eb3 Search Results


fip1  (Addgene inc)
90
Addgene inc fip1
Fip1, supplied by Addgene 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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eb3 mneongreen chertkova  (Addgene inc)
93
Addgene inc eb3 mneongreen chertkova
Eb3 Mneongreen Chertkova, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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eb3 tdtomato  (Addgene inc)
93
Addgene inc eb3 tdtomato
Eb3 Tdtomato, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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eb3  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology eb3
Figure 1. The centrosome is not essential for angiogenic migration and sprouting. (A) Imaging of control or centrinone-treated HUVECs stained for MT (a-tubulin, cyan hot) using STED microscopy. Arrow points toward the centrosome and the plot shows the average fluorescence intensity of a-tubulin, n = 25 cells for each condition. (B,C) Analysis of MT plus ends in control or centrinone-treated HUVECs illustrated by maximum intensity projections and kymographs of <t>EB3-GFP</t> live fluorescence imaging (B) and <t>EB3</t> staining (C). Plots show MT growth rate and catastrophe frequency, n = 96 tracks in Figure 1 continued on next page
Eb3, supplied by Santa Cruz Biotechnology, 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/result/eb3/product/Santa Cruz Biotechnology
Average 93 stars, based on 1 article reviews
eb3 - by Bioz Stars, 2026-04
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memerald eb3 c 20 plasmid  (Addgene inc)
92
Addgene inc memerald eb3 c 20 plasmid
Figure 1. The centrosome is not essential for angiogenic migration and sprouting. (A) Imaging of control or centrinone-treated HUVECs stained for MT (a-tubulin, cyan hot) using STED microscopy. Arrow points toward the centrosome and the plot shows the average fluorescence intensity of a-tubulin, n = 25 cells for each condition. (B,C) Analysis of MT plus ends in control or centrinone-treated HUVECs illustrated by maximum intensity projections and kymographs of <t>EB3-GFP</t> live fluorescence imaging (B) and <t>EB3</t> staining (C). Plots show MT growth rate and catastrophe frequency, n = 96 tracks in Figure 1 continued on next page
Memerald Eb3 C 20 Plasmid, supplied by Addgene inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pegfp centrin2 vectors  (Addgene inc)
88
Addgene inc pegfp centrin2 vectors
Figure 1. The centrosome is not essential for angiogenic migration and sprouting. (A) Imaging of control or centrinone-treated HUVECs stained for MT (a-tubulin, cyan hot) using STED microscopy. Arrow points toward the centrosome and the plot shows the average fluorescence intensity of a-tubulin, n = 25 cells for each condition. (B,C) Analysis of MT plus ends in control or centrinone-treated HUVECs illustrated by maximum intensity projections and kymographs of <t>EB3-GFP</t> live fluorescence imaging (B) and <t>EB3</t> staining (C). Plots show MT growth rate and catastrophe frequency, n = 96 tracks in Figure 1 continued on next page
Pegfp Centrin2 Vectors, supplied by Addgene inc, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pegfp centrin2 vectors - by Bioz Stars, 2026-04
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addgene plasmid  (Addgene inc)
90
Addgene inc addgene plasmid
Figure 1. The centrosome is not essential for angiogenic migration and sprouting. (A) Imaging of control or centrinone-treated HUVECs stained for MT (a-tubulin, cyan hot) using STED microscopy. Arrow points toward the centrosome and the plot shows the average fluorescence intensity of a-tubulin, n = 25 cells for each condition. (B,C) Analysis of MT plus ends in control or centrinone-treated HUVECs illustrated by maximum intensity projections and kymographs of <t>EB3-GFP</t> live fluorescence imaging (B) and <t>EB3</t> staining (C). Plots show MT growth rate and catastrophe frequency, n = 96 tracks in Figure 1 continued on next page
Addgene Plasmid, supplied by Addgene 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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mscarlet  (Addgene inc)
93
Addgene inc mscarlet
Figure 1. The centrosome is not essential for angiogenic migration and sprouting. (A) Imaging of control or centrinone-treated HUVECs stained for MT (a-tubulin, cyan hot) using STED microscopy. Arrow points toward the centrosome and the plot shows the average fluorescence intensity of a-tubulin, n = 25 cells for each condition. (B,C) Analysis of MT plus ends in control or centrinone-treated HUVECs illustrated by maximum intensity projections and kymographs of <t>EB3-GFP</t> live fluorescence imaging (B) and <t>EB3</t> staining (C). Plots show MT growth rate and catastrophe frequency, n = 96 tracks in Figure 1 continued on next page
Mscarlet, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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michael davidson plasmid collection  (Addgene inc)
93
Addgene inc michael davidson plasmid collection
Figure 1. The centrosome is not essential for angiogenic migration and sprouting. (A) Imaging of control or centrinone-treated HUVECs stained for MT (a-tubulin, cyan hot) using STED microscopy. Arrow points toward the centrosome and the plot shows the average fluorescence intensity of a-tubulin, n = 25 cells for each condition. (B,C) Analysis of MT plus ends in control or centrinone-treated HUVECs illustrated by maximum intensity projections and kymographs of <t>EB3-GFP</t> live fluorescence imaging (B) and <t>EB3</t> staining (C). Plots show MT growth rate and catastrophe frequency, n = 96 tracks in Figure 1 continued on next page
Michael Davidson Plasmid Collection, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fugene 6  (Addgene inc)
93
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Figure 1. The centrosome is not essential for angiogenic migration and sprouting. (A) Imaging of control or centrinone-treated HUVECs stained for MT (a-tubulin, cyan hot) using STED microscopy. Arrow points toward the centrosome and the plot shows the average fluorescence intensity of a-tubulin, n = 25 cells for each condition. (B,C) Analysis of MT plus ends in control or centrinone-treated HUVECs illustrated by maximum intensity projections and kymographs of <t>EB3-GFP</t> live fluorescence imaging (B) and <t>EB3</t> staining (C). Plots show MT growth rate and catastrophe frequency, n = 96 tracks in Figure 1 continued on next page
Fugene 6, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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michael davidson  (Addgene inc)
91
Addgene inc michael davidson
Figure 1. The centrosome is not essential for angiogenic migration and sprouting. (A) Imaging of control or centrinone-treated HUVECs stained for MT (a-tubulin, cyan hot) using STED microscopy. Arrow points toward the centrosome and the plot shows the average fluorescence intensity of a-tubulin, n = 25 cells for each condition. (B,C) Analysis of MT plus ends in control or centrinone-treated HUVECs illustrated by maximum intensity projections and kymographs of <t>EB3-GFP</t> live fluorescence imaging (B) and <t>EB3</t> staining (C). Plots show MT growth rate and catastrophe frequency, n = 96 tracks in Figure 1 continued on next page
Michael Davidson, supplied by Addgene inc, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Figure 1. The centrosome is not essential for angiogenic migration and sprouting. (A) Imaging of control or centrinone-treated HUVECs stained for MT (a-tubulin, cyan hot) using STED microscopy. Arrow points toward the centrosome and the plot shows the average fluorescence intensity of a-tubulin, n = 25 cells for each condition. (B,C) Analysis of MT plus ends in control or centrinone-treated HUVECs illustrated by maximum intensity projections and kymographs of EB3-GFP live fluorescence imaging (B) and EB3 staining (C). Plots show MT growth rate and catastrophe frequency, n = 96 tracks in Figure 1 continued on next page

