Alterations of endothelial cells and the vasculature play a central role in the pathogenesis of a broad spectrum of the most dreadful of human diseases, as endothelial cells have the key function of participating in the maintenance of patent and functional capillaries. This makes them a key component for Drug Discovery.
We are proud that Biotech and Biopharma Cos. are increasingly using our cells. We believe we represent the best options. Here're some of the cells currently available:
- Human Bladder Microvascular Endothelial Cells
- Human Cardiac Microvascular Endothelial Cells
- Human Dermal Lymphatic Microvascular Endothelial Cells
- Human Dermal Microvascular Endothelial Cells
- Human Glomerular Microvascular Endothelial Cells
- Human Large Intestine Microvascular Endothelial Cells
- Human Ovarian Microvascular Endothelial Cells
- Human Pancreatic Microvascular Endothelial Cells
- Human Prostate Microvascular Endothelial Cells
- Human Retinal Microvascular Endothelial Cells
- Human Synovial Microvascular Endothelial Cells
- Human Tonsil Microvascular Endothelial Cells
Figures: HRMECs treated with SUZ12 siRNA demonstrate increased miR-200b expression, decreased VEGF expression and decreased endothelial branching. A,B: Gene knockdown of EZH2 and SUZ12 was confirmed by qPCR. C,D: In HRMECs transfected with EZH2 siRNA in HG, miR-200b and VEGF were not significantly different from HG+control siRNA but decreased compared to NG+control siRNA. In HRMECs transfected with SUZ12 siRNA in HG, miR-200b was significantly increased with decreased levels of VEGF compared to HRMECs transfected with control siRNA, with levels similar to NG+control siRNA. E,F: Tube formation assay to measure endothelial branching. HRMECs transfected with HG+control siRNA demonstrated significantly increased branching compared to NG+control siRNA. Transfection of EZH2 siRNA did not reduce endothelial branching significantly compared to HG+control siRNA. However, transfection of SUZ12 siRNA significantly reduced endothelial branching compared to HG+control siRNA. 10.1371/journal.pone.0123987
We will keep you posted as we add more cell options.
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