automated particle detection software (utrack) Search Results


particle tracking software utrack 2.0  (MathWorks Inc)
90
MathWorks Inc particle tracking software utrack 2.0
Particle Tracking Software Utrack 2.0, 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
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particle tracking software utrack 2.0 - by Bioz Stars, 2026-03
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automated particle detection software utrack  (MathWorks Inc)
90
MathWorks Inc automated particle detection software utrack
Automated Particle Detection Software Utrack, 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/automated particle detection software utrack/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
automated particle detection software utrack - by Bioz Stars, 2026-03
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utrack  (MathWorks Inc)
90
MathWorks Inc utrack
Utrack, 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/utrack/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
utrack - by Bioz Stars, 2026-03
90/100 stars
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modified matlab code based on utrack  (MathWorks Inc)
90
MathWorks Inc modified matlab code based on utrack
Modified Matlab Code Based On Utrack, 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/modified matlab code based on utrack/product/MathWorks Inc
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modified matlab code based on utrack - by Bioz Stars, 2026-03
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utrack algorithm  (MathWorks Inc)
90
MathWorks Inc utrack algorithm
Utrack Algorithm, 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/utrack algorithm/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
utrack algorithm - by Bioz Stars, 2026-03
90/100 stars
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utrack analysis program  (MathWorks Inc)
90
MathWorks Inc utrack analysis program
( A ) Representative phenotypes of EB3 localization in control and CKAP5 -silenced groups. NAR cells were transiently transfected with EB3.eGFP plasmid to label the microtubule + ends. After 12 hours of transfection, cells were further transfected with siControl/si CKAP5 LNPs, and live-cell imaging was performed after 30 hours of siRNA-mediated silencing. Live cell imaging was performed by a superresolution spinning disk microscope. Images were captured at 100×. Scale bars, 5 μm. Images were captured every second for a period of 90 s. The images represent superimposition images of 91 frames with each frame marked in a specific shade as shown in the time frame scale. Nondynamic + ends superimpose on each other in all 90 frames due to their static nature and represent as white due to superimposition, whereas dynamic + ends do not superimpose in all the 90 frames due to their dynamic behavior and thus appear as a rainbow color. Thus, higher dynamics of tubulin result in a wider range of colors in these representative superimposed images. ( B ) Quantitative representation of the microtubule (MT) growth speed in control and CKAP5 -silenced group. The live-cell kinetic data obtained from a spinning disk microscope was subjected to <t>Utrack</t> analysis <t>using</t> <t>MATLAB</t> software. ** P = 0.0097. ( C ) Quantitative representation of the MT growth lifetime in control- and CKAP5 -silenced group as measured by MATLAB analysis. ( D ) Quantitative representation of the MT growth length in control and CKAP5 -silenced group as measured by MATLAB analysis. For all the graphical analysis in (B) to (D), the data are represented as mean ± SEM from 10 mitotic events and statistically analyzed by an unpaired t test.
Utrack Analysis Program, 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/utrack analysis program/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
utrack analysis program - by Bioz Stars, 2026-03
90/100 stars
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utrack matlab analysis method  (MathWorks Inc)
90
MathWorks Inc utrack matlab analysis method
( A ) Representative phenotypes of EB3 localization in control and CKAP5 -silenced groups. NAR cells were transiently transfected with EB3.eGFP plasmid to label the microtubule + ends. After 12 hours of transfection, cells were further transfected with siControl/si CKAP5 LNPs, and live-cell imaging was performed after 30 hours of siRNA-mediated silencing. Live cell imaging was performed by a superresolution spinning disk microscope. Images were captured at 100×. Scale bars, 5 μm. Images were captured every second for a period of 90 s. The images represent superimposition images of 91 frames with each frame marked in a specific shade as shown in the time frame scale. Nondynamic + ends superimpose on each other in all 90 frames due to their static nature and represent as white due to superimposition, whereas dynamic + ends do not superimpose in all the 90 frames due to their dynamic behavior and thus appear as a rainbow color. Thus, higher dynamics of tubulin result in a wider range of colors in these representative superimposed images. ( B ) Quantitative representation of the microtubule (MT) growth speed in control and CKAP5 -silenced group. The live-cell kinetic data obtained from a spinning disk microscope was subjected to <t>Utrack</t> analysis using <t>MATLAB</t> software. ** P = 0.0097. ( C ) Quantitative representation of the MT growth lifetime in control- and CKAP5 -silenced group as measured by MATLAB analysis. ( D ) Quantitative representation of the MT growth length in control and CKAP5 -silenced group as measured by MATLAB analysis. For all the graphical analysis in (B) to (D), the data are represented as mean ± SEM from 10 mitotic events and statistically analyzed by an unpaired t test.
Utrack Matlab Analysis Method, 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/utrack matlab analysis method/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
utrack matlab analysis method - by Bioz Stars, 2026-03
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utrack package  (MathWorks Inc)
90
MathWorks Inc utrack package
( A ) Representative phenotypes of EB3 localization in control and CKAP5 -silenced groups. NAR cells were transiently transfected with EB3.eGFP plasmid to label the microtubule + ends. After 12 hours of transfection, cells were further transfected with siControl/si CKAP5 LNPs, and live-cell imaging was performed after 30 hours of siRNA-mediated silencing. Live cell imaging was performed by a superresolution spinning disk microscope. Images were captured at 100×. Scale bars, 5 μm. Images were captured every second for a period of 90 s. The images represent superimposition images of 91 frames with each frame marked in a specific shade as shown in the time frame scale. Nondynamic + ends superimpose on each other in all 90 frames due to their static nature and represent as white due to superimposition, whereas dynamic + ends do not superimpose in all the 90 frames due to their dynamic behavior and thus appear as a rainbow color. Thus, higher dynamics of tubulin result in a wider range of colors in these representative superimposed images. ( B ) Quantitative representation of the microtubule (MT) growth speed in control and CKAP5 -silenced group. The live-cell kinetic data obtained from a spinning disk microscope was subjected to <t>Utrack</t> analysis using <t>MATLAB</t> software. ** P = 0.0097. ( C ) Quantitative representation of the MT growth lifetime in control- and CKAP5 -silenced group as measured by MATLAB analysis. ( D ) Quantitative representation of the MT growth length in control and CKAP5 -silenced group as measured by MATLAB analysis. For all the graphical analysis in (B) to (D), the data are represented as mean ± SEM from 10 mitotic events and statistically analyzed by an unpaired t test.
