3d applications Search Results


102-3d  (cell applications inc)
93
cell applications inc 102-3d
102 3d, supplied by cell applications inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/3d+applications/pmc06615970-18-0-4?v=cell+applications+inc
Average 93 stars, based on 1 article reviews
102-3d - by Bioz Stars, 2026-07
93/100 stars
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sodium fluoride  (Chem Impex International)
95
Chem Impex International sodium fluoride
Sodium Fluoride, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/3d+applications/bio_rxiv__2022__01__04__474939-144-85-87?v=Chem+Impex+International
Average 95 stars, based on 1 article reviews
sodium fluoride - by Bioz Stars, 2026-07
95/100 stars
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airway model  (Cell Applications Inc)
91
Cell Applications Inc airway model
Airway Model, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/3d+applications/pmc10615614-307-2-5?v=Cell+Applications+Inc
Average 91 stars, based on 1 article reviews
airway model - by Bioz Stars, 2026-07
91/100 stars
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primary hnscs  (Cell Applications Inc)
93
Cell Applications Inc primary hnscs
STEE and its major polyphenolic constituents stimulated the mitochondrial activity of <t>hNSCs-derived</t> immature astrocytes. ( A ) hNSCs were plated in a 96 well plate, induced differentiation into astrocytes, and pre-treated with STEE and its major constituents; 3CQA, 5CQA, 3FQA, or ISO, for the indicated times (24, 48, or 72 h). Cells were then further incubated with Rh123 for 20 min, and the fluorescence intensity generated by Rh123 was monitored at λex = 507 nm and λem = 529 nm. The percentages shown are the mean ± SEM (n = 3–6). One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05. ( B ) Cells were incubated with STEE and its constituents for 48 h, and PGC-1α mRNA ( PPARGC1 ) expression was measured. The relative values are the mean ± SEM (n = 3) compared with the control. One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05, **** p < 0.0001. A description of the number for the treatment groups is indicated in . ( C ) Phase-contrast microphotographs of hNSC-derived <t>astrocytes</t> <t>cultured</t> for 48 h in the absence or presence of STEE (50 µg/mL). High magnification views of boxed areas are shown below panels. Scale bar = 50 µm in panels and 20 μm in insets.
Primary Hnscs, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/3d+applications/pmc09738893-170-0-3?v=Cell+Applications+Inc
Average 93 stars, based on 1 article reviews
primary hnscs - by Bioz Stars, 2026-07
93/100 stars
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smartphone free application bellus 3d  (Bellus Health)
90
Bellus Health smartphone free application bellus 3d
STEE and its major polyphenolic constituents stimulated the mitochondrial activity of <t>hNSCs-derived</t> immature astrocytes. ( A ) hNSCs were plated in a 96 well plate, induced differentiation into astrocytes, and pre-treated with STEE and its major constituents; 3CQA, 5CQA, 3FQA, or ISO, for the indicated times (24, 48, or 72 h). Cells were then further incubated with Rh123 for 20 min, and the fluorescence intensity generated by Rh123 was monitored at λex = 507 nm and λem = 529 nm. The percentages shown are the mean ± SEM (n = 3–6). One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05. ( B ) Cells were incubated with STEE and its constituents for 48 h, and PGC-1α mRNA ( PPARGC1 ) expression was measured. The relative values are the mean ± SEM (n = 3) compared with the control. One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05, **** p < 0.0001. A description of the number for the treatment groups is indicated in . ( C ) Phase-contrast microphotographs of hNSC-derived <t>astrocytes</t> <t>cultured</t> for 48 h in the absence or presence of STEE (50 µg/mL). High magnification views of boxed areas are shown below panels. Scale bar = 50 µm in panels and 20 μm in insets.
Smartphone Free Application Bellus 3d, supplied by Bellus Health, 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/product/3d+applications/pm33571145-51-20-23?v=Bellus+Health
Average 90 stars, based on 1 article reviews
smartphone free application bellus 3d - by Bioz Stars, 2026-07
90/100 stars
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3d laser scanner nextec hawk  (Nextec Applications Inc)
90
Nextec Applications Inc 3d laser scanner nextec hawk
STEE and its major polyphenolic constituents stimulated the mitochondrial activity of <t>hNSCs-derived</t> immature astrocytes. ( A ) hNSCs were plated in a 96 well plate, induced differentiation into astrocytes, and pre-treated with STEE and its major constituents; 3CQA, 5CQA, 3FQA, or ISO, for the indicated times (24, 48, or 72 h). Cells were then further incubated with Rh123 for 20 min, and the fluorescence intensity generated by Rh123 was monitored at λex = 507 nm and λem = 529 nm. The percentages shown are the mean ± SEM (n = 3–6). One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05. ( B ) Cells were incubated with STEE and its constituents for 48 h, and PGC-1α mRNA ( PPARGC1 ) expression was measured. The relative values are the mean ± SEM (n = 3) compared with the control. One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05, **** p < 0.0001. A description of the number for the treatment groups is indicated in . ( C ) Phase-contrast microphotographs of hNSC-derived <t>astrocytes</t> <t>cultured</t> for 48 h in the absence or presence of STEE (50 µg/mL). High magnification views of boxed areas are shown below panels. Scale bar = 50 µm in panels and 20 μm in insets.
