infinity capture 6.3.0 software Search Results


ucb 6 3 0 6 6 3 0 6 96 63 0 24 ts 4 8  (Enamine Ltd)
90
Enamine Ltd ucb 6 3 0 6 6 3 0 6 96 63 0 24 ts 4 8
Ucb 6 3 0 6 6 3 0 6 96 63 0 24 Ts 4 8, supplied by Enamine 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/ucb 6 3 0 6 6 3 0 6 96 63 0 24 ts 4 8/product/Enamine Ltd
Average 90 stars, based on 1 article reviews
ucb 6 3 0 6 6 3 0 6 96 63 0 24 ts 4 8 - by Bioz Stars, 2026-05
90/100 stars
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zen software  (Carl Zeiss)
99
Carl Zeiss zen software
Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× <t>magnification.</t> <t>Software</t> to analyze signal co-localization was <t>ZEN-2010</t> (see ).
Zen Software, supplied by Carl Zeiss, 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/zen software/product/Carl Zeiss
Average 99 stars, based on 1 article reviews
zen software - by Bioz Stars, 2026-05
99/100 stars
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axiovision software  (Carl Zeiss)
90
Carl Zeiss axiovision software
Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× <t>magnification.</t> <t>Software</t> to analyze signal co-localization was <t>ZEN-2010</t> (see ).
Axiovision 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/axiovision software/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
axiovision software - by Bioz Stars, 2026-05
90/100 stars
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compass simple western software  (Protein Simple Inc)
99
Protein Simple Inc compass simple western software
Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× <t>magnification.</t> <t>Software</t> to analyze signal co-localization was <t>ZEN-2010</t> (see ).
Compass Simple Western Software, supplied by Protein Simple Inc, 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/compass simple western software/product/Protein Simple Inc
Average 99 stars, based on 1 article reviews
compass simple western software - by Bioz Stars, 2026-05
99/100 stars
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image capture software zeiss axiovision 4.6.3.0  (Carl Zeiss)
90
Carl Zeiss image capture software zeiss axiovision 4.6.3.0
Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× <t>magnification.</t> <t>Software</t> to analyze signal co-localization was <t>ZEN-2010</t> (see ).
Image Capture Software Zeiss Axiovision 4.6.3.0, 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/image capture software zeiss axiovision 4.6.3.0/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
image capture software zeiss axiovision 4.6.3.0 - by Bioz Stars, 2026-05
90/100 stars
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image processing software axiovision v 4.6.3.0  (Carl Zeiss)
90
Carl Zeiss image processing software axiovision v 4.6.3.0
Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× <t>magnification.</t> <t>Software</t> to analyze signal co-localization was <t>ZEN-2010</t> (see ).
Image Processing Software Axiovision V 4.6.3.0, 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/image processing software axiovision v 4.6.3.0/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
image processing software axiovision v 4.6.3.0 - by Bioz Stars, 2026-05
90/100 stars
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fa 45 630 rotor  (Eppendorf AG)
96
Eppendorf AG fa 45 630 rotor
Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× <t>magnification.</t> <t>Software</t> to analyze signal co-localization was <t>ZEN-2010</t> (see ).
Fa 45 630 Rotor, supplied by Eppendorf AG, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/fa 45 630 rotor/product/Eppendorf AG
Average 96 stars, based on 1 article reviews
fa 45 630 rotor - by Bioz Stars, 2026-05
96/100 stars
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feso 4 • 7h 2 o 7782-63-0  (Merck KGaA)
90
Merck KGaA feso 4 • 7h 2 o 7782-63-0
Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× <t>magnification.</t> <t>Software</t> to analyze signal co-localization was <t>ZEN-2010</t> (see ).
Feso 4 • 7h 2 O 7782 63 0, supplied by Merck KGaA, 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/feso 4 • 7h 2 o 7782-63-0/product/Merck KGaA
Average 90 stars, based on 1 article reviews
feso 4 • 7h 2 o 7782-63-0 - by Bioz Stars, 2026-05
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interproscan v5.24-63.0  (InterPro Inc)
90
InterPro Inc interproscan v5.24-63.0
Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× <t>magnification.</t> <t>Software</t> to analyze signal co-localization was <t>ZEN-2010</t> (see ).
Interproscan V5.24 63.0, supplied by InterPro 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/interproscan v5.24-63.0/product/InterPro Inc
Average 90 stars, based on 1 article reviews
interproscan v5.24-63.0 - by Bioz Stars, 2026-05
90/100 stars
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jchem 6.3.0  (ChemAxon LLC)
90
ChemAxon LLC jchem 6.3.0
Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× <t>magnification.</t> <t>Software</t> to analyze signal co-localization was <t>ZEN-2010</t> (see ).
Jchem 6.3.0, supplied by ChemAxon LLC, 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/jchem 6.3.0/product/ChemAxon LLC
Average 90 stars, based on 1 article reviews
jchem 6.3.0 - by Bioz Stars, 2026-05
90/100 stars
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achroplan 63 ×/0.80 lens  (Carl Zeiss)
90
Carl Zeiss achroplan 63 ×/0.80 lens
Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× <t>magnification.</t> <t>Software</t> to analyze signal co-localization was <t>ZEN-2010</t> (see ).
Achroplan 63 ×/0.80 Lens, 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/achroplan 63 ×/0.80 lens/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
achroplan 63 ×/0.80 lens - by Bioz Stars, 2026-05
90/100 stars
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interpro version 63.0  (InterPro Inc)
90
InterPro Inc interpro version 63.0
Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× <t>magnification.</t> <t>Software</t> to analyze signal co-localization was <t>ZEN-2010</t> (see ).
Interpro Version 63.0, supplied by InterPro 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/interpro version 63.0/product/InterPro Inc
Average 90 stars, based on 1 article reviews
interpro version 63.0 - by Bioz Stars, 2026-05
90/100 stars
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Image Search Results


Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× magnification. Software to analyze signal co-localization was ZEN-2010 (see ).

Journal: International Journal of Molecular Sciences

Article Title: Cell Cycle Reactivation, at the Start of Neurodegeneration, Induced by Forskolin and Aniline in Differentiated Neuroblastoma Cells

doi: 10.3390/ijms241814373

Figure Lengend Snippet: Dual color immunolocalization of tau epitopes in SH-SY5Y cells. ( A – C ) Replicative SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. ( D – F ) Differentiated SH-SY5Y cells with the visualization of Tau-1, Tau-5, and AT8 epitopes, respectively. Tau-1, Tau-5, and AT8 were revealed by FITC-conjugated antibodies (green signals). Ki-67 (replication marker) and UBTF (nucleolar marker) were detected by TRITC-conjugated antibodies (red signals). DAPI (blue signals) was used to stain cell nuclei. White arrow in ( E ) indicates a cell nucleus with the presence of the Ki-67 marker. White arrow in ( F ) indicates the co-localization of AT8 and UBTF in a nucleus. Magnification is the same for all the images, with a unique scale bar shown in ( F ): 10 μm. The images were captured by confocal laser scanning microscope at 630× magnification. Software to analyze signal co-localization was ZEN-2010 (see ).

Article Snippet: The immunodetection was analyzed using a confocal laser scanning microscopy (CLSM) (LSM700, Zeiss, Oberkochen, Baden-Württemberg, Germany) and images were captured at 400× and/or 630× magnification using the ZEN software (ZEN 2010B SP1 v. 6.0.0.485, Zeiss) for image acquisitions and analysis.

Techniques: Marker, Staining, Laser-Scanning Microscopy, Software

Example of co-localization of IIF signals in the cell nucleus. ( A ) serial section along the z-axis of a cell showing detection of tau (green signals) and ki-67 (red signals). Each image (from 1 to 15) corresponds to a serial section of 0.3 µm thickness. ( B ) Orthogonal view of the same cell shown in ( A ). In the upper part is presented a view of cell section along the green horizontal line. In the right part is presented a view of the cell section along the red vertical line. ( C ) The same cell is shown in ( A ) with the fluorescence intensity (graph on the left) of the tau (green), Ki-67 (red), and DAPI (blue) along the red line indicated by the number 1. The images show the localization in the same nuclear compartment of the analyzed epitopes. Scale bars (5 µm) were indicated for each panel ( A – C ). Images were produced with the ZEN-2010 software.

Journal: International Journal of Molecular Sciences

Article Title: Cell Cycle Reactivation, at the Start of Neurodegeneration, Induced by Forskolin and Aniline in Differentiated Neuroblastoma Cells

doi: 10.3390/ijms241814373

Figure Lengend Snippet: Example of co-localization of IIF signals in the cell nucleus. ( A ) serial section along the z-axis of a cell showing detection of tau (green signals) and ki-67 (red signals). Each image (from 1 to 15) corresponds to a serial section of 0.3 µm thickness. ( B ) Orthogonal view of the same cell shown in ( A ). In the upper part is presented a view of cell section along the green horizontal line. In the right part is presented a view of the cell section along the red vertical line. ( C ) The same cell is shown in ( A ) with the fluorescence intensity (graph on the left) of the tau (green), Ki-67 (red), and DAPI (blue) along the red line indicated by the number 1. The images show the localization in the same nuclear compartment of the analyzed epitopes. Scale bars (5 µm) were indicated for each panel ( A – C ). Images were produced with the ZEN-2010 software.

Article Snippet: The immunodetection was analyzed using a confocal laser scanning microscopy (CLSM) (LSM700, Zeiss, Oberkochen, Baden-Württemberg, Germany) and images were captured at 400× and/or 630× magnification using the ZEN software (ZEN 2010B SP1 v. 6.0.0.485, Zeiss) for image acquisitions and analysis.

Techniques: Fluorescence, Produced, Software