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Cell separation reagents Cell separation reagents
  for human cells
  for non-human primate cells
  for mouse cells
  Stem and progenitor cells
  Neural cells
  T cells
  NK cells
  B cells
  Monocytes and macrophages
  Myeloid derived suppressor cells
  Dendritic cells
  Antigen-presenting cells
  Granulocytes
  Leukocytes
  Endothelial cells
  Erythroid cells
  Cytokine-producing cells
  for rat 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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Pluripotent Stem Cell Isolation Kit
Overview
The Pluripotent Stem Cell Isolation Kit has been specifically designed for the depletion of early differentiated cells from mouse ES and iPS cell cultures. Based on a novel marker that discriminates between pluripotent and early differentiated cells, the kit guarantees the fast and easy isolation of homogeneous ES and iPS cell populations.
Details
Background information
Expression of markers, such as the transcription factors Oct-4 and Nanog or the surface carbohydrate SSEA-1 (CD15), are mainly used to characterize pluripotency of mouse cells on a molecular level. Nevertheless, expression dynamics of these markers are rather low, limiting their potential to discriminate between pluripotent and early differentiated cells. Our scientists have identified a cell surface marker that is strongly up-regulated during the early differentiation of mouse ES and iPS cells in culture. The novel Pluripotent Stem Cell Isolation Kit, mouse, was established on this basis and allows to easily deplete the early differentiated cells resulting in homogeneous pluripotent stem cell cultures.

Downstream applications
Depletion of early differentiated cells enables:

  • standardized pluripotent stem cell culture
  • standardized pluripotent stem cell differentiation experiments
  • profiling of pluripotent stem cells without contamination of differentiated cells
  • efficient generation of transgenic mice using pluripotent stem cells
Columns
LD or autoMACS Columns
Further information
ISSCR 2010_Removal of early differentiated cells from mouse pluripotent stem cell cultures by magnetic cell sorting
[PDF; 1,6 MB]
 
Figure 1
Mouse ES cell cultures containing 14% early differentiated cells (A), as they can occur during feeder-free cultivation, were separated using the Pluripotent Stem Cell Isolation Kit, an LD Column, and a MidiMACS™ Separator. Differentiated cells were completely removed resulting in a purity of approx. 99% pluripotent cells (B). Flow cytometric analysis using the MACSQuant® Analyzer. Debris and dead cells were excluded based on scatter signals and propidium iodide fluorescence.
A: Before separation
B: After separation
Figure 2
Phase contrast pictures of fixed feeder-free mouse embryonic stem cell cultures one day after plating without (A) and with separation (B) indicate efficient removal of differentiated cells.
A: Without separation
B: With separation
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Details
Products
Pluripotent Stem Cell Isolation Kit, mouse
- for 109 total cells
Download datasheet
130-095-267
Qty.:
 

Related products
Anti-SSEA-1 (CD15) MicroBeads, human and mouse (#130-094-530)
Mouse ES and iPS cell antibodies
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