3d Laser Scanner Nextec Hawk, supplied by Nextec Applications 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/product/3d+applications/pmc04212904__pone__0109528__s001-2-2-8?v=Nextec+Applications+Inc
Average 90 stars, based on 1 article reviews
3d laser scanner nextec hawk - by Bioz Stars, 2026-07
90/100 stars
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3d laser microfabrication  (Verlag GmbH)
90
Verlag GmbH 3d laser microfabrication
STEE and its major polyphenolic constituents stimulated the mitochondrial activity of <t>hNSCs-derived</t> immature astrocytes. ( A ) hNSCs were plated in a 96 well plate, induced differentiation into astrocytes, and pre-treated with STEE and its major constituents; 3CQA, 5CQA, 3FQA, or ISO, for the indicated times (24, 48, or 72 h). Cells were then further incubated with Rh123 for 20 min, and the fluorescence intensity generated by Rh123 was monitored at λex = 507 nm and λem = 529 nm. The percentages shown are the mean ± SEM (n = 3–6). One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05. ( B ) Cells were incubated with STEE and its constituents for 48 h, and PGC-1α mRNA ( PPARGC1 ) expression was measured. The relative values are the mean ± SEM (n = 3) compared with the control. One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05, **** p < 0.0001. A description of the number for the treatment groups is indicated in . ( C ) Phase-contrast microphotographs of hNSC-derived <t>astrocytes</t> <t>cultured</t> for 48 h in the absence or presence of STEE (50 µg/mL). High magnification views of boxed areas are shown below panels. Scale bar = 50 µm in panels and 20 μm in insets.
3d Laser Microfabrication, 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
https://www.bioz.com/product/3d+applications/10__1016_slash_j__apsusc__2011__12__020-128-4-10?v=Verlag+GmbH
Average 90 stars, based on 1 article reviews
3d laser microfabrication - by Bioz Stars, 2026-07
90/100 stars
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3d medsim application  (Medsim Inc)
90
Medsim Inc 3d medsim application
STEE and its major polyphenolic constituents stimulated the mitochondrial activity of <t>hNSCs-derived</t> immature astrocytes. ( A ) hNSCs were plated in a 96 well plate, induced differentiation into astrocytes, and pre-treated with STEE and its major constituents; 3CQA, 5CQA, 3FQA, or ISO, for the indicated times (24, 48, or 72 h). Cells were then further incubated with Rh123 for 20 min, and the fluorescence intensity generated by Rh123 was monitored at λex = 507 nm and λem = 529 nm. The percentages shown are the mean ± SEM (n = 3–6). One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05. ( B ) Cells were incubated with STEE and its constituents for 48 h, and PGC-1α mRNA ( PPARGC1 ) expression was measured. The relative values are the mean ± SEM (n = 3) compared with the control. One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05, **** p < 0.0001. A description of the number for the treatment groups is indicated in . ( C ) Phase-contrast microphotographs of hNSC-derived <t>astrocytes</t> <t>cultured</t> for 48 h in the absence or presence of STEE (50 µg/mL). High magnification views of boxed areas are shown below panels. Scale bar = 50 µm in panels and 20 μm in insets.
3d Medsim Application, supplied by Medsim 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/product/3d+applications/pm40619367-103-15-16?v=Medsim+Inc
Average 90 stars, based on 1 article reviews
3d medsim application - by Bioz Stars, 2026-07
90/100 stars
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applications from bellus 3d  (Bellus Health)
90
Bellus Health applications from bellus 3d
STEE and its major polyphenolic constituents stimulated the mitochondrial activity of <t>hNSCs-derived</t> immature astrocytes. ( A ) hNSCs were plated in a 96 well plate, induced differentiation into astrocytes, and pre-treated with STEE and its major constituents; 3CQA, 5CQA, 3FQA, or ISO, for the indicated times (24, 48, or 72 h). Cells were then further incubated with Rh123 for 20 min, and the fluorescence intensity generated by Rh123 was monitored at λex = 507 nm and λem = 529 nm. The percentages shown are the mean ± SEM (n = 3–6). One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05. ( B ) Cells were incubated with STEE and its constituents for 48 h, and PGC-1α mRNA ( PPARGC1 ) expression was measured. The relative values are the mean ± SEM (n = 3) compared with the control. One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05, **** p < 0.0001. A description of the number for the treatment groups is indicated in . ( C ) Phase-contrast microphotographs of hNSC-derived <t>astrocytes</t> <t>cultured</t> for 48 h in the absence or presence of STEE (50 µg/mL). High magnification views of boxed areas are shown below panels. Scale bar = 50 µm in panels and 20 μm in insets.
