3d scans Search Results


3d scanning  (Carl Zeiss)
90
Carl Zeiss 3d scanning
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Scanning, 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/3d scanning/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
3d scanning - by Bioz Stars, 2026-05
90/100 stars
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3d laser scanning microscope kj 3d  (KEYENCE)
90
KEYENCE 3d laser scanning microscope kj 3d
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Laser Scanning Microscope Kj 3d, supplied by KEYENCE, 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/3d laser scanning microscope kj 3d/product/KEYENCE
Average 90 stars, based on 1 article reviews
3d laser scanning microscope kj 3d - by Bioz Stars, 2026-05
90/100 stars
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3d computed tomography (ct) scans  (Siemens AG)
90
Siemens AG 3d computed tomography (ct) scans
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Computed Tomography (Ct) Scans, supplied by Siemens AG, 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/3d computed tomography (ct) scans/product/Siemens AG
Average 90 stars, based on 1 article reviews
3d computed tomography (ct) scans - by Bioz Stars, 2026-05
90/100 stars
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3d confocal raman microscope-spectrometer confotec duo  (SOL Instruments GmbH)
90
SOL Instruments GmbH 3d confocal raman microscope-spectrometer confotec duo
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Confocal Raman Microscope Spectrometer Confotec Duo, supplied by SOL Instruments GmbH, 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/3d confocal raman microscope-spectrometer confotec duo/product/SOL Instruments GmbH
Average 90 stars, based on 1 article reviews
3d confocal raman microscope-spectrometer confotec duo - by Bioz Stars, 2026-05
90/100 stars
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3d-scanned model  (COMSOL Inc)
90
COMSOL Inc 3d-scanned model
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Scanned Model, supplied by COMSOL 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/3d-scanned model/product/COMSOL Inc
Average 90 stars, based on 1 article reviews
3d-scanned model - by Bioz Stars, 2026-05
90/100 stars
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3d laser scanning equipment vke9700k  (KEYENCE)
90
KEYENCE 3d laser scanning equipment vke9700k
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Laser Scanning Equipment Vke9700k, supplied by KEYENCE, 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/3d laser scanning equipment vke9700k/product/KEYENCE
Average 90 stars, based on 1 article reviews
3d laser scanning equipment vke9700k - by Bioz Stars, 2026-05
90/100 stars
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cone beam computed tomography vatech pax-reve 3d plus  (VATECH Inc)
90
VATECH Inc cone beam computed tomography vatech pax-reve 3d plus
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
Cone Beam Computed Tomography Vatech Pax Reve 3d Plus, supplied by VATECH 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/cone beam computed tomography vatech pax-reve 3d plus/product/VATECH Inc
Average 90 stars, based on 1 article reviews
cone beam computed tomography vatech pax-reve 3d plus - by Bioz Stars, 2026-05
90/100 stars
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robotic fluoroscopy system artis zeego  (Siemens AG)
90
Siemens AG robotic fluoroscopy system artis zeego
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
Robotic Fluoroscopy System Artis Zeego, supplied by Siemens AG, 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/robotic fluoroscopy system artis zeego/product/Siemens AG
Average 90 stars, based on 1 article reviews
robotic fluoroscopy system artis zeego - by Bioz Stars, 2026-05
90/100 stars
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6x6 macular cube scan 3d oct  (topcon corporation)
90
topcon corporation 6x6 macular cube scan 3d oct
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
6x6 Macular Cube Scan 3d Oct, supplied by topcon corporation, 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/6x6 macular cube scan 3d oct/product/topcon corporation
Average 90 stars, based on 1 article reviews
6x6 macular cube scan 3d oct - by Bioz Stars, 2026-05
90/100 stars
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3d reconstruction of the ct scan terarecon aquarius intuiton  (TeraRecon)
90
TeraRecon 3d reconstruction of the ct scan terarecon aquarius intuiton
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Reconstruction Of The Ct Scan Terarecon Aquarius Intuiton, supplied by TeraRecon, 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/3d reconstruction of the ct scan terarecon aquarius intuiton/product/TeraRecon
Average 90 stars, based on 1 article reviews
3d reconstruction of the ct scan terarecon aquarius intuiton - by Bioz Stars, 2026-05
90/100 stars
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3d image scanning device  (PMDTechnologies ag)
90
PMDTechnologies ag 3d image scanning device
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Image Scanning Device, supplied by PMDTechnologies ag, 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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three-dimensional (3d) torso surface scans eva  (ARTEC CO LTD)
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A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
Three Dimensional (3d) Torso Surface Scans Eva, supplied by ARTEC CO 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/three-dimensional (3d) torso surface scans eva/product/ARTEC CO LTD
Average 90 stars, based on 1 article reviews
three-dimensional (3d) torso surface scans eva - by Bioz Stars, 2026-05
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Image Search Results


A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in 3D and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 in monolayer of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).

Journal: Nature Communications

Article Title: Scar matrix drives Piezo1 mediated stromal inflammation leading to placenta accreta spectrum

doi: 10.1038/s41467-024-52351-0

Figure Lengend Snippet: A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in 3D and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 in monolayer of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).

Article Snippet: After 4 days of decidualization, HTR8 spheroids prepared as aforementioned were suspended in 1 mg/ml collagen solution and plated on the 3D decidualization ESFs and incubated at 37 °C for 1 h to allow spheroid settle down and gel formation. dESF monolayer and HTR8 nuclear locations were recorded by Zeiss Apotome 3D scanning.

Techniques: Immunofluorescence, Enzyme-linked Immunosorbent Assay, Concentration Assay, Migration, Recombinant, Chemotaxis Assay, Labeling, Control, Two Tailed Test