3d surface rendering Search Results


static 3d surface-rendered ultrasound in obstetrics and gynecology 17  (Technik GmbH)
90
Technik GmbH static 3d surface-rendered ultrasound in obstetrics and gynecology 17
Static 3d Surface Rendered Ultrasound In Obstetrics And Gynecology 17, supplied by Technik 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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static 3d surface-rendered ultrasound in obstetrics and gynecology 17 - by Bioz Stars, 2026-08
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3d surface rendering (sr) of areas with increased 18 f-fdg uptake  (PMOD Technologies)
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PMOD Technologies 3d surface rendering (sr) of areas with increased 18 f-fdg uptake
3d Surface Rendering (Sr) Of Areas With Increased 18 F Fdg Uptake, supplied by PMOD Technologies, 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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3d surface rendering (sr) of areas with increased 18 f-fdg uptake - by Bioz Stars, 2026-08
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3d surface volume rendering of renal stones  (Dornheim Medical Images)
90
Dornheim Medical Images 3d surface volume rendering of renal stones
3d Surface Volume Rendering Of Renal Stones, supplied by Dornheim Medical Images, 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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3d surface volume rendering of renal stones - by Bioz Stars, 2026-08
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3d surface-rendered images  (SVI Huygens Software)
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SVI Huygens Software 3d surface-rendered images
Alpha-synuclein induces autophagy in microglial cells. (A) BV2 microglial cells were left untreated or stimulated at different time points with AS monomers (mAS) or fibrils (fAS) at 1 μM. Cells were then fixed and stained for LC3. (B–H) BV2 GFP–LC3 cells (B,C) or primary microglial cells (F,G) were left untreated or stimulated with Alexa Fluor 647-labelled AS fibrils (1 µM). After 12 h cells were immunostained with anti-LAMP1 (red) antibody and primary microglial cells were also stained for LC3. Images shown are z-stack projections. (D,H) 3D surface-rendered magnifications of the selected area above. (E,I) Mean±s.e.m. LC3-positive vesicles in unstimulated or treated BV2 (E) and primary microglial cells (I) were determined using ImageJ particle counting plugin after cell <t>deconvolution</t> (n=20). (J) Cell lysates from BV2 cells cultured with AS fibrils or monomers (1 µM) were collected at different time points and LC3 and β-actin protein levels were examined using western immunoblotting. Bafilomycin A1 (BAF) was added for the last 3 h. Graph shows quantification of mean±s.e.m. LC3-II expression relative to β-actin using densitometry. Results from at least three independent experiments were analysed by one-way ANOVA followed by post-hoc Dunnet's test; n=3. **P<0.01; ***P<0.001; #P<0.01 when comparing AS at 12 h (AS12) with AS at 12 h in the presence of BAF (AS12+BAF); Nd, no significant difference. pMC, primary microglial cells.
3d Surface Rendered Images, supplied by SVI Huygens Software, 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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3d surface-rendered images - by Bioz Stars, 2026-08
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surface-rendered models of 3d data sets of glomerular capillary casts  (Mercury Computer Systems Inc)
90
Mercury Computer Systems Inc surface-rendered models of 3d data sets of glomerular capillary casts
Alpha-synuclein induces autophagy in microglial cells. (A) BV2 microglial cells were left untreated or stimulated at different time points with AS monomers (mAS) or fibrils (fAS) at 1 μM. Cells were then fixed and stained for LC3. (B–H) BV2 GFP–LC3 cells (B,C) or primary microglial cells (F,G) were left untreated or stimulated with Alexa Fluor 647-labelled AS fibrils (1 µM). After 12 h cells were immunostained with anti-LAMP1 (red) antibody and primary microglial cells were also stained for LC3. Images shown are z-stack projections. (D,H) 3D surface-rendered magnifications of the selected area above. (E,I) Mean±s.e.m. LC3-positive vesicles in unstimulated or treated BV2 (E) and primary microglial cells (I) were determined using ImageJ particle counting plugin after cell <t>deconvolution</t> (n=20). (J) Cell lysates from BV2 cells cultured with AS fibrils or monomers (1 µM) were collected at different time points and LC3 and β-actin protein levels were examined using western immunoblotting. Bafilomycin A1 (BAF) was added for the last 3 h. Graph shows quantification of mean±s.e.m. LC3-II expression relative to β-actin using densitometry. Results from at least three independent experiments were analysed by one-way ANOVA followed by post-hoc Dunnet's test; n=3. **P<0.01; ***P<0.001; #P<0.01 when comparing AS at 12 h (AS12) with AS at 12 h in the presence of BAF (AS12+BAF); Nd, no significant difference. pMC, primary microglial cells.
Surface Rendered Models Of 3d Data Sets Of Glomerular Capillary Casts, supplied by Mercury Computer Systems 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+surface+rendering/10__1017_slash_s143192760606034x-34-7-17?v=Mercury+Computer+Systems+Inc
Average 90 stars, based on 1 article reviews
surface-rendered models of 3d data sets of glomerular capillary casts - by Bioz Stars, 2026-08
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surface rendering-3d-rekonstruktion  (Anwendung GmbH)
90
Anwendung GmbH surface rendering-3d-rekonstruktion
Alpha-synuclein induces autophagy in microglial cells. (A) BV2 microglial cells were left untreated or stimulated at different time points with AS monomers (mAS) or fibrils (fAS) at 1 μM. Cells were then fixed and stained for LC3. (B–H) BV2 GFP–LC3 cells (B,C) or primary microglial cells (F,G) were left untreated or stimulated with Alexa Fluor 647-labelled AS fibrils (1 µM). After 12 h cells were immunostained with anti-LAMP1 (red) antibody and primary microglial cells were also stained for LC3. Images shown are z-stack projections. (D,H) 3D surface-rendered magnifications of the selected area above. (E,I) Mean±s.e.m. LC3-positive vesicles in unstimulated or treated BV2 (E) and primary microglial cells (I) were determined using ImageJ particle counting plugin after cell <t>deconvolution</t> (n=20). (J) Cell lysates from BV2 cells cultured with AS fibrils or monomers (1 µM) were collected at different time points and LC3 and β-actin protein levels were examined using western immunoblotting. Bafilomycin A1 (BAF) was added for the last 3 h. Graph shows quantification of mean±s.e.m. LC3-II expression relative to β-actin using densitometry. Results from at least three independent experiments were analysed by one-way ANOVA followed by post-hoc Dunnet's test; n=3. **P<0.01; ***P<0.001; #P<0.01 when comparing AS at 12 h (AS12) with AS at 12 h in the presence of BAF (AS12+BAF); Nd, no significant difference. pMC, primary microglial cells.
Surface Rendering 3d Rekonstruktion, supplied by Anwendung 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+surface+rendering/pm11552384-76-0-2?v=Anwendung+GmbH
Average 90 stars, based on 1 article reviews
surface rendering-3d-rekonstruktion - by Bioz Stars, 2026-08
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Image Search Results


