human endothelial cell culture medium Search Results


rat brain microvascular endothelial cell growth media  (Cell Applications Inc)
96
Cell Applications Inc rat brain microvascular endothelial cell growth media
Figure 3 Three hours of hypoxia and 6 h of reperfusion lead to significant <t>endothelial</t> cell death in vitro in rat brain <t>microvascular</t> endothelial cells (RBMVEC; A). Non-specific gap junction blocker carbenoxolone, non-specific hemichannel blocker LaCl3, and connexin43 (Cx43) mimetic peptide protected endothelial cells against hypoxic injury, with the number of viable cells significantly higher than no treatment, while scrambled peptide did not have any protective effects. The number of viable cells was expressed as percentage of the control without hypoxia. Hypoxia and reperfusion also lead to significant propidium iodide dye uptake into primary rat brain microvascular endothelial cells indicating open hemichannels (B). Carbenoxolone, LaCl3 and connexin43 mimetic peptide significantly prevented dye uptake compared to no treatment, indicating hemichannel closure, while scrambled peptide did not have any effect. Stars denote statistical significance when compared to the control group or compared between groups in brackets; P 5 0.05.
Rat Brain Microvascular Endothelial Cell Growth Media, supplied by Cell Applications 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/result/rat brain microvascular endothelial cell growth media/product/Cell Applications Inc
Average 96 stars, based on 1 article reviews
rat brain microvascular endothelial cell growth media - by Bioz Stars, 2026-03
96/100 stars
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human umbilical cord endothelial cell culture medium  (Lonza)
90
Lonza human umbilical cord endothelial cell culture medium
( A ) CIA1 and CIA2 reduced <t>cell</t> growth of prostate cancer cells. Cell viability was measured 96 hours after CIA1 or CIA2 treatment. n = 3 per group. ( B ) CIA1 and CIA2 reduced colony formation ability of prostate cancer cells. PC3 cells were treated with inhibitor for 12 days. n = 3 per group. Two-way analysis of variance (ANOVA). ( C ) CIA1 and CIA2 reduced prostate cancer cell invasion. PC3 cells were treated with 1 μM CIA1 or CIA2 for 48 hours. Invasion was measured by transwell assay. n = 3 per group. One-way ANOVA. DMSO, dimethyl sulfoxide. ( D ) Angiogenesis was measured by <t>human</t> <t>umbilical</t> <t>cord</t> <t>endothelial</t> cell sprouting assay. n = 3 per group. One-way ANOVA. *** P < 0.001.
Human Umbilical Cord Endothelial Cell Culture Medium, supplied by Lonza, 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/result/human umbilical cord endothelial cell culture medium/product/Lonza
Average 90 stars, based on 1 article reviews
human umbilical cord endothelial cell culture medium - by Bioz Stars, 2026-03
90/100 stars
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human endothelial cell culture medium  (Nissui Pharmaceutical)
90
Nissui Pharmaceutical human endothelial cell culture medium
( A ) CIA1 and CIA2 reduced <t>cell</t> growth of prostate cancer cells. Cell viability was measured 96 hours after CIA1 or CIA2 treatment. n = 3 per group. ( B ) CIA1 and CIA2 reduced colony formation ability of prostate cancer cells. PC3 cells were treated with inhibitor for 12 days. n = 3 per group. Two-way analysis of variance (ANOVA). ( C ) CIA1 and CIA2 reduced prostate cancer cell invasion. PC3 cells were treated with 1 μM CIA1 or CIA2 for 48 hours. Invasion was measured by transwell assay. n = 3 per group. One-way ANOVA. DMSO, dimethyl sulfoxide. ( D ) Angiogenesis was measured by <t>human</t> <t>umbilical</t> <t>cord</t> <t>endothelial</t> cell sprouting assay. n = 3 per group. One-way ANOVA. *** P < 0.001.
Human Endothelial Cell Culture Medium, supplied by Nissui Pharmaceutical, 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/result/human endothelial cell culture medium/product/Nissui Pharmaceutical
Average 90 stars, based on 1 article reviews
human endothelial cell culture medium - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