Applications From Bellus 3d, supplied by Bellus Health, 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/product/3d+applications/pmc11654360-236-41-2?v=Bellus+Health
Average 90 stars, based on 1 article reviews
applications from bellus 3d - by Bioz Stars, 2026-07
90/100 stars
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ct pulmo 3d application  (Siemens AG)
90
Siemens AG ct pulmo 3d application
STEE and its major polyphenolic constituents stimulated the mitochondrial activity of <t>hNSCs-derived</t> immature astrocytes. ( A ) hNSCs were plated in a 96 well plate, induced differentiation into astrocytes, and pre-treated with STEE and its major constituents; 3CQA, 5CQA, 3FQA, or ISO, for the indicated times (24, 48, or 72 h). Cells were then further incubated with Rh123 for 20 min, and the fluorescence intensity generated by Rh123 was monitored at λex = 507 nm and λem = 529 nm. The percentages shown are the mean ± SEM (n = 3–6). One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05. ( B ) Cells were incubated with STEE and its constituents for 48 h, and PGC-1α mRNA ( PPARGC1 ) expression was measured. The relative values are the mean ± SEM (n = 3) compared with the control. One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05, **** p < 0.0001. A description of the number for the treatment groups is indicated in . ( C ) Phase-contrast microphotographs of hNSC-derived <t>astrocytes</t> <t>cultured</t> for 48 h in the absence or presence of STEE (50 µg/mL). High magnification views of boxed areas are shown below panels. Scale bar = 50 µm in panels and 20 μm in insets.
Ct Pulmo 3d Application, 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/product/3d+applications/pmc11265689-62-7-17?v=Siemens+AG
Average 90 stars, based on 1 article reviews
ct pulmo 3d application - by Bioz Stars, 2026-07
90/100 stars
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syngo.via database comparison  (Siemens AG)
90
Siemens AG syngo.via database comparison
STEE and its major polyphenolic constituents stimulated the mitochondrial activity of <t>hNSCs-derived</t> immature astrocytes. ( A ) hNSCs were plated in a 96 well plate, induced differentiation into astrocytes, and pre-treated with STEE and its major constituents; 3CQA, 5CQA, 3FQA, or ISO, for the indicated times (24, 48, or 72 h). Cells were then further incubated with Rh123 for 20 min, and the fluorescence intensity generated by Rh123 was monitored at λex = 507 nm and λem = 529 nm. The percentages shown are the mean ± SEM (n = 3–6). One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05. ( B ) Cells were incubated with STEE and its constituents for 48 h, and PGC-1α mRNA ( PPARGC1 ) expression was measured. The relative values are the mean ± SEM (n = 3) compared with the control. One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05, **** p < 0.0001. A description of the number for the treatment groups is indicated in . ( C ) Phase-contrast microphotographs of hNSC-derived <t>astrocytes</t> <t>cultured</t> for 48 h in the absence or presence of STEE (50 µg/mL). High magnification views of boxed areas are shown below panels. Scale bar = 50 µm in panels and 20 μm in insets.
Syngo.Via Database Comparison, 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/product/3d+applications/pmc07344773-17-12-14?v=Siemens+AG
Average 90 stars, based on 1 article reviews
syngo.via database comparison - by Bioz Stars, 2026-07
90/100 stars
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3d cad principles and applications  (Verlag GmbH)
90
Verlag GmbH 3d cad principles and applications
STEE and its major polyphenolic constituents stimulated the mitochondrial activity of <t>hNSCs-derived</t> immature astrocytes. ( A ) hNSCs were plated in a 96 well plate, induced differentiation into astrocytes, and pre-treated with STEE and its major constituents; 3CQA, 5CQA, 3FQA, or ISO, for the indicated times (24, 48, or 72 h). Cells were then further incubated with Rh123 for 20 min, and the fluorescence intensity generated by Rh123 was monitored at λex = 507 nm and λem = 529 nm. The percentages shown are the mean ± SEM (n = 3–6). One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05. ( B ) Cells were incubated with STEE and its constituents for 48 h, and PGC-1α mRNA ( PPARGC1 ) expression was measured. The relative values are the mean ± SEM (n = 3) compared with the control. One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05, **** p < 0.0001. A description of the number for the treatment groups is indicated in . ( C ) Phase-contrast microphotographs of hNSC-derived <t>astrocytes</t> <t>cultured</t> for 48 h in the absence or presence of STEE (50 µg/mL). High magnification views of boxed areas are shown below panels. Scale bar = 50 µm in panels and 20 μm in insets.
3d Cad Principles And Applications, 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
https://www.bioz.com/product/3d+applications/us07372558-150-0-5?v=Verlag+GmbH
Average 90 stars, based on 1 article reviews
3d cad principles and applications - by Bioz Stars, 2026-07
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Image Search Results


