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DyNAtrix® - 3D cell culture matrix

Fully synthetic, xeno-free. 
Designed to make 3D cell culture easy. 

DyNAtrix is a synthetic hydrogel for 3D cell culture and organoids. No animal-derived components, no undefined growth factors, no lot-to-lot variation. Embed cells easily, image directly in the gel, and dissolve cleanly when you're ready to harvest.

DyNAtrix® at a glance

Validated across cell lines, primary cells, and organoid models by ~20 pilot users and collaborators.

Want to join our growing force of early adopters? Try our pilot kits.

DyNAtrix Ready-to-Use Kit

Ready-to-Use Kit

Cells
iPSCsMSCsMDCKChondrocytes
Organoids
PlacentaKidneyBrain
Tumoroids
MDA-MB-231
breast cancer
MCF-10A ER-Src
breast (inducible model)
KG-1
leukemia
Glioblastoma
brain cancer

Don't see your cell type or organoid? Get in touch about custom validation.

See the published data →

What makes DyNAtrix unique and powerful

Chemically defined

Xeno-free & synthetic. Aligns with NAMs initiative and supports animal-free research.

Similar to traditional workflow

Simple protocol mimicking
traditional matrix handling. Quick
adaptation to your exsiting
workflow.

Simple & gentle cell release

Harvest cells gently while
maintaining high vaibility at 37°C for 30 min in cell culture medium .

Optically transparent

DyNAtrix is compatible with fluorescent microscopy, confocal, and light-sheet imaging.

Independently tunable

Unprecedented control over stiffness and viscoelastic properties 

Bioprintable

Self-healing and injectable. Suitable for extrusion printing as bio-ink.

Reproducible

Guaranteed batch-to-batch consistency. One less thing to worry about. 

Long term shelf stable

DyNAtrix is stable for long-term cell culture (> 60 days), and storage at 4°C for > 6 months.

Permeable

Low fouling and highly permeable for antibody staining in gels.

A four-step workflow. Familiar from the start.  

Designed to fit into your existing 3D culture setup. Same steps as basement membrane matrices.

But, with better-defined chemistry underneath.

Step 1: Mix precursors & cells

Step 2:Incubate at 37°C

Step 3: Culture and image

Step 4: Release cells (optional)

Mixing and gelation

DyNAtrix precursors exhibit a liquid-like consistency prior to mixing. Hydrogel formation is initiated by combining precursor B+ with precursor X, followed by incubation at 37°C. This procedure is designed to closely resemble standard animal-derived matrix protocols.


Imaging and analysis
Hydrogels can be imaged directly during ongoing culture. Alternatively, fixation and staining procedures can be performed within the hydrogel matrix without prior cell recovery.


Cell release

DyNAtrix hydrogels can be gently degraded in cell culture medium at 37°C using DNase I, enabling the recovery of cells with high viability for downstream analyses or subsequent passaging.

Works in the vessels you already use

DyNAtrix is flexible. Use it in your existing labware without adapting your setup.

Validated across a wide range of cell types and organoids

Tested in the following human and mammalian systems. Don't see yours? That's what the pilot programme is for.

Kidney Cysts

iPSCs

Placenta organoids

Mesenchymal Stem cells

Advance your research with our pilot kits  

Two kits to get you started. Both include protocols and direct support from our team. 

Ready-to-use kit

✓ Ready to mix with cell suspension. No extra prep

✓ Supports wide range of cell types and vessels

✓ Protocol analogous to traditional matrix handling

✓ Stable at 4°C for > 6 months

Minimal discovery kit

✓ Adjust stiffness and stress relaxation between cultures
✓ Investigate how cells respond to mechanical conditions      
✓ Create optimal matrix conditions for your cell system
✓ Ideal for mechanobiology and precision organoid research

Bonus features

Switchable stress-relaxation crosslinkers

Change stress relaxation properties between cell culture conditions without re-embedding.

Fluorescence force sensors

Visualise cell-generated forces directly in 3D hydrogels using built-in fluorescent tension probes.