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Miltenyi Biotec B.V.
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As a global market leader with numerous subsidiaries and distributors, Miltenyi Biotec is committed to providing our customers around the world with the highest quality products. In addition to direct selling in more than 20 countries in North America, Europe and Asia/Pacific, Miltenyi Biotec also provides support for our customers through an extensive distributor network covering dozens of additional countries.
Our local employees are always happy to answer your questions. Highly trained and experienced teams in your country can provide quick, helpful, and comprehensive support.
Miltenyi Biotec B.V.
Sandifortdreef 17
2333 ZZ Leiden
The Netherlands
Phone: 0800 94016
Fax: 0800 99626
E-Mail: macs@miltenyibiotec.nl
Web: www.miltenyibiotec.com
For immediate technical support, use our live chat. Connect with us
As a global market leader with numerous subsidiaries and distributors, Miltenyi Biotec is committed to providing our customers around the world with the highest quality products. In addition to direct selling in more than 20 countries in North America, Europe and Asia/Pacific, Miltenyi Biotec also provides support for our customers through an extensive distributor network covering dozens of additional countries.
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Cardiac endothelial cells were isolated from P1 Wistar rat hearts by using the Neonatal Cardiac Endothelial Cell Isolation Kit, one LD column with MidiMACS Separator and one MS column with MiniMACS Separator. The cells were fluorescently stained with CD90.1-PE (#130-102-636) and CD31-APC (#130-105-937 ) and analyzed by flow cytometry using the MACSQuant Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Neonatal Cardiac Endothelial Cell Isolation Kit, ratFigure 1Cardiac endothelial cells were isolated from P1 Wistar rat hearts by using the Neonatal Cardiac Endothelial Cell Isolation Kit, one LD column with MidiMACS Separator and one MS column with MiniMACS Separator. The cells were fluorescently stained with CD90.1-PE (#130-102-636) and CD31-APC (#130-105-937 ) and analyzed by flow cytometry using the MACSQuant Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Neonatal Cardiac Endothelial Cell Isolation Kit, ratFigure 1Cardiac endothelial cells were isolated from P1 Wistar rat hearts by using the Neonatal Cardiac Endothelial Cell Isolation Kit, one LD column with MidiMACS Separator and one MS column with MiniMACS Separator. The cells were fluorescently stained with CD90.1-PE (#130-102-636) and CD31-APC (#130-105-937 ) and analyzed by flow cytometry using the MACSQuant Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Cardiac endothelial cells were isolated from P1 Wistar rat hearts by using the Neonatal Cardiac Endothelial Cell Isolation Kit, one LD column with MidiMACS Separator and one MS column with MiniMACS Separator. The cells were fluorescently stained with CD90.1-PE (#130-102-636) and CD31-APC (#130-105-937 ) and analyzed by flow cytometry using the MACSQuant Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Neonatal Cardiac Endothelial Cell Isolation Kit, ratFigure 1Cardiac endothelial cells were isolated from P1 Wistar rat hearts by using the Neonatal Cardiac Endothelial Cell Isolation Kit, one LD column with MidiMACS Separator and one MS column with MiniMACS Separator. The cells were fluorescently stained with CD90.1-PE (#130-102-636) and CD31-APC (#130-105-937 ) and analyzed by flow cytometry using the MACSQuant Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Neonatal Cardiac Endothelial Cell Isolation Kit, ratFigure 1Cardiac endothelial cells were isolated from P1 Wistar rat hearts by using the Neonatal Cardiac Endothelial Cell Isolation Kit, one LD column with MidiMACS Separator and one MS column with MiniMACS Separator. The cells were fluorescently stained with CD90.1-PE (#130-102-636) and CD31-APC (#130-105-937 ) and analyzed by flow cytometry using the MACSQuant Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
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