ibidi µ-Patterning Technology.
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Cell Image by J. Jatzlau & P.-L. Mendez, FU Berlin, Germany

Long-Term 3D Cultivation and Perfusion.
For Spheroids or Small Organoids.

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Simulate Physiological Systems.
For Single Cells, Spheroids, and Organoids.

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Where Precision Meets Performance.
Delivering Brilliant Microscopy.

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As Many Wells as You Need.
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Long-Term Live Cell Imaging.
On Every Inverted Microscope.

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Create an In vivo-like Extracellular Matrix.
For Live Cell Imaging in a 3D Environment.

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Image of the Month

2025 ibidi Calendar, September

Mari Angeles Juanes
Centre de Investigacio Principe Felipe, Valencia, Spain

Connecting with the cosmos: Mouse neurons were fixed and stained for F-actin (phalloidin, magenta), MAP2 (neurite marker, cyan), and nuclei (DAPI, yellow). The neurons were cultured in a μ-Slide 8 Well high, stained, and then imaged using a Leica wide-field DMi8 microscope with a 20x objective.

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