Image Search Results


Figure 3 Three hours of hypoxia and 6 h of reperfusion lead to significant endothelial cell death in vitro in rat brain microvascular endothelial cells (RBMVEC; A). Non-specific gap junction blocker carbenoxolone, non-specific hemichannel blocker LaCl3, and connexin43 (Cx43) mimetic peptide protected endothelial cells against hypoxic injury, with the number of viable cells significantly higher than no treatment, while scrambled peptide did not have any protective effects. The number of viable cells was expressed as percentage of the control without hypoxia. Hypoxia and reperfusion also lead to significant propidium iodide dye uptake into primary rat brain microvascular endothelial cells indicating open hemichannels (B). Carbenoxolone, LaCl3 and connexin43 mimetic peptide significantly prevented dye uptake compared to no treatment, indicating hemichannel closure, while scrambled peptide did not have any effect. Stars denote statistical significance when compared to the control group or compared between groups in brackets; P 5 0.05.

Journal: Brain : a journal of neurology

Article Title: Connexin43 mimetic peptide reduces vascular leak and retinal ganglion cell death following retinal ischaemia.

doi: 10.1093/brain/awr338

Figure Lengend Snippet: Figure 3 Three hours of hypoxia and 6 h of reperfusion lead to significant endothelial cell death in vitro in rat brain microvascular endothelial cells (RBMVEC; A). Non-specific gap junction blocker carbenoxolone, non-specific hemichannel blocker LaCl3, and connexin43 (Cx43) mimetic peptide protected endothelial cells against hypoxic injury, with the number of viable cells significantly higher than no treatment, while scrambled peptide did not have any protective effects. The number of viable cells was expressed as percentage of the control without hypoxia. Hypoxia and reperfusion also lead to significant propidium iodide dye uptake into primary rat brain microvascular endothelial cells indicating open hemichannels (B). Carbenoxolone, LaCl3 and connexin43 mimetic peptide significantly prevented dye uptake compared to no treatment, indicating hemichannel closure, while scrambled peptide did not have any effect. Stars denote statistical significance when compared to the control group or compared between groups in brackets; P 5 0.05.

Article Snippet: Rat brain microvascular endothelial cells (R840K-05a, Cell Applications) were plated into 24-well plates (1 105 cells/well) in rat brain microvascular endothelial cell growth media (R819K-500, Cell Applications) and allowed to settle for 16 h. Medium was then removed and replaced with Dulbecco’s Modified Eagle’s Medium/F12 containing 0.5% foetal bovine serum and 1% glutamine.

Techniques: In Vitro, Control

( A ) CIA1 and CIA2 reduced cell growth of prostate cancer cells. Cell viability was measured 96 hours after CIA1 or CIA2 treatment. n = 3 per group. ( B ) CIA1 and CIA2 reduced colony formation ability of prostate cancer cells. PC3 cells were treated with inhibitor for 12 days. n = 3 per group. Two-way analysis of variance (ANOVA). ( C ) CIA1 and CIA2 reduced prostate cancer cell invasion. PC3 cells were treated with 1 μM CIA1 or CIA2 for 48 hours. Invasion was measured by transwell assay. n = 3 per group. One-way ANOVA. DMSO, dimethyl sulfoxide. ( D ) Angiogenesis was measured by human umbilical cord endothelial cell sprouting assay. n = 3 per group. One-way ANOVA. *** P < 0.001.

Journal: Science Advances

Article Title: Small-molecule inhibitor targeting orphan nuclear receptor COUP-TFII for prostate cancer treatment

doi: 10.1126/sciadv.aaz8031

Figure Lengend Snippet: ( A ) CIA1 and CIA2 reduced cell growth of prostate cancer cells. Cell viability was measured 96 hours after CIA1 or CIA2 treatment. n = 3 per group. ( B ) CIA1 and CIA2 reduced colony formation ability of prostate cancer cells. PC3 cells were treated with inhibitor for 12 days. n = 3 per group. Two-way analysis of variance (ANOVA). ( C ) CIA1 and CIA2 reduced prostate cancer cell invasion. PC3 cells were treated with 1 μM CIA1 or CIA2 for 48 hours. Invasion was measured by transwell assay. n = 3 per group. One-way ANOVA. DMSO, dimethyl sulfoxide. ( D ) Angiogenesis was measured by human umbilical cord endothelial cell sprouting assay. n = 3 per group. One-way ANOVA. *** P < 0.001.

Article Snippet: Human umbilical cord endothelial cell culture medium was from Lonza (CC-3162, Lonza, Basel, Switzerland).

Techniques: Transwell Assay