endothelial cell growth medium mv2 kit with supplement pack Search Results


endothelial cell growth medium mv2  (Innoprot Inc)
95
Innoprot Inc endothelial cell growth medium mv2
Endothelial Cell Growth Medium Mv2, supplied by Innoprot Inc, 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/endothelial+cell+growth+medium+mv2+kit+with+supplement+pack/Endothelial+Cell+Medium+Kit/pmc12806495-59-60-72
Average 95 stars, based on 1 article reviews
endothelial cell growth medium mv2 - by Bioz Stars, 2026-09
95/100 stars
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c-22121  (promocell)
96
promocell c-22121
KEY RESOURCES TABLE
C 22121, supplied by promocell, 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/endothelial+cell+growth+medium+mv2+kit+with+supplement+pack/Endothelial+Cell+Growth+Medium+MV+2+Kit/pmc09498980-36-0-7
Average 96 stars, based on 1 article reviews
c-22121 - by Bioz Stars, 2026-09
96/100 stars
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collagen type i  (Corning Life Sciences)
90
Corning Life Sciences collagen type i
KEY RESOURCES TABLE
Collagen Type I, supplied by Corning Life Sciences, 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/endothelial+cell+growth+medium+mv2+kit+with+supplement+pack/collagen+type+i/pmc07101077-182-13-17
Average 90 stars, based on 1 article reviews
collagen type i - by Bioz Stars, 2026-09
90/100 stars
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cd31 microbead kit  (Miltenyi Biotec)
96
Miltenyi Biotec cd31 microbead kit
A . Schematic illustration of BMEC differentiation protocol. B . Morphological changes of iPSC during BMEC differentiation under light microscope. C . Immunofluorescent staining of BMEC marker proteins, including adherence junction proteins <t>(CD31,</t> VE-cadherine), tight junction proteins (Occludin, claudin 5, ZO-1), and glucose transporter, Glut-1. Scale bars, 100 µm. D . IPSC-BMECs at day 10 differentiation were treated with the Dil-ac-LDL dye and visualised under fluorescent microscope. Scale bar, 200 µm. E . In vitro angiogenesis assay on Matrigel. Scale bar, 200 µm. F . Schematic illustration of the in vitro NVU using Transwell setting. The BBB function is measured as TEER values using a Voltmeter. G . IPSC-BMECs, iPSC-ECs and hCAECs were seeded on to the insert of the Transwell, respectively. TEER values were measured each day for five consecutive days (120 h). Data are represented as mean ± SEM, n=3. Two-way ANOVA with Tukey’s post hoc test, *p<0.05, **p<0.01. Figure F was created using BioRender.
Cd31 Microbead Kit, supplied by Miltenyi Biotec, 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/endothelial+cell+growth+medium+mv2+kit+with+supplement+pack/CD31+MicroBead+Kit%2C+human/bio_rxiv__2023__04__26__538393-77-9-12
Average 96 stars, based on 1 article reviews
cd31 microbead kit - by Bioz Stars, 2026-09
96/100 stars
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matrigeltm  (Corning Life Sciences)
90
Corning Life Sciences matrigeltm
A . Schematic illustration of BMEC differentiation protocol. B . Morphological changes of iPSC during BMEC differentiation under light microscope. C . Immunofluorescent staining of BMEC marker proteins, including adherence junction proteins <t>(CD31,</t> VE-cadherine), tight junction proteins (Occludin, claudin 5, ZO-1), and glucose transporter, Glut-1. Scale bars, 100 µm. D . IPSC-BMECs at day 10 differentiation were treated with the Dil-ac-LDL dye and visualised under fluorescent microscope. Scale bar, 200 µm. E . In vitro angiogenesis assay on Matrigel. Scale bar, 200 µm. F . Schematic illustration of the in vitro NVU using Transwell setting. The BBB function is measured as TEER values using a Voltmeter. G . IPSC-BMECs, iPSC-ECs and hCAECs were seeded on to the insert of the Transwell, respectively. TEER values were measured each day for five consecutive days (120 h). Data are represented as mean ± SEM, n=3. Two-way ANOVA with Tukey’s post hoc test, *p<0.05, **p<0.01. Figure F was created using BioRender.
Matrigeltm, supplied by Corning Life Sciences, 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/endothelial+cell+growth+medium+mv2+kit+with+supplement+pack/matrigeltm/pmc07101077-182-11-17
Average 90 stars, based on 1 article reviews
matrigeltm - by Bioz Stars, 2026-09
90/100 stars
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rneasy plus mini kit  (Qiagen)
99
Qiagen rneasy plus mini kit