Utrack Package, 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/utrack package/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
utrack package - by Bioz Stars, 2026-03
90/100 stars
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matlab v. 2018b  (MathWorks Inc)
90
MathWorks Inc matlab v. 2018b
( A ) Representative phenotypes of EB3 localization in control and CKAP5 -silenced groups. NAR cells were transiently transfected with EB3.eGFP plasmid to label the microtubule + ends. After 12 hours of transfection, cells were further transfected with siControl/si CKAP5 LNPs, and live-cell imaging was performed after 30 hours of siRNA-mediated silencing. Live cell imaging was performed by a superresolution spinning disk microscope. Images were captured at 100×. Scale bars, 5 μm. Images were captured every second for a period of 90 s. The images represent superimposition images of 91 frames with each frame marked in a specific shade as shown in the time frame scale. Nondynamic + ends superimpose on each other in all 90 frames due to their static nature and represent as white due to superimposition, whereas dynamic + ends do not superimpose in all the 90 frames due to their dynamic behavior and thus appear as a rainbow color. Thus, higher dynamics of tubulin result in a wider range of colors in these representative superimposed images. ( B ) Quantitative representation of the microtubule (MT) growth speed in control and CKAP5 -silenced group. The live-cell kinetic data obtained from a spinning disk microscope was subjected to <t>Utrack</t> analysis using <t>MATLAB</t> software. ** P = 0.0097. ( C ) Quantitative representation of the MT growth lifetime in control- and CKAP5 -silenced group as measured by MATLAB analysis. ( D ) Quantitative representation of the MT growth length in control and CKAP5 -silenced group as measured by MATLAB analysis. For all the graphical analysis in (B) to (D), the data are represented as mean ± SEM from 10 mitotic events and statistically analyzed by an unpaired t test.
Matlab V. 2018b, 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/matlab v. 2018b/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
matlab v. 2018b - by Bioz Stars, 2026-03
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utrack 2.1.0  (MathWorks Inc)
90
MathWorks Inc utrack 2.1.0
( A ) Representative phenotypes of EB3 localization in control and CKAP5 -silenced groups. NAR cells were transiently transfected with EB3.eGFP plasmid to label the microtubule + ends. After 12 hours of transfection, cells were further transfected with siControl/si CKAP5 LNPs, and live-cell imaging was performed after 30 hours of siRNA-mediated silencing. Live cell imaging was performed by a superresolution spinning disk microscope. Images were captured at 100×. Scale bars, 5 μm. Images were captured every second for a period of 90 s. The images represent superimposition images of 91 frames with each frame marked in a specific shade as shown in the time frame scale. Nondynamic + ends superimpose on each other in all 90 frames due to their static nature and represent as white due to superimposition, whereas dynamic + ends do not superimpose in all the 90 frames due to their dynamic behavior and thus appear as a rainbow color. Thus, higher dynamics of tubulin result in a wider range of colors in these representative superimposed images. ( B ) Quantitative representation of the microtubule (MT) growth speed in control and CKAP5 -silenced group. The live-cell kinetic data obtained from a spinning disk microscope was subjected to <t>Utrack</t> analysis using <t>MATLAB</t> software. ** P = 0.0097. ( C ) Quantitative representation of the MT growth lifetime in control- and CKAP5 -silenced group as measured by MATLAB analysis. ( D ) Quantitative representation of the MT growth length in control and CKAP5 -silenced group as measured by MATLAB analysis. For all the graphical analysis in (B) to (D), the data are represented as mean ± SEM from 10 mitotic events and statistically analyzed by an unpaired t test.
Utrack 2.1.0, 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/utrack 2.1.0/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
utrack 2.1.0 - by Bioz Stars, 2026-03
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utract ugn-101  (Urogen Pharma)
90
Urogen Pharma utract ugn-101
( A ) Representative phenotypes of EB3 localization in control and CKAP5 -silenced groups. NAR cells were transiently transfected with EB3.eGFP plasmid to label the microtubule + ends. After 12 hours of transfection, cells were further transfected with siControl/si CKAP5 LNPs, and live-cell imaging was performed after 30 hours of siRNA-mediated silencing. Live cell imaging was performed by a superresolution spinning disk microscope. Images were captured at 100×. Scale bars, 5 μm. Images were captured every second for a period of 90 s. The images represent superimposition images of 91 frames with each frame marked in a specific shade as shown in the time frame scale. Nondynamic + ends superimpose on each other in all 90 frames due to their static nature and represent as white due to superimposition, whereas dynamic + ends do not superimpose in all the 90 frames due to their dynamic behavior and thus appear as a rainbow color. Thus, higher dynamics of tubulin result in a wider range of colors in these representative superimposed images. ( B ) Quantitative representation of the microtubule (MT) growth speed in control and CKAP5 -silenced group. The live-cell kinetic data obtained from a spinning disk microscope was subjected to <t>Utrack</t> analysis using <t>MATLAB</t> software. ** P = 0.0097. ( C ) Quantitative representation of the MT growth lifetime in control- and CKAP5 -silenced group as measured by MATLAB analysis. ( D ) Quantitative representation of the MT growth length in control and CKAP5 -silenced group as measured by MATLAB analysis. For all the graphical analysis in (B) to (D), the data are represented as mean ± SEM from 10 mitotic events and statistically analyzed by an unpaired t test.
Utract Ugn 101, supplied by Urogen Pharma, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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utract ugn-101 - by Bioz Stars, 2026-03
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Image Search Results


