
Atract™
Atract™ Kit is our T-cell activation reagent, consisting of biocompatible, metal-free particles with irreversibly bound anti-CD3, anti-CD28 and anti-CD2 antibodies, designed to interact with naive T lymphocytes and trigger their activation and expansion. We offer an improved version of the product, Atract™ Kit V2, which is further optimised for superior proliferation and a more user-friendly workflow.
The Atract™ Kit reagent was designed with our slogan and guidance in mind: “No magnets, no residuals just pure cells”. Reagent particles cannot be phagocytised and are easy to remove from the cell culture. Atract™ Kit is compatible with and scalable across conventional culture flasks, bags, plates and G-Rex platforms.
Atract™ Kit is offered in two different formats, adapted to different applications and scales of T-cell research. We are happy to advise and try to help tailor your Atract™ Kit experience to your unique needs, as well as provide you with additional knowledge and tips, based on years of research, development and optimization of our activation reagent.
Atract™ Kit V2 (50 mg)
Anti-CD2/-CD3/-CD28
Contents:
4x 50 mg of Bio-ReCell CD2/CD3/CD28 biocompatible particles
Contents of the kit are sufficient to activate up to 60 million peripheral blood mononuclear cells (PBMCs).
Atract™ Kit V2 (10 mg)
Anti-CD2/-CD3/-CD28
Contents:
4x 10 mg of Bio-ReCell CD2/CD3/CD28 biocompatible particles
Contents of the kit are sufficient to activate up to 12 million peripheral blood mononuclear cells (PBMCs).
For more information about the performance of the Atract™ Kits, download our information brochure.
Why Atract™
Data


Comparison of T-cell count between the Atract™ Kit and a market competitor after nine days of expansion in various scales of the G-Rex platform.
Proportions of T-cell subtypes for the Atract™ Kit and a market competitor product after 48h of activation.
FAQ
Which samples are appropriate for activation with Atract™?
Is Atract™ reagent removal necessary?
Which 20-35 μm strainers are suitable for filtering the suspension?
Can we use different protocols and adjust the official protocol?
Are there any requirements for cell culture containers?
Why does the protocol suggest adjustments for 96-, 48-, 24-, and 12-well plates?
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