Journal: eLife

Article Title: Control of endothelial cell polarity and sprouting angiogenesis by non-centrosomal microtubules

doi: 10.7554/elife.33864

Figure Lengend Snippet: Figure 1. The centrosome is not essential for angiogenic migration and sprouting. (A) Imaging of control or centrinone-treated HUVECs stained for MT (a-tubulin, cyan hot) using STED microscopy. Arrow points toward the centrosome and the plot shows the average fluorescence intensity of a-tubulin, n = 25 cells for each condition. (B,C) Analysis of MT plus ends in control or centrinone-treated HUVECs illustrated by maximum intensity projections and kymographs of EB3-GFP live fluorescence imaging (B) and EB3 staining (C). Plots show MT growth rate and catastrophe frequency, n = 96 tracks in Figure 1 continued on next page

Article Snippet: We used rabbit polyclonal antibodies against CAMSAP2 (Novus, Littleton, CO, NBP1-21402), CEP135, acetylated tubulin, polyglutamylated tubulin and g-tubulin (Sigma-Aldrich, St Louis, MO, SAB4503685, T7451, T9822 and T3559), CDK5RAP2 (BethylLaboratories, Montgomery, TX, A300-554A), detyrosinated tubulin (Abcam, UK, ab48389), EB3 (Stepanova et al., 2003) and myomegalin isoform 8 (MMG8) (Wang et al., 2014), goat polyclonal antibodies against MYOSIN IIb and PCM1 (Santa-Cruz biotechnology, Dallas, TX, SC-47205 and SC-50164), mouse monoclonal anti- bodies against GM130, Pericentrin, EB1, VE-Cadherin, ZO-1, AKAP450 and KU80 (BD Biosciences, San Jose, CA, 610823, 611815, 610535, 610252, 610966, 611518 and 611360), CAMSAP3, a-tubulin and g-tubulin (Sigma-Aldrich, SAB4200415, T5168 and T6557), NEDD1 (Abnova, Taiwan, H00121441-M05) and rat monoclonal antibodies against a-tubulin YL1/2 (Pierce, Waltham, MA, MA1-80017).

Techniques: Migration, Imaging, Control, Staining, Microscopy, Fluorescence