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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.
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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CD19 CAR + T cells were spiked into a whole blood sample from a healthy donor and isolated using the MACSprep™ CD19 CAR MicroBead Kit, one LS Column, one MS Column, a MACSmix™ Tube Rotator, and a QuadroMACS™ Separator. Cells were fluorescently stained with CD19 CAR Detection Reagent, human, Biotin, Biotin Antibody-PE, CD45-VioBlue ®, 7-AAD Staining Solution, CD3-FITC, and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris and dead cells were excluded from the analysis based on scatter signals and 7-AAD fluorescence. The purity of CD19 CAR + T cells after separation is defined by the percentage of CD19 CAR + T cells (viable CD45 dim/+, 7-AAD – cells). The purity of CD19 CAR + T cells varies due to the variation of human samples, experimental set-up, and starting frequency of CD19 CAR + T cells. |
Before separation | |
Figure 2CD19 CAR + T cells were spiked into a whole blood sample from a healthy donor and isolated using the MACSprep™ CD19 CAR MicroBead Kit, one LS Column, one MS Column, a MACSmix™ Tube Rotator, and a QuadroMACS™ Separator. Cells were fluorescently stained with CD19 CAR Detection Reagent, human, Biotin, Biotin Antibody-PE, CD45-VioBlue ®, 7-AAD Staining Solution, CD3-FITC, and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris and dead cells were excluded from the analysis based on scatter signals and 7-AAD fluorescence. The purity of CD19 CAR + T cells after separation is defined by the percentage of CD19 CAR + T cells (viable CD45 dim/+, 7-AAD – cells). The purity of CD19 CAR + T cells varies due to the variation of human samples, experimental set-up, and starting frequency of CD19 CAR + T cells. | |
After separation with one column | After separation with two columns |
Figure 2CD19 CAR + T cells were spiked into a whole blood sample from a healthy donor and isolated using the MACSprep™ CD19 CAR MicroBead Kit, one LS Column, one MS Column, a MACSmix™ Tube Rotator, and a QuadroMACS™ Separator. Cells were fluorescently stained with CD19 CAR Detection Reagent, human, Biotin, Biotin Antibody-PE, CD45-VioBlue ®, 7-AAD Staining Solution, CD3-FITC, and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris and dead cells were excluded from the analysis based on scatter signals and 7-AAD fluorescence. The purity of CD19 CAR + T cells after separation is defined by the percentage of CD19 CAR + T cells (viable CD45 dim/+, 7-AAD – cells). The purity of CD19 CAR + T cells varies due to the variation of human samples, experimental set-up, and starting frequency of CD19 CAR + T cells. | Figure 2CD19 CAR + T cells were spiked into a whole blood sample from a healthy donor and isolated using the MACSprep™ CD19 CAR MicroBead Kit, one LS Column, one MS Column, a MACSmix™ Tube Rotator, and a QuadroMACS™ Separator. Cells were fluorescently stained with CD19 CAR Detection Reagent, human, Biotin, Biotin Antibody-PE, CD45-VioBlue ®, 7-AAD Staining Solution, CD3-FITC, and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris and dead cells were excluded from the analysis based on scatter signals and 7-AAD fluorescence. The purity of CD19 CAR + T cells after separation is defined by the percentage of CD19 CAR + T cells (viable CD45 dim/+, 7-AAD – cells). The purity of CD19 CAR + T cells varies due to the variation of human samples, experimental set-up, and starting frequency of CD19 CAR + T cells. |
CD19 CAR + T cells were spiked into a whole blood sample from a healthy donor and isolated using the MACSprep™ CD19 CAR MicroBead Kit, one LS Column, one MS Column, a MACSmix™ Tube Rotator, and a QuadroMACS™ Separator. Cells were fluorescently stained with CD19 CAR Detection Reagent, human, Biotin, Biotin Antibody-PE, CD45-VioBlue ®, 7-AAD Staining Solution, CD3-FITC, and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris and dead cells were excluded from the analysis based on scatter signals and 7-AAD fluorescence. The purity of CD19 CAR + T cells after separation is defined by the percentage of CD19 CAR + T cells (viable CD45 dim/+, 7-AAD – cells). The purity of CD19 CAR + T cells varies due to the variation of human samples, experimental set-up, and starting frequency of CD19 CAR + T cells. |
Before separation | |
Figure 2CD19 CAR + T cells were spiked into a whole blood sample from a healthy donor and isolated using the MACSprep™ CD19 CAR MicroBead Kit, one LS Column, one MS Column, a MACSmix™ Tube Rotator, and a QuadroMACS™ Separator. Cells were fluorescently stained with CD19 CAR Detection Reagent, human, Biotin, Biotin Antibody-PE, CD45-VioBlue ®, 7-AAD Staining Solution, CD3-FITC, and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris and dead cells were excluded from the analysis based on scatter signals and 7-AAD fluorescence. The purity of CD19 CAR + T cells after separation is defined by the percentage of CD19 CAR + T cells (viable CD45 dim/+, 7-AAD – cells). The purity of CD19 CAR + T cells varies due to the variation of human samples, experimental set-up, and starting frequency of CD19 CAR + T cells. | |
After separation with one column | After separation with two columns |
Figure 2CD19 CAR + T cells were spiked into a whole blood sample from a healthy donor and isolated using the MACSprep™ CD19 CAR MicroBead Kit, one LS Column, one MS Column, a MACSmix™ Tube Rotator, and a QuadroMACS™ Separator. Cells were fluorescently stained with CD19 CAR Detection Reagent, human, Biotin, Biotin Antibody-PE, CD45-VioBlue ®, 7-AAD Staining Solution, CD3-FITC, and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris and dead cells were excluded from the analysis based on scatter signals and 7-AAD fluorescence. The purity of CD19 CAR + T cells after separation is defined by the percentage of CD19 CAR + T cells (viable CD45 dim/+, 7-AAD – cells). The purity of CD19 CAR + T cells varies due to the variation of human samples, experimental set-up, and starting frequency of CD19 CAR + T cells. | Figure 2CD19 CAR + T cells were spiked into a whole blood sample from a healthy donor and isolated using the MACSprep™ CD19 CAR MicroBead Kit, one LS Column, one MS Column, a MACSmix™ Tube Rotator, and a QuadroMACS™ Separator. Cells were fluorescently stained with CD19 CAR Detection Reagent, human, Biotin, Biotin Antibody-PE, CD45-VioBlue ®, 7-AAD Staining Solution, CD3-FITC, and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris and dead cells were excluded from the analysis based on scatter signals and 7-AAD fluorescence. The purity of CD19 CAR + T cells after separation is defined by the percentage of CD19 CAR + T cells (viable CD45 dim/+, 7-AAD – cells). The purity of CD19 CAR + T cells varies due to the variation of human samples, experimental set-up, and starting frequency of CD19 CAR + T cells. |
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