imagej plugin mtrackj Search Results


imaris  (Oxford Instruments)
99
Oxford Instruments imaris
Imaris, supplied by Oxford Instruments, 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/result/imaris/product/Oxford Instruments
Average 99 stars, based on 1 article reviews
imaris - by Bioz Stars, 2026-05
99/100 stars
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mtrackj plugin  (Ibidi USA)
90
Ibidi USA mtrackj plugin
Mtrackj Plugin, supplied by Ibidi USA, 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/mtrackj plugin/product/Ibidi USA
Average 90 stars, based on 1 article reviews
mtrackj plugin - by Bioz Stars, 2026-05
90/100 stars
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mtrackj plugin  (GraphPad Software Inc)
90
GraphPad Software Inc mtrackj plugin
Mtrackj Plugin, supplied by GraphPad Software 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/mtrackj plugin/product/GraphPad Software Inc
Average 90 stars, based on 1 article reviews
mtrackj plugin - by Bioz Stars, 2026-05
90/100 stars
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imagej  (Ibidi USA)
90
Ibidi USA imagej
Imagej, supplied by Ibidi USA, 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/imagej/product/Ibidi USA
Average 90 stars, based on 1 article reviews
imagej - by Bioz Stars, 2026-05
90/100 stars
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imagej  (GraphPad Software Inc)
90
GraphPad Software Inc imagej
( A ) Representative images of wt and Mfn2 -null mice embryonic <t>fibroblasts</t> <t>(MEFs)</t> stained with F-actin (phalloidin) under a 40× microscope. Scale bar: 50 µm. ( B ) FiloQuant plugin in <t>ImageJ</t> was used to identify cell edges and the actin cytoskeleton. The algorithm defines a 20-pixel stroke inside the cell border as the ‘border region’ and then calculates the percentage of the actin cytoskeleton in the border region and the cell circularity. If the circularity is higher than 0.6, and more than 50% of the actin cytoskeleton is in the border region, we consider the cell a PAB cell.
Imagej, supplied by GraphPad Software 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/imagej/product/GraphPad Software Inc
Average 90 stars, based on 1 article reviews
imagej - by Bioz Stars, 2026-05
90/100 stars
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chemotaxis tool  (Ibidi USA)
90
Ibidi USA chemotaxis tool
( A ) Representative images of wt and Mfn2 -null mice embryonic <t>fibroblasts</t> <t>(MEFs)</t> stained with F-actin (phalloidin) under a 40× microscope. Scale bar: 50 µm. ( B ) FiloQuant plugin in <t>ImageJ</t> was used to identify cell edges and the actin cytoskeleton. The algorithm defines a 20-pixel stroke inside the cell border as the ‘border region’ and then calculates the percentage of the actin cytoskeleton in the border region and the cell circularity. If the circularity is higher than 0.6, and more than 50% of the actin cytoskeleton is in the border region, we consider the cell a PAB cell.
Chemotaxis Tool, supplied by Ibidi USA, 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/chemotaxis tool/product/Ibidi USA
Average 90 stars, based on 1 article reviews
chemotaxis tool - by Bioz Stars, 2026-05
90/100 stars
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nis  (Nikon)
99
Nikon nis
( A ) Representative images of wt and Mfn2 -null mice embryonic <t>fibroblasts</t> <t>(MEFs)</t> stained with F-actin (phalloidin) under a 40× microscope. Scale bar: 50 µm. ( B ) FiloQuant plugin in <t>ImageJ</t> was used to identify cell edges and the actin cytoskeleton. The algorithm defines a 20-pixel stroke inside the cell border as the ‘border region’ and then calculates the percentage of the actin cytoskeleton in the border region and the cell circularity. If the circularity is higher than 0.6, and more than 50% of the actin cytoskeleton is in the border region, we consider the cell a PAB cell.
Nis, 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/result/nis/product/Nikon
Average 99 stars, based on 1 article reviews
nis - by Bioz Stars, 2026-05
99/100 stars
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axiovision  (Carl Zeiss)
90
Carl Zeiss axiovision
( A ) Representative images of wt and Mfn2 -null mice embryonic <t>fibroblasts</t> <t>(MEFs)</t> stained with F-actin (phalloidin) under a 40× microscope. Scale bar: 50 µm. ( B ) FiloQuant plugin in <t>ImageJ</t> was used to identify cell edges and the actin cytoskeleton. The algorithm defines a 20-pixel stroke inside the cell border as the ‘border region’ and then calculates the percentage of the actin cytoskeleton in the border region and the cell circularity. If the circularity is higher than 0.6, and more than 50% of the actin cytoskeleton is in the border region, we consider the cell a PAB cell.
Axiovision, 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/axiovision/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
axiovision - by Bioz Stars, 2026-05
90/100 stars
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axiovert 135tv microscope  (Carl Zeiss)
90
Carl Zeiss axiovert 135tv microscope
( A ) Representative images of wt and Mfn2 -null mice embryonic <t>fibroblasts</t> <t>(MEFs)</t> stained with F-actin (phalloidin) under a 40× microscope. Scale bar: 50 µm. ( B ) FiloQuant plugin in <t>ImageJ</t> was used to identify cell edges and the actin cytoskeleton. The algorithm defines a 20-pixel stroke inside the cell border as the ‘border region’ and then calculates the percentage of the actin cytoskeleton in the border region and the cell circularity. If the circularity is higher than 0.6, and more than 50% of the actin cytoskeleton is in the border region, we consider the cell a PAB cell.
Axiovert 135tv Microscope, 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/axiovert 135tv microscope/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
axiovert 135tv microscope - by Bioz Stars, 2026-05
90/100 stars
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cell counter  (MetaMorph Inc)
90
MetaMorph Inc cell counter
( A ) Representative images of wt and Mfn2 -null mice embryonic <t>fibroblasts</t> <t>(MEFs)</t> stained with F-actin (phalloidin) under a 40× microscope. Scale bar: 50 µm. ( B ) FiloQuant plugin in <t>ImageJ</t> was used to identify cell edges and the actin cytoskeleton. The algorithm defines a 20-pixel stroke inside the cell border as the ‘border region’ and then calculates the percentage of the actin cytoskeleton in the border region and the cell circularity. If the circularity is higher than 0.6, and more than 50% of the actin cytoskeleton is in the border region, we consider the cell a PAB cell.
Cell Counter, supplied by MetaMorph 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/cell counter/product/MetaMorph Inc
Average 90 stars, based on 1 article reviews
cell counter - by Bioz Stars, 2026-05
90/100 stars
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nikon tie fluorescent microscope  (Nikon)
99
Nikon nikon tie fluorescent microscope
( A ) Representative images of wt and Mfn2 -null mice embryonic <t>fibroblasts</t> <t>(MEFs)</t> stained with F-actin (phalloidin) under a 40× microscope. Scale bar: 50 µm. ( B ) FiloQuant plugin in <t>ImageJ</t> was used to identify cell edges and the actin cytoskeleton. The algorithm defines a 20-pixel stroke inside the cell border as the ‘border region’ and then calculates the percentage of the actin cytoskeleton in the border region and the cell circularity. If the circularity is higher than 0.6, and more than 50% of the actin cytoskeleton is in the border region, we consider the cell a PAB cell.
Nikon Tie Fluorescent Microscope, 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/result/nikon tie fluorescent microscope/product/Nikon
Average 99 stars, based on 1 article reviews
nikon tie fluorescent microscope - by Bioz Stars, 2026-05
99/100 stars
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prism 6.0  (GraphPad Software Inc)
90
GraphPad Software Inc prism 6.0
( A ) Representative images of wt and Mfn2 -null mice embryonic <t>fibroblasts</t> <t>(MEFs)</t> stained with F-actin (phalloidin) under a 40× microscope. Scale bar: 50 µm. ( B ) FiloQuant plugin in <t>ImageJ</t> was used to identify cell edges and the actin cytoskeleton. The algorithm defines a 20-pixel stroke inside the cell border as the ‘border region’ and then calculates the percentage of the actin cytoskeleton in the border region and the cell circularity. If the circularity is higher than 0.6, and more than 50% of the actin cytoskeleton is in the border region, we consider the cell a PAB cell.
Prism 6.0, supplied by GraphPad Software 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/prism 6.0/product/GraphPad Software Inc
Average 90 stars, based on 1 article reviews
prism 6.0 - by Bioz Stars, 2026-05
90/100 stars
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Image Search Results


