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  • MACS® Cell Analysis
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Cell separation reagents Cell separation reagents
  for human cells
  for non-human primate cells
  for mouse cells
  for rat cells
  T cells
  B cells
  Dendritic cells
  Antigen-presenting cells
  Neural cells
  for indirect magnetic labeling
  for apoptotic and dead cells
  for isolation of mitochondria
Manual cell separation Manual cell separation
Automated cell separation Automated cell separation
MACS® Technology MACS® Technology
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Anti-T Cell (OX52) MicroBeads
Description
Rat Anti-T Cell (OX52) MicroBeads have been developed for the positive selection or depletion of rat T cells from blood, lymphoid organs, and cell suspensions of non-lymphoid tissues, such as lung or ovary.
Details
Background information
The surface antigen recognized by the MicroBeads is expressed in a lineage-specific manner on thymocytes and T cells. T cells expressing T cell receptor (TCR) α/β as well as TCRγ/δ are recognized. The OX52 antigen is expressed by approximately 1% of bone marrow cells, 99% of thymocytes, 60% of leukocytes in thoracic duct, 60% of lymph node cells, and 30% of splenocytes. The antigen is also weakly expressed on NK cells, which can be distinguished from T cells due to their lack of CD3 or CD5 expression.

Downstream applications
T cells isolated with Anti-T Cell (OX52) MicroBeads can be used for in vitro and in vivo studies on T cell migration and differentiation in the context of autoimmune disease or alloreactivity. They were also used in adoptive transfer experiments to study autoimmunity or induction of tolerance after xenogeneic thymus transplantation.1
Columns
For positive selection: MS, LS, XS, or autoMACS Columns. For depletion: LD, CS, D, or autoMACS Columns.
 
Figure 1
Isolation of T cells from rat spleen using Anti-T Cell (OX52) MicroBeads, a MidiMACS™ Separator, and an LS Column.
A: Spleen cells before separation
B: T cell-depleted fraction
C: Isolated T cells
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Products
Anti-T Cell (OX52) MicroBeads, rat
- for 109 total cells
Download datasheet
130-090-320
Qty.:
 

References
1. Yan et al. (2003) J. Immunol. 170: 5936-5946.
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