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Miltenyi Biotec distribution:
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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Untouched CD4 + memory T cells were isolated from 30 mL of human EDTA-anticoagulated whole blood using the MACSxpress ® Whole Blood CD4 + Memory T Cell Isolation Kit, a MACSmix™ Tube Rotator, and a MACSxpress Separator. The isolated cells were fluorescently stained with CD45RO-APC, CD4-PE, CD45RA-FITC, and CD45-VioBlue ® and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris, non-leukocytes, and dead cells were excluded from the analysis based on CD45 expression, scatter signals, and propidium iodide fluorescence. CD45RA versus CD45RO expression is shown for gated CD4 + cells. |
Before separation | After separation |
Figure 1Untouched CD4 + memory T cells were isolated from 30 mL of human EDTA-anticoagulated whole blood using the MACSxpress ® Whole Blood CD4 + Memory T Cell Isolation Kit, a MACSmix™ Tube Rotator, and a MACSxpress Separator. The isolated cells were fluorescently stained with CD45RO-APC, CD4-PE, CD45RA-FITC, and CD45-VioBlue ® and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris, non-leukocytes, and dead cells were excluded from the analysis based on CD45 expression, scatter signals, and propidium iodide fluorescence. CD45RA versus CD45RO expression is shown for gated CD4 + cells. | Figure 1Untouched CD4 + memory T cells were isolated from 30 mL of human EDTA-anticoagulated whole blood using the MACSxpress ® Whole Blood CD4 + Memory T Cell Isolation Kit, a MACSmix™ Tube Rotator, and a MACSxpress Separator. The isolated cells were fluorescently stained with CD45RO-APC, CD4-PE, CD45RA-FITC, and CD45-VioBlue ® and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris, non-leukocytes, and dead cells were excluded from the analysis based on CD45 expression, scatter signals, and propidium iodide fluorescence. CD45RA versus CD45RO expression is shown for gated CD4 + cells. |
Figure 1Untouched CD4 + memory T cells were isolated from 30 mL of human EDTA-anticoagulated whole blood using the MACSxpress ® Whole Blood CD4 + Memory T Cell Isolation Kit, a MACSmix™ Tube Rotator, and a MACSxpress Separator. The isolated cells were fluorescently stained with CD45RO-APC, CD4-PE, CD45RA-FITC, and CD45-VioBlue ® and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris, non-leukocytes, and dead cells were excluded from the analysis based on CD45 expression, scatter signals, and propidium iodide fluorescence. CD45RA versus CD45RO expression is shown for gated CD4 + cells. | Figure 1Untouched CD4 + memory T cells were isolated from 30 mL of human EDTA-anticoagulated whole blood using the MACSxpress ® Whole Blood CD4 + Memory T Cell Isolation Kit, a MACSmix™ Tube Rotator, and a MACSxpress Separator. The isolated cells were fluorescently stained with CD45RO-APC, CD4-PE, CD45RA-FITC, and CD45-VioBlue ® and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris, non-leukocytes, and dead cells were excluded from the analysis based on CD45 expression, scatter signals, and propidium iodide fluorescence. CD45RA versus CD45RO expression is shown for gated CD4 + cells. |
Untouched CD4 + memory T cells were isolated from 30 mL of human EDTA-anticoagulated whole blood using the MACSxpress ® Whole Blood CD4 + Memory T Cell Isolation Kit, a MACSmix™ Tube Rotator, and a MACSxpress Separator. The isolated cells were fluorescently stained with CD45RO-APC, CD4-PE, CD45RA-FITC, and CD45-VioBlue ® and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris, non-leukocytes, and dead cells were excluded from the analysis based on CD45 expression, scatter signals, and propidium iodide fluorescence. CD45RA versus CD45RO expression is shown for gated CD4 + cells. |
Before separation | After separation |
Figure 1Untouched CD4 + memory T cells were isolated from 30 mL of human EDTA-anticoagulated whole blood using the MACSxpress ® Whole Blood CD4 + Memory T Cell Isolation Kit, a MACSmix™ Tube Rotator, and a MACSxpress Separator. The isolated cells were fluorescently stained with CD45RO-APC, CD4-PE, CD45RA-FITC, and CD45-VioBlue ® and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris, non-leukocytes, and dead cells were excluded from the analysis based on CD45 expression, scatter signals, and propidium iodide fluorescence. CD45RA versus CD45RO expression is shown for gated CD4 + cells. | Figure 1Untouched CD4 + memory T cells were isolated from 30 mL of human EDTA-anticoagulated whole blood using the MACSxpress ® Whole Blood CD4 + Memory T Cell Isolation Kit, a MACSmix™ Tube Rotator, and a MACSxpress Separator. The isolated cells were fluorescently stained with CD45RO-APC, CD4-PE, CD45RA-FITC, and CD45-VioBlue ® and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris, non-leukocytes, and dead cells were excluded from the analysis based on CD45 expression, scatter signals, and propidium iodide fluorescence. CD45RA versus CD45RO expression is shown for gated CD4 + cells. |
Figure 1Untouched CD4 + memory T cells were isolated from 30 mL of human EDTA-anticoagulated whole blood using the MACSxpress ® Whole Blood CD4 + Memory T Cell Isolation Kit, a MACSmix™ Tube Rotator, and a MACSxpress Separator. The isolated cells were fluorescently stained with CD45RO-APC, CD4-PE, CD45RA-FITC, and CD45-VioBlue ® and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris, non-leukocytes, and dead cells were excluded from the analysis based on CD45 expression, scatter signals, and propidium iodide fluorescence. CD45RA versus CD45RO expression is shown for gated CD4 + cells. | Figure 1Untouched CD4 + memory T cells were isolated from 30 mL of human EDTA-anticoagulated whole blood using the MACSxpress ® Whole Blood CD4 + Memory T Cell Isolation Kit, a MACSmix™ Tube Rotator, and a MACSxpress Separator. The isolated cells were fluorescently stained with CD45RO-APC, CD4-PE, CD45RA-FITC, and CD45-VioBlue ® and analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris, non-leukocytes, and dead cells were excluded from the analysis based on CD45 expression, scatter signals, and propidium iodide fluorescence. CD45RA versus CD45RO expression is shown for gated CD4 + cells. |
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