( A ) Representative images of wt and Mfn2 -null mice embryonic fibroblasts (MEFs) stained with F-actin (phalloidin) under a 40× microscope. Scale bar: 50 µm. ( B ) FiloQuant plugin in ImageJ was used to identify cell edges and the actin cytoskeleton. The algorithm defines a 20-pixel stroke inside the cell border as the ‘border region’ and then calculates the percentage of the actin cytoskeleton in the border region and the cell circularity. If the circularity is higher than 0.6, and more than 50% of the actin cytoskeleton is in the border region, we consider the cell a PAB cell.

Journal: eLife

Article Title: Atypical peripheral actin band formation via overactivation of RhoA and nonmuscle myosin II in mitofusin 2-deficient cells

doi: 10.7554/eLife.88828

Figure Lengend Snippet: ( A ) Representative images of wt and Mfn2 -null mice embryonic fibroblasts (MEFs) stained with F-actin (phalloidin) under a 40× microscope. Scale bar: 50 µm. ( B ) FiloQuant plugin in ImageJ was used to identify cell edges and the actin cytoskeleton. The algorithm defines a 20-pixel stroke inside the cell border as the ‘border region’ and then calculates the percentage of the actin cytoskeleton in the border region and the cell circularity. If the circularity is higher than 0.6, and more than 50% of the actin cytoskeleton is in the border region, we consider the cell a PAB cell.

Article Snippet: The velocity of MEFs was measured using ImageJ with the MTrackJ plugin and plotted in Prism 6.0 (GraphPad).

Techniques: Staining, Microscopy

Journal: eLife

Article Title: Atypical peripheral actin band formation via overactivation of RhoA and nonmuscle myosin II in mitofusin 2-deficient cells

doi: 10.7554/eLife.88828

Figure Lengend Snippet:

Article Snippet: The velocity of MEFs was measured using ImageJ with the MTrackJ plugin and plotted in Prism 6.0 (GraphPad).

Techniques: Transfection, Construct, Over Expression, Expressing, Dominant Negative Mutation, Recombinant, Plasmid Preparation, Sequencing, Staining, Activation Assay, Imaging, Clone Assay, Software, Microscopy