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Whole Blood CD3 MicroBeads
Description
Whole Blood CD3 MicroBeads were developed for rapid positive selection of CD3+ cells directly from whole blood or bone marrow. No sample preparation is required, including density gradient centrifugation or erythrocyte lysis. Anticoagulated cell samples of 0.25–15 mL are labeled with Whole Blood CD3 MicroBeads to be subsequently separated with the autoMACS™ Pro Separator or the autoMACS Separator, or using the Whole Blood Column Kit.
Whole Blood CD3 MicroBeads recognize the CD3 antigen which is associated with the T cell receptor (TCR) heterodimer. CD3 is expressed on all T cells, constituting 15–20% of human peripheral blood leukocytes.
Applications
Whole Blood MicroBeads allow the fast isolation of CD3+ cells directly from whole blood or bone marrow, thus minimizing hands-on time and maximizing yield of target cells. Whole Blood MicroBeads in combination with the autoMACS™ Separators allow standardization of the cell separation procedure and safe handling of hazardous samples. The purified CD3+ cells are well-suited for further flow cytometric, functional, or molecular analysis including lineage-specific chimerism analysis after allogeneic stem cell transplantation1,2.
For more information on MACS® Whole Blood MicroBeads click here.
Columns
autoMACS™ Columns: autoMACS™ Pro Separator (Program Posselwb; 0.25–15 mL sample volume), or autoMACS Separator (Program Posseld2; 0.25–3 mL sample volume)
Whole Blood Column Kit: for 0.25–15 mL sample volume
 
Figure 1
CD3+ cells were separated from whole blood using Whole Blood CD3 MicroBeads and the autoMACS™ Separator with program Posseld2. Cells were fluorescently stained with CD3-FITC and CD45-PE.
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Whole Blood CD3 MicroBeads, human
For research use only
- for 40 mL whole blood
Download data sheet
130-090-874
Qty:
 

Related products
MACS® Cell Separation from whole blood
autoMACS Pro Starting Kit (#130-092-545)
autoMACS Starting Kit (#201-01)
Whole Blood Column Kit (#130-093-545)
CD3 Antibodies
CD45 Antibodies
MACS® Cell Analysis Reagents
References
1. Köhl et al. (2003) Leukemia 17: 232–236.[2571]
2. Adams et al. (2004) MACS&more 8/2: 16–17.
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