A . Schematic illustration of BMEC differentiation protocol. B . Morphological changes of iPSC during BMEC differentiation under light microscope. C . Immunofluorescent staining of BMEC marker proteins, including adherence junction proteins <t>(CD31,</t> VE-cadherine), tight junction proteins (Occludin, claudin 5, ZO-1), and glucose transporter, Glut-1. Scale bars, 100 µm. D . IPSC-BMECs at day 10 differentiation were treated with the Dil-ac-LDL dye and visualised under fluorescent microscope. Scale bar, 200 µm. E . In vitro angiogenesis assay on Matrigel. Scale bar, 200 µm. F . Schematic illustration of the in vitro NVU using Transwell setting. The BBB function is measured as TEER values using a Voltmeter. G . IPSC-BMECs, iPSC-ECs and hCAECs were seeded on to the insert of the Transwell, respectively. TEER values were measured each day for five consecutive days (120 h). Data are represented as mean ± SEM, n=3. Two-way ANOVA with Tukey’s post hoc test, *p<0.05, **p<0.01. Figure F was created using BioRender.
Rneasy Plus Mini Kit, supplied by Qiagen, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/endothelial+cell+growth+medium+mv2+kit+with+supplement+pack/RNeasy+Plus+Mini+Kit/pmc10987886-106-51-55
Average 99 stars, based on 1 article reviews
rneasy plus mini kit - by Bioz Stars, 2026-09
99/100 stars
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matrigel™  (Corning Life Sciences)
90
Corning Life Sciences matrigel™
A . Schematic illustration of BMEC differentiation protocol. B . Morphological changes of iPSC during BMEC differentiation under light microscope. C . Immunofluorescent staining of BMEC marker proteins, including adherence junction proteins <t>(CD31,</t> VE-cadherine), tight junction proteins (Occludin, claudin 5, ZO-1), and glucose transporter, Glut-1. Scale bars, 100 µm. D . IPSC-BMECs at day 10 differentiation were treated with the Dil-ac-LDL dye and visualised under fluorescent microscope. Scale bar, 200 µm. E . In vitro angiogenesis assay on Matrigel. Scale bar, 200 µm. F . Schematic illustration of the in vitro NVU using Transwell setting. The BBB function is measured as TEER values using a Voltmeter. G . IPSC-BMECs, iPSC-ECs and hCAECs were seeded on to the insert of the Transwell, respectively. TEER values were measured each day for five consecutive days (120 h). Data are represented as mean ± SEM, n=3. Two-way ANOVA with Tukey’s post hoc test, *p<0.05, **p<0.01. Figure F was created using BioRender.
Matrigel™, supplied by Corning Life Sciences, 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/endothelial+cell+growth+medium+mv2+kit+with+supplement+pack/matrigel/pmc07101077-100-14-20
Average 90 stars, based on 1 article reviews
matrigel™ - by Bioz Stars, 2026-09
90/100 stars
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qiashredder  (Qiagen)
99
Qiagen qiashredder
A . Schematic illustration of BMEC differentiation protocol. B . Morphological changes of iPSC during BMEC differentiation under light microscope. C . Immunofluorescent staining of BMEC marker proteins, including adherence junction proteins <t>(CD31,</t> VE-cadherine), tight junction proteins (Occludin, claudin 5, ZO-1), and glucose transporter, Glut-1. Scale bars, 100 µm. D . IPSC-BMECs at day 10 differentiation were treated with the Dil-ac-LDL dye and visualised under fluorescent microscope. Scale bar, 200 µm. E . In vitro angiogenesis assay on Matrigel. Scale bar, 200 µm. F . Schematic illustration of the in vitro NVU using Transwell setting. The BBB function is measured as TEER values using a Voltmeter. G . IPSC-BMECs, iPSC-ECs and hCAECs were seeded on to the insert of the Transwell, respectively. TEER values were measured each day for five consecutive days (120 h). Data are represented as mean ± SEM, n=3. Two-way ANOVA with Tukey’s post hoc test, *p<0.05, **p<0.01. Figure F was created using BioRender.
Qiashredder, supplied by Qiagen, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/endothelial+cell+growth+medium+mv2+kit+with+supplement+pack/QIAshredder/pmc10987886-106-59-60
Average 99 stars, based on 1 article reviews
qiashredder - by Bioz Stars, 2026-09
99/100 stars
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t75 corning cellbind flasks  (Corning Life Sciences)
90
Corning Life Sciences t75 corning cellbind flasks
A . Schematic illustration of BMEC differentiation protocol. B . Morphological changes of iPSC during BMEC differentiation under light microscope. C . Immunofluorescent staining of BMEC marker proteins, including adherence junction proteins <t>(CD31,</t> VE-cadherine), tight junction proteins (Occludin, claudin 5, ZO-1), and glucose transporter, Glut-1. Scale bars, 100 µm. D . IPSC-BMECs at day 10 differentiation were treated with the Dil-ac-LDL dye and visualised under fluorescent microscope. Scale bar, 200 µm. E . In vitro angiogenesis assay on Matrigel. Scale bar, 200 µm. F . Schematic illustration of the in vitro NVU using Transwell setting. The BBB function is measured as TEER values using a Voltmeter. G . IPSC-BMECs, iPSC-ECs and hCAECs were seeded on to the insert of the Transwell, respectively. TEER values were measured each day for five consecutive days (120 h). Data are represented as mean ± SEM, n=3. Two-way ANOVA with Tukey’s post hoc test, *p<0.05, **p<0.01. Figure F was created using BioRender.
