data acquisition card daq model 626 Search Results


axiovert 200m  (Carl Zeiss)
96
Carl Zeiss axiovert 200m
Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated <t>Axiovert</t> 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.
Axiovert 200m, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
axiovert 200m - by Bioz Stars, 2026-05
96/100 stars
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axioscan.z1 fluorescence slide scanner  (Carl Zeiss)
90
Carl Zeiss axioscan.z1 fluorescence slide scanner
Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated <t>Axiovert</t> 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.
Axioscan.Z1 Fluorescence Slide Scanner, 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/axioscan.z1 fluorescence slide scanner/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
axioscan.z1 fluorescence slide scanner - by Bioz Stars, 2026-05
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zen blue 2012 software  (Carl Zeiss)
90
Carl Zeiss zen blue 2012 software
Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated <t>Axiovert</t> 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.
Zen Blue 2012 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/zen blue 2012 software/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
zen blue 2012 software - by Bioz Stars, 2026-05
90/100 stars
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libra 120 plus tem  (Carl Zeiss)
90
Carl Zeiss libra 120 plus tem
Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated <t>Axiovert</t> 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.
Libra 120 Plus Tem, 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/libra 120 plus tem/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
libra 120 plus tem - by Bioz Stars, 2026-05
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lsm 510 software  (Carl Zeiss)
90
Carl Zeiss lsm 510 software
Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated <t>Axiovert</t> 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.
Lsm 510 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/lsm 510 software/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
lsm 510 software - by Bioz Stars, 2026-05
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zen blue (zeiss lsm 800 confocal microscope image acquisition)  (Carl Zeiss)
90
Carl Zeiss zen blue (zeiss lsm 800 confocal microscope image acquisition)
Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated <t>Axiovert</t> 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.
Zen Blue (Zeiss Lsm 800 Confocal Microscope Image Acquisition), 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/zen blue (zeiss lsm 800 confocal microscope image acquisition)/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
zen blue (zeiss lsm 800 confocal microscope image acquisition) - by Bioz Stars, 2026-05
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zeiss imager.a2 microscope  (Carl Zeiss)
90
Carl Zeiss zeiss imager.a2 microscope
Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated <t>Axiovert</t> 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.
Zeiss Imager.A2 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/zeiss imager.a2 microscope/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
zeiss imager.a2 microscope - by Bioz Stars, 2026-05
90/100 stars
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multifunction data acquisition card  (Advantech)
86
Advantech multifunction data acquisition card
Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated <t>Axiovert</t> 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.
Multifunction Data Acquisition Card, supplied by Advantech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
multifunction data acquisition card - by Bioz Stars, 2026-05
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chrom card trace focus gc software  (Chrom Tech)
86
Chrom Tech chrom card trace focus gc software
Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated <t>Axiovert</t> 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.
Chrom Card Trace Focus Gc Software, supplied by Chrom Tech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
chrom card trace focus gc software - by Bioz Stars, 2026-05
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4/20 data recording system  (POWERLAB INC)
90
POWERLAB INC 4/20 data recording system
Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated <t>Axiovert</t> 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.
4/20 Data Recording System, supplied by POWERLAB 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/4/20 data recording system/product/POWERLAB INC
Average 90 stars, based on 1 article reviews
4/20 data recording system - by Bioz Stars, 2026-05
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spc 850 data acquisition card  (Becker & Hickl)
90
Becker & Hickl spc 850 data acquisition card
Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated <t>Axiovert</t> 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.
Spc 850 Data Acquisition Card, supplied by Becker & Hickl, 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/spc 850 data acquisition card/product/Becker & Hickl
Average 90 stars, based on 1 article reviews
spc 850 data acquisition card - by Bioz Stars, 2026-05
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data card sensoray model 626  (Sensoray Co Inc)
90
Sensoray Co Inc data card sensoray model 626
Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated <t>Axiovert</t> 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.
Data Card Sensoray Model 626, supplied by Sensoray Co 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/data card sensoray model 626/product/Sensoray Co Inc
Average 90 stars, based on 1 article reviews
data card sensoray model 626 - by Bioz Stars, 2026-05
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Image Search Results


Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated Axiovert 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.

Journal: Molecules

Article Title: A Secreted Phospholipase A 2 Induces Formation of Smooth Muscle Foam Cells Which Transdifferentiate to Macrophage-Like State

doi: 10.3390/molecules24183244

Figure Lengend Snippet: Phagocytotic activity and upregulation of macrophage markers in VSMCs induced by MT-III. VSMCs (2.5 × 10 3 cells/well) were treated with MT-III (0.4 and 0.8 μM) or DMEM (Control) for 12, 24, and 48 h, followed by incubation with 0.5 μm fluorescent beads (red) for 6 h. Cells were then washed extensively, fixed with paraformaldehyde (4%), counterstained with Hoechst 33342 (blue-nuclei), and analyzed with an automated Axiovert 200 m followed by a computerized automatic quantification in the CellProfiler analysis software. ( A ) The number of latex beads per cell was counted to obtain numerical data for the total phagocytotic activity. ( B ) A representative field of view. ( C ) The effect of MT-III on VSMC and macrophage-related gene expression in rat VSMCs. Subconfluent rat VSMCs (8 × 10 5 cells/well) were treated with MT-III (0.4 and 0.8 μM) or with DMEM medium (control) for 48 h. Total RNA was extracted and subjected to RT-PCR analysis. Values represent the mean ± SEM from six animals ( n = 6) (ANOVA). Note: * p < 0.05 compared with control cells.

Article Snippet: Data acquisition was accomplished with automated Axiovert 200m (Carl Zeiss MicroImaging GmbH, Jena, Germany) followed by a computerized automatic quantification in the CellProfiler analysis software.

Techniques: Activity Assay, Incubation, Software, Expressing, Reverse Transcription Polymerase Chain Reaction