v. 2010b Search Results


matlab v.2010b  (MathWorks Inc)
90
MathWorks Inc matlab v.2010b
Matlab V.2010b, 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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zen v.2010b software  (Carl Zeiss)
90
Carl Zeiss zen v.2010b software
Zen V.2010b 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
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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
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matlab v. 2010b  (MathWorks Inc)
90
MathWorks Inc matlab v. 2010b
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 ).
Matlab V. 2010b, 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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zen 2010 b sp1 v.1.0.4444.17796  (Carl Zeiss)
90
Carl Zeiss zen 2010 b sp1 v.1.0.4444.17796
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 2010 B Sp1 V.1.0.4444.17796, 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
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v. 2010b  (MathWorks Inc)
90
MathWorks Inc v. 2010b
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 ).
V. 2010b, 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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fault tolerant control design for hybrid systems  (Verlag GmbH)
90
Verlag GmbH fault tolerant control design for hybrid systems
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 ).
Fault Tolerant Control Design For Hybrid Systems, supplied by Verlag GmbH, 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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© springer-verlag 2010  (Verlag GmbH)
90
Verlag GmbH © springer-verlag 2010
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 ).
© Springer Verlag 2010, supplied by Verlag GmbH, 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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matlab v. 7.11.2010b  (MathWorks Inc)
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MathWorks Inc matlab v. 7.11.2010b
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 ).
Matlab V. 7.11.2010b, 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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bsa  (CH Instruments)
90
CH Instruments bsa
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 ).
Bsa, supplied by CH Instruments, 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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human metapneumovirus strain hmpv homo sapiens per cfi0466 2010 b glycoprotein g protein  (Sino Biological)
N/A
A DNA sequence encoding the Human metapneumovirus strain HMPV Homo sapiens PER CFI0466 2010 B glycoprotein G AHV79646 1 Asp52 Ser238 was expressed with a polyhistidine tag at the C terminus
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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