tuj1 primary antibody Search Results


90
Becton Dickinson β-tubulin
β Tubulin, supplied by Becton Dickinson, 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/tuj1+primary+antibody/%CE%B2+tubulin+antibody/pm28656206-59-4-7
Average 90 stars, based on 1 article reviews
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Biozol Diagnostica Vertrieb GmbH tuj1 biozol 801202 antibody
Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and <t>TUJ1</t> + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.
Tuj1 Biozol 801202 Antibody, supplied by Biozol Diagnostica Vertrieb 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/tuj1+primary+antibody/tuj1+antibody/pmc06821804-209-3-4
Average 90 stars, based on 1 article reviews
tuj1 biozol 801202 antibody - by Bioz Stars, 2026-09
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90
MBL International rabbit anti-α-tubulin
Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and <t>TUJ1</t> + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.
Rabbit Anti α Tubulin, supplied by MBL International, 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/tuj1+primary+antibody/anti+%CE%B1+tubulin+antibody/pmc10075103-138-6-9
Average 90 stars, based on 1 article reviews
rabbit anti-α-tubulin - by Bioz Stars, 2026-09
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96
Proteintech tubulin
Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and <t>TUJ1</t> + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.
Tubulin, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/tuj1+primary+antibody/gamma+tubulin+Antibody/pmc12019514-94-9-18
Average 96 stars, based on 1 article reviews
tubulin - by Bioz Stars, 2026-09
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90
GeneTex neuronal class iii β-tubulin tuj-1 antibody
Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and <t>TUJ1</t> + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.
Neuronal Class Iii β Tubulin Tuj 1 Antibody, supplied by GeneTex, 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/tuj1+primary+antibody/tuj1+antibody/pmc11197294-147-5-10
Average 90 stars, based on 1 article reviews
neuronal class iii β-tubulin tuj-1 antibody - by Bioz Stars, 2026-09
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90
Promega mouse anti-βiii tubulin
Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and <t>TUJ1</t> + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.
Mouse Anti βiii Tubulin, supplied by Promega, 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/tuj1+primary+antibody/mouse+anti+%CE%B2iii+tubulin/pm20580711-88-6-10
Average 90 stars, based on 1 article reviews
mouse anti-βiii tubulin - by Bioz Stars, 2026-09
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90
Promega antimouse βiii-tubulin
Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and <t>TUJ1</t> + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.
Antimouse βiii Tubulin, supplied by Promega, 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/tuj1+primary+antibody/anti+%CE%B2iii+tubulin/10__22203_slash_ecm__v041a28-128-46-54
Average 90 stars, based on 1 article reviews
antimouse βiii-tubulin - by Bioz Stars, 2026-09
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96
R&D Systems mouse monoclonal anti β tubulin iii antibody
Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and <t>TUJ1</t> + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.
Mouse Monoclonal Anti β Tubulin Iii Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/tuj1+primary+antibody/Neuron-specific+beta-III+Tubulin+Antibody/pmc05948884-52-4-11
Average 96 stars, based on 1 article reviews
mouse monoclonal anti β tubulin iii antibody - by Bioz Stars, 2026-09
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86
Covance iii tubulin
Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and <t>TUJ1</t> + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.
Iii Tubulin, supplied by Covance, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/tuj1+primary+antibody/anti+tuj1/pm16787946-260-12-17
Average 86 stars, based on 1 article reviews
iii tubulin - by Bioz Stars, 2026-09
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97
Cell Signaling Technology Inc rabbit antibodies against β tubulin
Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and <t>TUJ1</t> + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.
Rabbit Antibodies Against β Tubulin, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/tuj1+primary+antibody/beta-Tubulin+Antibody/pmc09200745-121-6-11
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rabbit antibodies against β tubulin - by Bioz Stars, 2026-09
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96
Cell Signaling Technology Inc rabbit anti tubb3
Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and <t>TUJ1</t> + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.
Rabbit Anti Tubb3, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/tuj1+primary+antibody/beta3-Tubulin+XP+Rabbit+mAb/pmc10859526-86-4-13
Average 96 stars, based on 1 article reviews
rabbit anti tubb3 - by Bioz Stars, 2026-09
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97
Cell Signaling Technology Inc anti α tubulin
Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and <t>TUJ1</t> + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.
Anti α Tubulin, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/tuj1+primary+antibody/alpha-Tubulin+Antibody/pm37174666-72-3-5
Average 97 stars, based on 1 article reviews
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Image Search Results


Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and TUJ1 + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.

