3d surface rendering Search Results


static 3d surface-rendered ultrasound in obstetrics and gynecology 17  (Technik GmbH)
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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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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 volume rendering of renal stones  (Dornheim Medical Images)
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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-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, 2026-09
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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
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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/surface+rendering+3d+rekonstruktion/pm11552384-76-0-2
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surface rendering-3d-rekonstruktion - by Bioz Stars, 2026-09
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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