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T cell stimulation & expansion

Key features:

CD3/CD28 Streptamers® for T cell expansion
CD3/CD28 Streptamers® for T cell
expansion

In contrast to other existing expansion systems,

  • with the CD3/CD28 Streptamers® for T cell expansion the stimulation of T cells can be stopped at any time point. You simply add D-biotin to the medium. The stimulation state of the cells can thus be precisely controlled;
  • with the Streptamer® CD3/CD28 Kit for T cell expansion you can modify the CD3 : CD28 Fab-Strep® ratio according to your needs, or you follow our recommendations;
  • with the Streptamer® CD3/CD28 Premix for T cell expansion you can benefit from a quick protocol with ready-to-use reagents.

Get unmanipulated naturally occurring T cells for your research with the Streptamer® technology!

Workflow for cell expansion

T cell stimulation

Naive T cells require at least two signals for activation, proliferation and differentiation. The first signal is generated via the T cell receptor (TCR) and its MHC ligand. The second, most effective co-stimulatory signal is evoked by the interaction of the CD28 receptor of the T cell with its ligand CD80/86 (glycoprotein B7).

CD3/CD28 Streptamers® for T cell expansion

The in vitro generation of a large number of functional T cells is important for basic research as well as for therapeutic approaches. Commonly used stimulatory reagents for resting T cells are magnetic beads carrying αCD3 and αCD28 monoclonal antibodies.

The Streptamers® for cell expansion are novel reagents for polyclonal expansion of T cells:

They are non-magnetic soluble protein complexes generated by multimerization of αCD3- and αCD28 Fab-Streps with a Strep-Tactin® multimer.
They are completely reversible reagents, i.e. they can be removed from the cells by the addition of biotin.

Reaction scheme of CD3/CD28 Streptamers® for T cell expansion

CD3- and CD28 Fab-Streps are multimerized via the soluble Strep-Tactin® multimere to generate the soluble Streptamer® for cell expansion. The subsequent biotin-induced dissociation of the reagents from the cells can be performed at any time point during stimulation, simply by the addition of biotin. The termination of stimulation can thus be precisely controlled.