peak identification and analysis revealed in each population the peak time (G), peak amplitude (H) and peak width (I): *p<0.05, ***p<0.001; statistical differences assessed by Kruskal Wallis test with pairwise comparison of all three groups.

    Journal: bioRxiv

    Article Title: Macrophage-specific NF-κB activation dynamics can segregate inflammatory bowel disease patients

    doi: 10.1101/535096

    Figure Lengend Snippet: Time-lapse Confocal imaging of NF-κB nuclear translocation in Lipid A-stimulated human PBMDMs. (A) PBMC-derived macrophages from human subjects were transduced with a fluorescent lentiviral p65AmCyan construct and were used to image NF-κB p65 subunit cellular dynamics in real-time. (B) CellTracker was used to generate profiles of nuclear translocation of transduced cells post stimulation with 200ng/mL Lipid A, over 3h: Asterisks (*) indicate nuclear localization of p65 at 66 and 93 min (‘). (C-E) Graphs of individual nuclear translocation profiles of responding cells in the healthy controls, Crohn’s disease (CD) and ulcerative colitis (UC) groups; mean ± SD for all responsive cells shown in blue, red and green colour lines for each group, respectively. (F) The proportion of responding cells was calculated by pooling all tracked cells from each disease group; *p<0.05; two-sided Fisher’s exact test (by summation). Peak identification and analysis revealed in each population the peak time (G), peak amplitude (H) and peak width (I): *p<0.05, ***p<0.001; statistical differences assessed by Kruskal Wallis test with pairwise comparison of all three groups.

    Article Snippet: Cells were imaged using a Zeiss LSM880 confocal microscope system equipped with a cell incubation unit maintained at 37 ° C, in a humidified atmosphere of 5% CO 2 . p65-AmCyan nuclear fluorescence was detected (excitation λ 458nm, emission λ 489nm) and quantified using CellTracker software ( ).

    Techniques: Imaging, Translocation Assay, Derivative Assay, Transduction, Construct, Comparison