The truly biological barrier model

Biological membrane for biomimetic cell culture

Familiar format for easy handling

Optically clear for in situ imaging

Familiar Form, Revolutionary Function

  1. 1. Seed Cells
  2. Seed cells onto either side of the membrane

  1. 2. Culture & Monitor
  2. Monitor in situ with brightfield & fluorescence microscopy

  1. 3. End Point Analysis
  2. Easy cryosectioning or cell removal for analysis like FACS or RNA isolation

The Membrick works with your existing workflow and assays, but it offers the ability to monitor cells in situ during culture using inverted brightfield or fluorescent microscopy, saving time, cells, and replicates.

Live Imaging

HPVECs in culture on Membricks. Top: In situ brightfield imaging. Bottom: In situ immunofluorescent imaging with CD31 staining (endothelial marker) on day 12 on Membrick vs. plastic (PET) cell culture inserts. Scale bars 100 μm. Kreuder et al., 2020. CC4.0.

The optically clear membrane allows for in situ imaging of cells in culture. This provides an alternative to performing end-point analysis at each time-point, reducing the number of replicates, cells, and the time needed for experimentation.

The Membrick is fully compatible with ubiquitously available inverted microscopes, unlocking high-throughput applications.

Barrier Formation

BeWo (placental cell line) and HVMF (placental fibroblasts) in mono- and co-culture over 7 days. Left: transepithelial/transendothelial electrical resistance (TEER). Right: Permeability rate of lucifer yellow through the membrane and cell layers. Kreuder et al., 2020. CC4.0.

TEER Measurements

Results show that the co-culture of BeWo and HVMF cells exhibits a stronger barrier formation than the sum of either cell type in monoculture, demonstrating the power of the Membrick for co-culture models.

Permeability Assays

In a culture containing BeWo cells (which are expected to be responsible for barrier formation) the permeability rate of lucifer yellow is dramatically lower. A co-culture with HVMFs further reduces permeability.

End-Point Analysis

Top: HPVECs stained for von Willebrand factor and CD31 (endothelial markers) on day 12, scale bar 100 μm. Middle: BeWo (placental line) stained for β-catenin (cell-cell adhesion) on day 5, scale bar 50 μm. Bottom: HPVECs stained for vascular endothelial cadherin (tight junctions), scale bar 25 μm. Kreuder et al., 2020. CC4.0.

Cryosectioning and Staining

Easily cryosection and perform (immuno)histological staining on the biological membrane.

In the top and bottom images here, more robust endothelial marker and tight junction expression can be seen on the Membrick's biomimetic membrane, as compared to a plastic (PET) cell culture insert.

Cell Removal & Analysis

Remove cells via trypsinization for endpoint analysis (FACS or DNA/RNA isolation/sequencing).

Compatible with Existing Assays

Barrier Evaluation

Permeability Assays

Transepithelial/transendothelial electrical resistance (TEER)


Brightfield Microscopy

Fluorescent Microscopy

Confocal Microscopy

Two Photon Microscopy

Cell Analysis

RNA/DNA Sequencing


Metabolic Assays