Journal: Scientific Reports

Article Title: Generation of complex human organoid models including vascular networks by incorporation of mesodermal progenitor cells

doi: 10.1038/s41598-019-52204-7

Figure Lengend Snippet: Characterization of vascularized neural organoids. Neural spheres consisting of Sox1 + neuroepithelial cells ( A ) and Brachyury + mesodermal spheres. ( B ) Spheres were brought in co-culture. The formation of chimeric neuro-mesodermal aggregates was observed ( C ). The aggregates were cultured for up to 280 days ( D ). ( E ) HE-staining of sections showing the interface between neuroepithelial (left side) and mesenchymal part (right side). ( F – G ) Immunofluorescence analyses showing the Pax6 + neuroepithelium and CD31 + endothelial cells. ( H – D ) The neural part consists of Sox1 + stem cells and TUJ1 + neurons. ( J – K ) At the interface between neuroepithelium and mesenchyme, CD31 + vessels form a perineural plexus. ( L ) A capillary at the perineural plexus in an ED 5 chicken embryo is depicted. Blood cells show green autofluorescence. ( M ) Within the mesodermal part an extensive network of blood vessels can be observed. M shows a maximum intensity projection of a whole mount stained organoid. ( N ) HE staining of paraffin sections from the mesodermal part of an organoid. The picture shows a vessel structure with clear lumen (asterisk) and a small capillary (arrowhead). ( O – S ) Transmission electron microscopic pictures showing the endothelium of vessel structures within the organoids. *Periendothelial cells, EC: endothelial cells, BM: basement membrane, IJ: intercellular junction, CV: caveolae, MV: microvesicle.

Article Snippet: Primary antibodies to TUJ1 (Biozol, 801202), GFAP (DAKO, Z0334), CD31 (DAKO, M0823), Iba1 (WAKO, 019-19741), Sox1 (R&D Systems, AF3369), Pax6 (Biolegend, 901301), Brachyury (T) (R&D Systems, AF2085), MAP2 (Abcam, AB32454), N-Cadherin (Sigma-Aldrich, C3865) and NG2 (Merck-Millipore, AB5320) were used.

Techniques: Co-Culture Assay, Cell Culture, Staining, Immunofluorescence, Transmission Assay, Membrane

Characterization of the neural part of the organoid. Pictures show organoids at culture day 210. ( A ) HE-stained sections reveal ventricle-like cavities inside the neural tissue. ( B – C ) Neuroepithelial cells lining the ventricle-like structures stain positive for Sox1 and Nestin, while the cells surrounding the stem cell zone express the neuronal marker protein MAP2. ( C ) Shows a higher magnification of B. ( D ) The apical side of the neuroepithelium is marked by N-Cadherin + cell-cell junctions. TUJ1 + cells can be found towards the basal side indicating neuronal differentiation. ( E ) Besides TUJ1 + neurons, GFAP + radial glia cells or astrocytes can be found located towards the basal side of the epithelium.

