Magnetic cell separation nanobeads, CytoSinct™

Lieferant: GenScript Biotech
GENSL00864-1EA 524 EUR
GENSL00864-1 GENSL00863-1 GENSL00863-0.5 GENSL00864-0.5
Magnetic cell separation nanobeads, CytoSinct™
Zelltrennmedien
Efficient and gentle cell separation based on surface markers is essential for researching specific cell populations, and for developing life-saving cell and gene therapies. GenScript has renowned expertise in developing magnetic bead products for bioseparation of various types of biomolecules. The CytoSinct™ Cell Separation Technology uses perfected nanoparticle empowered immunomagnetic separation technology to isolate specific cell populations of interest, combining the specificity and sensitivity of antibody-based purification with the gentleness of nanoparticles and the ease and speed of magnetic separation.

  • Highly efficient
  • Biodegradable
  • Non-toxic
  • Compatible
  • Easy-to-use
  • Sterilised
  • Paramagnetic

The CytoSinct™ Cell Separation Manual Kit is composed of antigen specific paramagnetic Nanobeads, Columns, and magnetic Stands. The CytoSinct™ Nanobeads are nanometer-sized, easy-to-use, and enable highly efficient cell isolation.

CytoSinct™ Columns amplify the magnetic field and enable efficient separation with minimal labelling using the small beads.The separated cells are compatible with most downstream applications including cell culture, activation, expansion, flow cytometry analysis and translational research. Armed with the flexibility and specificity of the CytoSinct™ Cell Separation technology, you can use a variety of starting materials. Start with PBMCs or leukapheresis products. Enrich your target cells in your sample or deplete them.

For every experimental application, the CytoSinct™ Cell Separation technology can provide you with the separation results you require. Even more, CytoSinct™ Cell Separation Kit is compatible with other column-based cell separation platforms. Try this great tool to advance your research by simplifying your cell separation procedure.
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