T75 Corning Cellbind Flasks, supplied by Corning Life Sciences, 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/endothelial+cell+growth+medium+mv2+kit+with+supplement+pack/96+well+plates/pm33038299-56-49-50
Average 90 stars, based on 1 article reviews
t75 corning cellbind flasks - by Bioz Stars, 2026-09
90/100 stars
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phenol-free matrigel 356237  (Corning Life Sciences)
90
Corning Life Sciences phenol-free matrigel 356237
A . Schematic illustration of BMEC differentiation protocol. B . Morphological changes of iPSC during BMEC differentiation under light microscope. C . Immunofluorescent staining of BMEC marker proteins, including adherence junction proteins <t>(CD31,</t> VE-cadherine), tight junction proteins (Occludin, claudin 5, ZO-1), and glucose transporter, Glut-1. Scale bars, 100 µm. D . IPSC-BMECs at day 10 differentiation were treated with the Dil-ac-LDL dye and visualised under fluorescent microscope. Scale bar, 200 µm. E . In vitro angiogenesis assay on Matrigel. Scale bar, 200 µm. F . Schematic illustration of the in vitro NVU using Transwell setting. The BBB function is measured as TEER values using a Voltmeter. G . IPSC-BMECs, iPSC-ECs and hCAECs were seeded on to the insert of the Transwell, respectively. TEER values were measured each day for five consecutive days (120 h). Data are represented as mean ± SEM, n=3. Two-way ANOVA with Tukey’s post hoc test, *p<0.05, **p<0.01. Figure F was created using BioRender.
Phenol Free Matrigel 356237, supplied by Corning Life Sciences, 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/endothelial+cell+growth+medium+mv2+kit+with+supplement+pack/matrigel+basement+membrane+matrix+phenol+red+free+356237/pmc09431695-185-11-13
Average 90 stars, based on 1 article reviews
phenol-free matrigel 356237 - by Bioz Stars, 2026-09
90/100 stars
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cd34 microbead kit  (Miltenyi Biotec)
97
Miltenyi Biotec cd34 microbead kit
A . Schematic illustration of BMEC differentiation protocol. B . Morphological changes of iPSC during BMEC differentiation under light microscope. C . Immunofluorescent staining of BMEC marker proteins, including adherence junction proteins <t>(CD31,</t> VE-cadherine), tight junction proteins (Occludin, claudin 5, ZO-1), and glucose transporter, Glut-1. Scale bars, 100 µm. D . IPSC-BMECs at day 10 differentiation were treated with the Dil-ac-LDL dye and visualised under fluorescent microscope. Scale bar, 200 µm. E . In vitro angiogenesis assay on Matrigel. Scale bar, 200 µm. F . Schematic illustration of the in vitro NVU using Transwell setting. The BBB function is measured as TEER values using a Voltmeter. G . IPSC-BMECs, iPSC-ECs and hCAECs were seeded on to the insert of the Transwell, respectively. TEER values were measured each day for five consecutive days (120 h). Data are represented as mean ± SEM, n=3. Two-way ANOVA with Tukey’s post hoc test, *p<0.05, **p<0.01. Figure F was created using BioRender.
Cd34 Microbead Kit, supplied by Miltenyi Biotec, 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/endothelial+cell+growth+medium+mv2+kit+with+supplement+pack/CD34+MicroBead+Kit%2C+human/pmc08457614-117-14-24
Average 97 stars, based on 1 article reviews
cd34 microbead kit - by Bioz Stars, 2026-09
97/100 stars
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human abdominal aortic ecs (haaecs)  (Coriell Institute for Medical Research)
90
Coriell Institute for Medical Research human abdominal aortic ecs (haaecs)
A . Schematic illustration of BMEC differentiation protocol. B . Morphological changes of iPSC during BMEC differentiation under light microscope. C . Immunofluorescent staining of BMEC marker proteins, including adherence junction proteins <t>(CD31,</t> VE-cadherine), tight junction proteins (Occludin, claudin 5, ZO-1), and glucose transporter, Glut-1. Scale bars, 100 µm. D . IPSC-BMECs at day 10 differentiation were treated with the Dil-ac-LDL dye and visualised under fluorescent microscope. Scale bar, 200 µm. E . In vitro angiogenesis assay on Matrigel. Scale bar, 200 µm. F . Schematic illustration of the in vitro NVU using Transwell setting. The BBB function is measured as TEER values using a Voltmeter. G . IPSC-BMECs, iPSC-ECs and hCAECs were seeded on to the insert of the Transwell, respectively. TEER values were measured each day for five consecutive days (120 h). Data are represented as mean ± SEM, n=3. Two-way ANOVA with Tukey’s post hoc test, *p<0.05, **p<0.01. Figure F was created using BioRender.
Human Abdominal Aortic Ecs (Haaecs), supplied by Coriell Institute for Medical Research, 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/endothelial+cell+growth+medium+mv2+kit+with+supplement+pack/human+abdominal+aortic+endothelial+cells++haaecs+/pm26414399-64-0-5
Average 90 stars, based on 1 article reviews
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Image Search Results