( A ) Representative phenotypes of EB3 localization in control and CKAP5 -silenced groups. NAR cells were transiently transfected with EB3.eGFP plasmid to label the microtubule + ends. After 12 hours of transfection, cells were further transfected with siControl/si CKAP5 LNPs, and live-cell imaging was performed after 30 hours of siRNA-mediated silencing. Live cell imaging was performed by a superresolution spinning disk microscope. Images were captured at 100×. Scale bars, 5 μm. Images were captured every second for a period of 90 s. The images represent superimposition images of 91 frames with each frame marked in a specific shade as shown in the time frame scale. Nondynamic + ends superimpose on each other in all 90 frames due to their static nature and represent as white due to superimposition, whereas dynamic + ends do not superimpose in all the 90 frames due to their dynamic behavior and thus appear as a rainbow color. Thus, higher dynamics of tubulin result in a wider range of colors in these representative superimposed images. ( B ) Quantitative representation of the microtubule (MT) growth speed in control and CKAP5 -silenced group. The live-cell kinetic data obtained from a spinning disk microscope was subjected to Utrack analysis using MATLAB software. ** P = 0.0097. ( C ) Quantitative representation of the MT growth lifetime in control- and CKAP5 -silenced group as measured by MATLAB analysis. ( D ) Quantitative representation of the MT growth length in control and CKAP5 -silenced group as measured by MATLAB analysis. For all the graphical analysis in (B) to (D), the data are represented as mean ± SEM from 10 mitotic events and statistically analyzed by an unpaired t test.

Journal: Science Advances

Article Title: Therapeutic gene silencing of CKAP5 leads to lethality in genetically unstable cancer cells