Alpha-synuclein induces autophagy in microglial cells. (A) BV2 microglial cells were left untreated or stimulated at different time points with AS monomers (mAS) or fibrils (fAS) at 1 μM. Cells were then fixed and stained for LC3. (B–H) BV2 GFP–LC3 cells (B,C) or primary microglial cells (F,G) were left untreated or stimulated with Alexa Fluor 647-labelled AS fibrils (1 µM). After 12 h cells were immunostained with anti-LAMP1 (red) antibody and primary microglial cells were also stained for LC3. Images shown are z-stack projections. (D,H) 3D surface-rendered magnifications of the selected area above. (E,I) Mean±s.e.m. LC3-positive vesicles in unstimulated or treated BV2 (E) and primary microglial cells (I) were determined using ImageJ particle counting plugin after cell deconvolution (n=20). (J) Cell lysates from BV2 cells cultured with AS fibrils or monomers (1 µM) were collected at different time points and LC3 and β-actin protein levels were examined using western immunoblotting. Bafilomycin A1 (BAF) was added for the last 3 h. Graph shows quantification of mean±s.e.m. LC3-II expression relative to β-actin using densitometry. Results from at least three independent experiments were analysed by one-way ANOVA followed by post-hoc Dunnet's test; n=3. **P<0.01; ***P<0.001; #P<0.01 when comparing AS at 12 h (AS12) with AS at 12 h in the presence of BAF (AS12+BAF); Nd, no significant difference. pMC, primary microglial cells.

Journal: Journal of Cell Science

Article Title: Alpha-synuclein fibrils recruit TBK1 and OPTN to lysosomal damage sites and induce autophagy in microglial cells

doi: 10.1242/jcs.226241

Figure Lengend Snippet: Alpha-synuclein induces autophagy in microglial cells. (A) BV2 microglial cells were left untreated or stimulated at different time points with AS monomers (mAS) or fibrils (fAS) at 1 μM. Cells were then fixed and stained for LC3. (B–H) BV2 GFP–LC3 cells (B,C) or primary microglial cells (F,G) were left untreated or stimulated with Alexa Fluor 647-labelled AS fibrils (1 µM). After 12 h cells were immunostained with anti-LAMP1 (red) antibody and primary microglial cells were also stained for LC3. Images shown are z-stack projections. (D,H) 3D surface-rendered magnifications of the selected area above. (E,I) Mean±s.e.m. LC3-positive vesicles in unstimulated or treated BV2 (E) and primary microglial cells (I) were determined using ImageJ particle counting plugin after cell deconvolution (n=20). (J) Cell lysates from BV2 cells cultured with AS fibrils or monomers (1 µM) were collected at different time points and LC3 and β-actin protein levels were examined using western immunoblotting. Bafilomycin A1 (BAF) was added for the last 3 h. Graph shows quantification of mean±s.e.m. LC3-II expression relative to β-actin using densitometry. Results from at least three independent experiments were analysed by one-way ANOVA followed by post-hoc Dunnet's test; n=3. **P<0.01; ***P<0.001; #P<0.01 when comparing AS at 12 h (AS12) with AS at 12 h in the presence of BAF (AS12+BAF); Nd, no significant difference. pMC, primary microglial cells.

Article Snippet: Spatial deconvolution, 3D surface-rendered images and 3D surface-rendered movies were created with SVI Huygens Software.

Techniques: Staining, Cell Culture, Western Blot, Expressing