STEE and its major polyphenolic constituents stimulated the mitochondrial activity of hNSCs-derived immature astrocytes. ( A ) hNSCs were plated in a 96 well plate, induced differentiation into astrocytes, and pre-treated with STEE and its major constituents; 3CQA, 5CQA, 3FQA, or ISO, for the indicated times (24, 48, or 72 h). Cells were then further incubated with Rh123 for 20 min, and the fluorescence intensity generated by Rh123 was monitored at λex = 507 nm and λem = 529 nm. The percentages shown are the mean ± SEM (n = 3–6). One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05. ( B ) Cells were incubated with STEE and its constituents for 48 h, and PGC-1α mRNA ( PPARGC1 ) expression was measured. The relative values are the mean ± SEM (n = 3) compared with the control. One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05, **** p < 0.0001. A description of the number for the treatment groups is indicated in . ( C ) Phase-contrast microphotographs of hNSC-derived astrocytes cultured for 48 h in the absence or presence of STEE (50 µg/mL). High magnification views of boxed areas are shown below panels. Scale bar = 50 µm in panels and 20 μm in insets.

Journal: International Journal of Molecular Sciences

Article Title: Interactions between Major Bioactive Polyphenols of Sugarcane Top: Effects on Human Neural Stem Cell Differentiation and Astrocytic Maturation

doi: 10.3390/ijms232315120

Figure Lengend Snippet: STEE and its major polyphenolic constituents stimulated the mitochondrial activity of hNSCs-derived immature astrocytes. ( A ) hNSCs were plated in a 96 well plate, induced differentiation into astrocytes, and pre-treated with STEE and its major constituents; 3CQA, 5CQA, 3FQA, or ISO, for the indicated times (24, 48, or 72 h). Cells were then further incubated with Rh123 for 20 min, and the fluorescence intensity generated by Rh123 was monitored at λex = 507 nm and λem = 529 nm. The percentages shown are the mean ± SEM (n = 3–6). One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05. ( B ) Cells were incubated with STEE and its constituents for 48 h, and PGC-1α mRNA ( PPARGC1 ) expression was measured. The relative values are the mean ± SEM (n = 3) compared with the control. One-way ANOVA with Dunnett’s post hoc test for the comparisons: * p < 0.05, **** p < 0.0001. A description of the number for the treatment groups is indicated in . ( C ) Phase-contrast microphotographs of hNSC-derived astrocytes cultured for 48 h in the absence or presence of STEE (50 µg/mL). High magnification views of boxed areas are shown below panels. Scale bar = 50 µm in panels and 20 μm in insets.

Article Snippet: Primary hNSCs (HS820-20f, Cell Applications, San Diego, CA, USA) were cultured as previously reported [ ].

Techniques: Activity Assay, Derivative Assay, Incubation, Fluorescence, Generated, Expressing, Control, Cell Culture