KEY RESOURCES TABLE

Journal: Cell reports

Article Title: Genetic- and diet-induced ω -3 fatty acid enrichment enhances TRPV4-mediated vasodilation in mice

doi: 10.1016/j.celrep.2022.111306

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: Endothelial Cell Growth Medium MV 2 , Promo Cell , C-22121.

Techniques: Recombinant, Protease Inhibitor, Staining, Western Blot, Membrane, Protein Extraction, Plasmid Preparation, Software, Imaging, Microscopy

A . Schematic illustration of BMEC differentiation protocol. B . Morphological changes of iPSC during BMEC differentiation under light microscope. C . Immunofluorescent staining of BMEC marker proteins, including adherence junction proteins (CD31, VE-cadherine), tight junction proteins (Occludin, claudin 5, ZO-1), and glucose transporter, Glut-1. Scale bars, 100 µm. D . IPSC-BMECs at day 10 differentiation were treated with the Dil-ac-LDL dye and visualised under fluorescent microscope. Scale bar, 200 µm. E . In vitro angiogenesis assay on Matrigel. Scale bar, 200 µm. F . Schematic illustration of the in vitro NVU using Transwell setting. The BBB function is measured as TEER values using a Voltmeter. G . IPSC-BMECs, iPSC-ECs and hCAECs were seeded on to the insert of the Transwell, respectively. TEER values were measured each day for five consecutive days (120 h). Data are represented as mean ± SEM, n=3. Two-way ANOVA with Tukey’s post hoc test, *p<0.05, **p<0.01. Figure F was created using BioRender.

Journal: bioRxiv

Article Title: Induced pluripotent stem cell model revealed impaired neurovascular interaction in genetic small vessel disease CADASIL

doi: 10.1101/2023.04.26.538393

Figure Lengend Snippet: A . Schematic illustration of BMEC differentiation protocol. B . Morphological changes of iPSC during BMEC differentiation under light microscope. C . Immunofluorescent staining of BMEC marker proteins, including adherence junction proteins (CD31, VE-cadherine), tight junction proteins (Occludin, claudin 5, ZO-1), and glucose transporter, Glut-1. Scale bars, 100 µm. D . IPSC-BMECs at day 10 differentiation were treated with the Dil-ac-LDL dye and visualised under fluorescent microscope. Scale bar, 200 µm. E . In vitro angiogenesis assay on Matrigel. Scale bar, 200 µm. F . Schematic illustration of the in vitro NVU using Transwell setting. The BBB function is measured as TEER values using a Voltmeter. G . IPSC-BMECs, iPSC-ECs and hCAECs were seeded on to the insert of the Transwell, respectively. TEER values were measured each day for five consecutive days (120 h). Data are represented as mean ± SEM, n=3. Two-way ANOVA with Tukey’s post hoc test, *p<0.05, **p<0.01. Figure F was created using BioRender.

Article Snippet: On day 12, endothelial cells were purified using a CD31 MicroBead Kit (Miltenyi Biotec, 130-091-935) and further cultured in the Promocell endothelial cell medium (MV2) until use.

Techniques: Light Microscopy, Staining, Marker, Microscopy, In Vitro, Angiogenesis Assay