ibidi GmbH develops, produces and distributes a "Lab-on-a-Slide" technology (so called µ-Slides) for the analysis of cells and biomolecules. At present, the product family covers cell culture µ-Slides, and protein µ-Slides. The cells can be seeded into a channel and conveniently be supplied with medium. The advantage of the µ-Slide is that it combines a cell culture dish with an optical observation chamber equivalent to the glass slide/cover slip setup that is required for high resolution microscopy. The simultaneous cultivation and optical analysis of the cells enables amongst othe.... Read more

Simulate physiological conditions: Mimic in vivo-like conditions for cells that ...

Stage Top Incubator for easy live cell imaging on every inverted microscope ...

Cells are imaged on a No. 1.5 ibidi Polymer Coverslip bottom with the highest op...

All-in-one 8 well chamber slide for cost-effective experiments with small cell n...

Provides in vivo-like extracellular matrix (ECM) structures Non-pepsinized, ...

ibidi GmbH develops, produces and distributes a "Lab-on-a-Slide" technology (so
called µ-Slides) for the analysis of cells and biomolecules. At present, the product
family covers cell culture µ-Slides, and protein µ-Slides.

The cells can be seeded into a channel and conveniently be supplied with medium.
The advantage of the µ-Slide is that it combines a cell culture dish with an optical
observation chamber equivalent to the glass slide/cover slip setup that is required for
high resolution microscopy.

The simultaneous cultivation and optical analysis of the cells enables amongst other
things; the use of immune fluorescence techniques, chemotactical investigations
and the simulation of blood vessels for adhesion and migration studies. The µ-Slide
channel can be completely coated with endothelial cells, for instance. Thus, the
µ-Slides provides a model system for interaction studies between blood stream and
vessel wall.
 
The high optical quality of the µ-Slide makes investigations with all usual microscopy
techniques such as DIC, phase contrast, confocal microscopy, Laser Scanning
Microscopy (LSM) and fluorescence correlation spectroscopy (FCS) possible.