doi: 10.1126/sciadv.ade4800

Figure Lengend Snippet: ( A ) Representative phenotypes of EB3 localization in control and CKAP5 -silenced groups. NAR cells were transiently transfected with EB3.eGFP plasmid to label the microtubule + ends. After 12 hours of transfection, cells were further transfected with siControl/si CKAP5 LNPs, and live-cell imaging was performed after 30 hours of siRNA-mediated silencing. Live cell imaging was performed by a superresolution spinning disk microscope. Images were captured at 100×. Scale bars, 5 μm. Images were captured every second for a period of 90 s. The images represent superimposition images of 91 frames with each frame marked in a specific shade as shown in the time frame scale. Nondynamic + ends superimpose on each other in all 90 frames due to their static nature and represent as white due to superimposition, whereas dynamic + ends do not superimpose in all the 90 frames due to their dynamic behavior and thus appear as a rainbow color. Thus, higher dynamics of tubulin result in a wider range of colors in these representative superimposed images. ( B ) Quantitative representation of the microtubule (MT) growth speed in control and CKAP5 -silenced group. The live-cell kinetic data obtained from a spinning disk microscope was subjected to Utrack analysis using MATLAB software. ** P = 0.0097. ( C ) Quantitative representation of the MT growth lifetime in control- and CKAP5 -silenced group as measured by MATLAB analysis. ( D ) Quantitative representation of the MT growth length in control and CKAP5 -silenced group as measured by MATLAB analysis. For all the graphical analysis in (B) to (D), the data are represented as mean ± SEM from 10 mitotic events and statistically analyzed by an unpaired t test.

Article Snippet: Application of the Utrack analysis program of the MATLAB to measure the dynamics as well as lifetime of EB3 comets clearly showed a significant reduction in the microtubule growth rate in the CKAP5 -silenced group (1.6-fold reduction, P value 0.0097) ( ).

Techniques: Control, Transfection, Plasmid Preparation, Live Cell Imaging, Microscopy, Software

( A ) Representative phenotypes of EB3 localization in control and CKAP5 -silenced groups. NAR cells were transiently transfected with EB3.eGFP plasmid to label the microtubule + ends. After 12 hours of transfection, cells were further transfected with siControl/si CKAP5 LNPs, and live-cell imaging was performed after 30 hours of siRNA-mediated silencing. Live cell imaging was performed by a superresolution spinning disk microscope. Images were captured at 100×. Scale bars, 5 μm. Images were captured every second for a period of 90 s. The images represent superimposition images of 91 frames with each frame marked in a specific shade as shown in the time frame scale. Nondynamic + ends superimpose on each other in all 90 frames due to their static nature and represent as white due to superimposition, whereas dynamic + ends do not superimpose in all the 90 frames due to their dynamic behavior and thus appear as a rainbow color. Thus, higher dynamics of tubulin result in a wider range of colors in these representative superimposed images. ( B ) Quantitative representation of the microtubule (MT) growth speed in control and CKAP5 -silenced group. The live-cell kinetic data obtained from a spinning disk microscope was subjected to Utrack analysis using MATLAB software. ** P = 0.0097. ( C ) Quantitative representation of the MT growth lifetime in control- and CKAP5 -silenced group as measured by MATLAB analysis. ( D ) Quantitative representation of the MT growth length in control and CKAP5 -silenced group as measured by MATLAB analysis. For all the graphical analysis in (B) to (D), the data are represented as mean ± SEM from 10 mitotic events and statistically analyzed by an unpaired t test.

Journal: Science Advances

Article Title: Therapeutic gene silencing of CKAP5 leads to lethality in genetically unstable cancer cells

doi: 10.1126/sciadv.ade4800

Figure Lengend Snippet: ( A ) Representative phenotypes of EB3 localization in control and CKAP5 -silenced groups. NAR cells were transiently transfected with EB3.eGFP plasmid to label the microtubule + ends. After 12 hours of transfection, cells were further transfected with siControl/si CKAP5 LNPs, and live-cell imaging was performed after 30 hours of siRNA-mediated silencing. Live cell imaging was performed by a superresolution spinning disk microscope. Images were captured at 100×. Scale bars, 5 μm. Images were captured every second for a period of 90 s. The images represent superimposition images of 91 frames with each frame marked in a specific shade as shown in the time frame scale. Nondynamic + ends superimpose on each other in all 90 frames due to their static nature and represent as white due to superimposition, whereas dynamic + ends do not superimpose in all the 90 frames due to their dynamic behavior and thus appear as a rainbow color. Thus, higher dynamics of tubulin result in a wider range of colors in these representative superimposed images. ( B ) Quantitative representation of the microtubule (MT) growth speed in control and CKAP5 -silenced group. The live-cell kinetic data obtained from a spinning disk microscope was subjected to Utrack analysis using MATLAB software. ** P = 0.0097. ( C ) Quantitative representation of the MT growth lifetime in control- and CKAP5 -silenced group as measured by MATLAB analysis. ( D ) Quantitative representation of the MT growth length in control and CKAP5 -silenced group as measured by MATLAB analysis. For all the graphical analysis in (B) to (D), the data are represented as mean ± SEM from 10 mitotic events and statistically analyzed by an unpaired t test.

Article Snippet: EB3 dynamics was quantified by using the utrack MATLAB analysis method as mentioned in the protocol.

Techniques: Control, Transfection, Plasmid Preparation, Live Cell Imaging, Microscopy, Software