LunaX™ TissueMatrix – Photocrosslinkable Extracellular Matrix

LunaX™ TissueMatrix is a tunable ECM tailored for 3D spheroid and co-culture models of mesodermal origin, including stromal and endothelial cell types.

Suitable for applications in oncology, vasculogenesis, and drug screening, LunaX™ TissueMatrix offers high reproducibility and intuitive handling—ideal for both expert users and researchers transitioning from 2D to 3D systems.

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Product Overview

LunaX™ TissueMatrix is a tunable ECM tailored for 3D spheroid and co-culture models of mesodermal origin, including stromal and endothelial cell types.

 

Suitable for applications in oncology, vasculogenesis, and drug screening, LunaX™ TissueMatrix offers high reproducibility and intuitive handling—ideal for both expert users and researchers transitioning from 2D to 3D systems.

 

LunaX™ TissueMatrix supports a wide range of mesodermal applications, including stromal and endothelial co-culture systems, vascular biology studies such as endothelial tube formation, and tumor–stroma interaction models.

 

Its stiffness can be finely modulated via visible light-mediated crosslinking, enabling the modelling of diverse physiological and pathological microenvironments. This makes LunaX™ TissueMatrix ideal for investigating processes such as tumor-stroma interactions, cellular invasion, and therapeutic responses.

 

Features

Tunable Stiffness Easy and Fast Biocompatible

Bioactive Motifs Consistent Quality Protease Degradeable

Kit Contents

Each kit conatins everything you need for precise, tunable 3D cell culture:
Low Stiffness Kit (0 – 6.5 kPa):
✔ 5 mL LunaGel™ ECM (2x solution)
✔ 5 vials of freeze-dried cytocompatible photoinitiator
High Stiffness Kit (0 – 25 kPa):
✔ 5 mL LunaGel™ ECM (1.5x solution)
✔ 5 vials of freeze-dried cytocompatible photoinitiator

 

How LunaX™ TissueMatrix Works

The LunaX™ TissueMatrix are tunable hydrogel systems engineered to enable precise modulation of ECM stiffness while preserving cellular viability and function.

 

Crosslinking is driven by a photoinitiator that undergoes activation upon exposure to cytocompatible blue visible light (λ = 405 nm), initiating a controlled polymerisation reaction. Stiffness can be incrementally increased by extending the duration of light exposure, allowing fine-tuned adjustment of the mechanical microenvironment. This approach facilitates the generation of physiologically relevant 3D models that recapitulate tissue-specific or disease-associated ECM mechanics, including progressive stiffening observed in tumorigenesis and fibrosis.

 

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