Journal: Scientific Reports

Article Title: Generation of complex human organoid models including vascular networks by incorporation of mesodermal progenitor cells

doi: 10.1038/s41598-019-52204-7

Figure Lengend Snippet: Characterization of the neural part of the organoid. Pictures show organoids at culture day 210. ( A ) HE-stained sections reveal ventricle-like cavities inside the neural tissue. ( B – C ) Neuroepithelial cells lining the ventricle-like structures stain positive for Sox1 and Nestin, while the cells surrounding the stem cell zone express the neuronal marker protein MAP2. ( C ) Shows a higher magnification of B. ( D ) The apical side of the neuroepithelium is marked by N-Cadherin + cell-cell junctions. TUJ1 + cells can be found towards the basal side indicating neuronal differentiation. ( E ) Besides TUJ1 + neurons, GFAP + radial glia cells or astrocytes can be found located towards the basal side of the epithelium.

Article Snippet: Primary antibodies to TUJ1 (Biozol, 801202), GFAP (DAKO, Z0334), CD31 (DAKO, M0823), Iba1 (WAKO, 019-19741), Sox1 (R&D Systems, AF3369), Pax6 (Biolegend, 901301), Brachyury (T) (R&D Systems, AF2085), MAP2 (Abcam, AB32454), N-Cadherin (Sigma-Aldrich, C3865) and NG2 (Merck-Millipore, AB5320) were used.

Techniques: Staining, Marker

Vascularization of the neural part of the organoid and invasion of microglia-like cells. ( A ) At day 180 a CD31 + endothelial network infiltrating the Pax6 + neural part of the organoid was observed. ( B ) shows a higher magnification of A. ( C ) Infiltrating vessels were found within the neural tissue surrounding Sox1 + neuroepithelial structures. ( D – E ) CD31 + capillaries within the neural part of the organoid closely associated with GFAP + astrocytes/radial glia and TUJ1 + neurons. ( F ) GFAP + cells form close contacts with CD31 + endothelial cells (see inset). ( G ) Iba1 + macrophage-like cells were observed in close association with CD31 + capillaries within the mesodermal part of the organoid. ( H ) Iba1 + cells were also found within the neural part of the organoid being tightly associated with TUJ1 + neurons suggesting a microglia-like identity. ( I ) Microglia-like cells show a cellular morphology similar to microglial cells at the transition from an amoeboid to a ramified appearance. ( A , B , F , G , H ) Show maximum intensity projections of whole-mount stained cleared organoids. ( C , D , E , I) show stained paraffin sections.

Journal: Scientific Reports

Article Title: Generation of complex human organoid models including vascular networks by incorporation of mesodermal progenitor cells

doi: 10.1038/s41598-019-52204-7

Figure Lengend Snippet: Vascularization of the neural part of the organoid and invasion of microglia-like cells. ( A ) At day 180 a CD31 + endothelial network infiltrating the Pax6 + neural part of the organoid was observed. ( B ) shows a higher magnification of A. ( C ) Infiltrating vessels were found within the neural tissue surrounding Sox1 + neuroepithelial structures. ( D – E ) CD31 + capillaries within the neural part of the organoid closely associated with GFAP + astrocytes/radial glia and TUJ1 + neurons. ( F ) GFAP + cells form close contacts with CD31 + endothelial cells (see inset). ( G ) Iba1 + macrophage-like cells were observed in close association with CD31 + capillaries within the mesodermal part of the organoid. ( H ) Iba1 + cells were also found within the neural part of the organoid being tightly associated with TUJ1 + neurons suggesting a microglia-like identity. ( I ) Microglia-like cells show a cellular morphology similar to microglial cells at the transition from an amoeboid to a ramified appearance. ( A , B , F , G , H ) Show maximum intensity projections of whole-mount stained cleared organoids. ( C , D , E , I) show stained paraffin sections.

Article Snippet: Primary antibodies to TUJ1 (Biozol, 801202), GFAP (DAKO, Z0334), CD31 (DAKO, M0823), Iba1 (WAKO, 019-19741), Sox1 (R&D Systems, AF3369), Pax6 (Biolegend, 901301), Brachyury (T) (R&D Systems, AF2085), MAP2 (Abcam, AB32454), N-Cadherin (Sigma-Aldrich, C3865) and NG2 (Merck-Millipore, AB5320) were used.

Techniques: Staining