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CD105 MultiSort Kit (PE)
Overview
The CD105 MultiSort Kit (PE), mouse has been developed for the isolation of CD105+ cells or cell subsets, including
  • vascular endothelial cells from mouse tissue or cell cultures
  • long-term repopulating hematopoietic stem cells (LTR-HSCs) from mouse bone marrow when used in combination with the Anti-Sca-1 MicroBead Kit (FITC).
Details
Background information
CD105, also known as Endoglin, is abundantly expressed on angiogenic endothelial cells. In mouse bone marrow, CD105 is also expressed on a subpopulation of Sca-1+ hematopoietic stem cells that displays long-term repopulating activity in lethally irradiated mice (LTR-HSCs)1.

Detailed separation procedure
In the first step, CD105+ cells are positively selected after labeling with the CD105 MultiSort MicroBeads. Subsequently, the MultiSort MicroBeads are enzymatically released from the CD105 antibody. The selected CD105+ cells can be magnetically labeled and sorted according to a second antigen. The kits contains CD105 MultiSort MicroBeads, MultiSort Release Reagent, and the MultiSort Stop Reagent.

Downstream applications
Isolated CD105+Sca-1+ cells can be transplanted into lethally irradiated mice to evaluate the long-term engraftment potential of this cell population.
Columns
MS, LS, or autoMACS Columns.
Further information
Isolation of CD105+Sca-1+ LTR-HSCs from mouse bone marrow
[PDF; 192,3 KB]
 
Figure 1
Isolation of CD105+Sca-1+ LTR-HSCs from mouse bone marrow using the CD105 MultiSort Kit (PE), mouse, and two LS Columns for the first positive selection followed by the Anti-Sca-1 MicroBead Kit (FITC), mouse, and two MS Columns in the second positive selection step.
A: Before separation
B: CD105+ cells
C: CD105+Sca-1+ LTR-HSCs
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Details
Products
CD105 MultiSort Kit (PE), mouse
- for 109 total cells
Download datasheet
130-092-924
Qty.:
 

Related products
Anti-Sca-1 MicroBead Kit (FITC), mouse (#130-092-529)
Lineage Cell Detection Cocktail-Biotin, mouse (#130-092-613)
References
1. Chen et al. (2002) Proc. Natl. Acad. Sci. USA 99: 15468–15473.
2. Chen et al. (2003) Immunity 19: 525–533.
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